meid 936 neuroscience laboratory syllabus · 2020. 9. 22. · meid 608 neuroscience laboratory...
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MEID 608
NEUROSCIENCE LABORATORY SYLLABUS
BY
JOHN B. GELDERD, Ph.D.
The illustrations within the text of this laboratory syllabus were created by Joan Quarles. Selected
illustrations within the syllabus were modified from published illustrations by Frank Netter, MD
with the permission of Novartis Medical Education, Whippany, NJ.
Neuroscience Laboratory Manual 2
TABLE OF CONTENTS
Lab Date Laboratory Session Pages
Exam 1
1 January 3rd Gross Anatomy of the Brain 6 – 13
2 January 4th
Meninges 14 – 16
Blood Supply 17 – 22
CSF and Ventricles of the Brain 23 – 26
3 January 7th Introduction to the Macroscopic Anatomy of the
Neuraxis 27 – 32
4 January 8th Ascending Sensory Pathways 33 – 36
Sensory Pathways for the Anterior 2/3 of the Head 37 – 39
Exam 2
5 January 14th Pyramidal System 40 – 43
6 January 16th Cranial Nerves 44 – 52
Neuroround 53
7 January 17th Basal Ganglia 54 – 58
Neuroround 59
8 January 18th Cerebellum 60 – 67
Neuroround 68
Exam 3
9 January 30th Vestibular System 69 – 70
Auditory System 71 – 73
10 January 31st Visual System 74 – 77
11 February 1st Diencephalon (Hypothalamus) 78 – 81
Limbic System 82 – 87
12 February 4th Cortex and Review 88 – 93
Neuroround 1 – 2 94 – 97
Labeled Slides from Slide Set 98 – 116
Neuroscience Laboratory Manual 3
INTRODUCTION
The purpose of this syllabus is to assist and guide the student through the
neuroscience laboratory portion of Neuroscience (MEID 608) in a systematic
fashion. It has been prepared specifically for the curriculum at the Texas A&M
University College of Medicine. The ultimate goal of the laboratory portion of this
course is to provide a "hands on" experience in learning and understanding the
FUNCTIONAL anatomy of the human central nervous system (CNS).
To assist you in this endeavor, this syllabus will be used in conjunction with the
following laboratory materials:
1. The Medical Neuroscience Laboratory Manual (downloaded from eCampus
under MEID608 Neuroscience). This file contains the Neuroscience Manual
& Slide Set.
2. Two Brain Buckets (shared by a MDL group) containing:
#: Whole and Half Brain
#A: Horizontally and Coronally Sectioned Brains
3. An Atlas of Neuroanatomy. Each laboratory group will receive one copy of
the “Atlas of the Human Brain and Spinal Cord” (Fix, J., 2nd ed.). It is strongly
recommended that your laboratory group use your atlas in each laboratory
session. Moreover, it will be of value in all phases of this course to help you
in understanding the three-dimensional anatomy of the human nervous
system.
There is also an additional item that should be downloaded from eCampus. This
includes a set of annotated Neuroscience slides (Neuroscience Lab Manual
Supplement). The file of labeled slides contains representative spinal cord and
brainstem sections taken from your slide set.
Neuroscience Laboratory Manual 4
NOTE: UNDER NO CIRCUMSTANCES ARE THE BRAIN SPECIMENS TO BE REMOVED
FROM THE LABORATORY AT ANY TIME.
To assist you in learning the neuroanatomical structures discussed in this
laboratory manual, there is an “Objectives” statement at the beginning of each
laboratory section. Further, the important structures and/or concepts for each
laboratory are in bold print or are underlined. In addition, questions pertinent to
the area being studied are interspersed throughout each laboratory session in
italicized print.
For examination purposes, the location of neuroanatomical structures will be
assessed from lecture and the laboratory manual. Lecture handouts and the
laboratory manual are considered the ultimate authority in correctly identifying
structures and the determination of correct answers for exam questions. As such,
contradictory information obtained from external resources (other atlases,
websites, annotated slides from your preceding classmates) does not apply.
Animations – For many laboratory assignments in this manual, links to video
animations are provided. These animations depict the anatomical relationships
between important (bold) structures that will assist in your understanding of
the three-dimensional organization of the brain.
Laboratory Demonstrations -- There will be laboratory demonstrations during
most laboratory sessions. These will consist of models and/or pre-dissected wet
specimens. Since these demonstrations will be "fair game" for laboratory
practical exams, it is recommended that you take the time to view them when
they are displayed during normal laboratory hours.
Neurorounds – For some laboratory sessions, case studies will be used to
integrate lecture and lab material so as to illustrate their clinical implications.
These case studies will be administered using two different formats: 1) active
learning presentation/discussion in lab; or 2) self-study, written with
corresponding questions. Active learning case studies (#1) will be presented by
faculty usually during the last 30-40min of lab. Students will be expected to
review the lab and associated lecture in advance so as to enable participation in
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the discussion and provide “team-based” responses to questions on pathways
and clinical correlates related to the case. Self-study written cases (#2) are
provided at the end of corresponding labs. Students should review the case
study in advance and begin working on the case during the lab. Each case
contains questions about related pathways/function and specific clinical
findings. Faculty will be available during the lab to discuss/clarify clinical findings
and other aspects of the case but not provide answers to the questions. Answers
to these questions will be posted ~2 days after the lab on eCampus. Although
there are no specific performance-type grades for the active learning or self-
study written case studies, the content of these cases will be covered in some
fashion on either the practical or written exams and related questions should
be expected on the NBME and USMLE exams.
Finally, it will be useful to read through each laboratory assignment, using your
brain atlas, prior to the laboratory session. This should help make both lecture and
laboratory material easier to comprehend.
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GROSS ANATOMY OF THE BRAIN
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Utilize their developing anatomical vocabulary to locate and identify external and internal features of the brain.
2. Describe the directional terminology of the central nervous system (CNS) and the location where this terminology axis shifts.
3. Discuss the major subdivisions of the brain and key anatomical structures located within these regions.
4. Demonstrate gray and white matter and relate the specific cellular parts (cell body vs. axons/dendrites) constituting the two.
5. Identify the lobes of the brain, landmarks demarcating their separation and general features of each.
___________________________________________________________________
Before we begin, it is important to understand the directional terminology or
nomenclature as it relates to the brain. Below is a diagram (Fig. 1) to assist you in
understanding this terminology. It is important that you understand it, since we
will be using this terminology in lecture and laboratory throughout the course to
describe the relative locations of various CNS structures.
Neuroscience Laboratory Manual 7
In this laboratory session, we will be studying what could be called "lump and
bump" anatomy. That is, we will be identifying and briefly discussing the gross
external and internal anatomy of the brain. The purpose of this laboratory is
simply to acquaint you with the appearance and location of structures that we
will be revisiting in detail as the course progresses. These structures will also be
used as landmarks to locate and identify other anatomical features of the brain.
Use your atlas to assist in the identification of the structures listed in this and all
future laboratory sessions.
Whole and Half Brain Specimens
We will begin by identifying the features of the major subdivisions of the brain,
using the whole and half brain specimens in your brain buckets. The brain is
organized from rostral to caudal as follows: 1) telencephalon, 2) diencephalon, 3)
mesencephalon [midbrain], 4) metencephalon [pons], 5) myelencephalon [medulla
oblongata] and 6) cerebellum. Items 2 through 5 above are collectively called the
brainstem.
The telencephalon is composed of the cerebral hemispheres and portions of the
basal ganglia. The latter will be studied in a subsequent laboratory session. The
cerebral hemispheres are the large, external, convoluted mantles of nervous tissue
that overlie the brainstem. The superficial region of the cerebral hemispheres is
composed of gray matter. Immediately deep to the gray matter is a relatively thick
layer of white matter. To confirm this, look at selected horizontal and coronal
sections. How does this compare to what is seen in spinal cord? The cerebral
hemispheres are divided into right and left halves at the midline by the prominent
interhemispheric (longitudinal cerebral) fissure. The raised areas, or convolutions,
on the surface of the cerebral hemispheres are called gyri (sing. - gyrus). The
corresponding grooves or depressions are collectively called sulci (sing. - sulcus).
The larger, deeper grooves are usually referred to as fissures.
Each cerebral hemisphere is divided into lobes (Fig. 2). Observe the brain from a
lateral view. From this perspective, it resembles a catcher's mitt with the "thumb"
portion located in a ventrolateral position. This "thumb" portion is the temporal
lobe. It is separated from the more dorsal aspect of the brain by a deep groove
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called the lateral (Sylvian) fissure. Locate the horizontally arranged superior,
middle and inferior temporal gyri. Immediately dorsal to the lateral fissure is the
frontal lobe, which extends from the rostral pole (end) of the brain caudally to the
central sulcus (of Rolando). This sulcus separates the frontal lobe from the parietal
lobe. Two important gyri lie immediately rostral (precentral gyrus) and caudal
(postcentral gyrus) to the central sulcus. Immediately rostral to the precentral
gyrus is the precentral sulcus. Rostral to the precentral sulcus lie three horizontally
arranged gyri. These are, from dorsal to ventral, the superior, middle and inferior
frontal gyri.
The caudal extent of the parietal and temporal lobes is delineated by an imaginary
line drawn from the parietooccipital sulcus dorsally to the preoccipital notch
ventrally (Fig. 2). The remaining region of brain from the "imaginary line" caudally
is called the occipital lobe. The caudal-most extent of the occipital lobe is called
the occipital pole. The parietal lobe is separated from the temporal lobe by
drawing an imaginary horizontal line that extends caudally from the Sylvian fissure
to the previous "imaginary line" between the parietooccipital sulcus to the
preoccipital notch.
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The caudal end of the Sylvian fissure turns dorsally to terminate and is surrounded
by the supramarginal gyrus. Deep to the Sylvian fissure lies a region of cortex called
the insula (insular cortex [lobe]). Identify this structure on your horizontal and
coronal brain slices. In some instances, the insula can be seen on the whole or half
brain by GENTLY separating the frontal and temporal lobes. If you are unable to
see the insula on your whole or half brain specimens, this structure can be seen
clearly on demonstration. DO NOT FORCE THE LOBES APART BY TEARING BRAIN
TISSUE.
Now turn the whole brain over to view the ventral surface. Beginning on the lateral
aspect of the temporal lobe and working medially, find the occipitotemporal
(fusiform) gyrus, and parahippocampal gyrus. Near the rostral end of the
parahippocampal gyrus is a small, medially directed protuberance of cortical tissue
called the uncus.
To complete our survey of the cerebral hemispheres, observe the medial surface
of the half brain. Find the central sulcus as it winds its way onto the dorsal aspect
of the medial surface of the cerebral cortex to terminate. Surrounding the
termination of the central sulcus is the paracentral lobule, which is a fusion of pre-
and postcentral gyri. Immediately caudal to the paracentral lobule is a region of
cortex called the precuneus. It is bounded caudally by the vertically oriented
parietooccipital sulcus. From the occipital pole, the calcarine sulcus runs rostrally
to join the parietooccipital sulcus. The calcarine sulcus divides the occipital lobe
into a dorsal region called the cuneus and a ventral region called the lingula.
Located at the approximate center of the medial surface of the half brain is a sickle
shaped structure, the corpus callosum. This is a massive interhemispheric nerve
fiber pathway that provides reciprocal communication between the two cerebral
hemispheres. It is divided into parts from rostral to caudal as follows: rostrum,
genu, body and splenium. The corpus callosum is surrounded by cerebral cortex
that contributes to a structure we will study in detail later called the limbic lobe.
Hanging from the ventral surface of the corpus callosum is a membrane called the
septum pellucidum. Along the free ventral border of the septum pellucidum is a
fiber bundle called the fornix. Follow the fornix as it arches rostrally. In the region
just rostral to where the fornix dives out of site is a small interhemispheric fiber
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bundle called the anterior commissure. This structure interconnects portions of
the temporal lobes and components of the olfactory system. Immediately rostral
and ventral to the anterior commissure is a thin membrane called the lamina
terminalis. This structure spans the midline. As such, it has been cut on your half
brain specimens. Follow the lamina terminalis ventrally to the optic chiasm. Note
that the optic chiasm is continuous with the optic nerves (CN II) rostrally and the
optic tracts caudally. Just ventral to the optic chiasm is the infundibulum (pituitary
stalk). Arching caudally from this structure is another thin sheet of tissue called
the tuber cinereum, which leads to the paired mammillary bodies. (NOTE: since
you are viewing the half brain, there will be only one mammillary body). The region
of brain roughly between the lamina terminalis and the caudal aspect of the
mammillary bodies is the hypothalamus. It is separated from the dorsally located,
egg-shaped thalamus by a rostrocaudal groove called the hypothalamic sulcus.
On the half brain, the medial surface of the thalamus typically reveals a severed
medial protrusion of thalamic tissue. This is the remnants of the massa intermedia
(interthalamic adhesion) which, when present, connects the left and right thalami.
The hypothalamus, thalamus, habenula and pineal gland constitute the major
portion of the diencephalon, the most rostral extent of the brainstem. Another
structure, the subthalamus, is also a part of the diencephalon and will be seen at a
later date. It should be noted at this point that there is a space between
diencephalic structures on the left and right sides. This centrally located space is
the third ventricle.
At the juncture of the thalamus and midbrain (mesencephalon), there is a ventral
flexure of the brainstem. This is called the cephalic flexure. Proceeding caudally
(inferiorly) from the mammillary body on the half brain, there is a relatively deep
longitudinal furrow in the midline. This is the interpeduncular fossa. Just lateral
to the interpeduncular fossa, observe one of the paired cerebral peduncles (crus
cerebri). These are important structures that carry descending nerve fibers from
the cerebral cortex to other regions of the brain and spinal cord. If intact, the
oculomotor nerve (CN III) can be seen emerging from the medial surface of the
cerebral peduncle. On the dorsal surface of the midbrain lie two rounded
protuberances. The more rostral one is the superior colliculus, which is associated
with the visual system. The more caudal one is the inferior colliculus, which is
associated with the auditory system. On the whole brain, each of these colliculi are
Neuroscience Laboratory Manual 11
paired structures (i.e., two superior colliculi, two inferior colliculi [see
demonstration]) and are collectively referred to as the corpora quadrigemina or
tectum of the midbrain. Separating the tectum and the more ventrally located
tegmentum of the midbrain is a small rostro-caudal channel called the cerebral
aqueduct (of Sylvius).
The large ventral convexity caudal to the cerebral peduncles is the pons
(metencephalon). If an imaginary line is drawn from the inferior aspect of the
inferior colliculus ventrally to the junction of the cerebral peduncles with the pons,
this roughly represents the caudal extent of the midbrain. Follow the pons
dorsolaterally. Just caudal to where the trigeminal nerve (CN V) emerges, there is
a thick band of nerve fibers connecting the pons with the overlying cerebellum.
This is the middle cerebellar peduncle (brachium pontis). (NOTE: there are also
inferior and superior cerebellar peduncles that can be seen on demonstration).
The "potbellied" pons ends caudally where it meets the medulla (myelencephalon)
at the ponto-medullary junction. This can be seen as a horizontal groove from
which the abducens (CN VI), facial (CN VII) and vestibulocochlear (CN VIII) nerves
emerge from medial to lateral respectively. The lateral-most portion of this groove
where CNs VII and VIII emerge is called the cerebellopontine angle. This is where
the pons, medulla and cerebellum join together. The large cerebellum can be seen
sitting astride the dorsal surfaces of the pons and medulla. Two thin sloping
membranes (superior & inferior medullary vellae) usually can be seen stretching
between the cerebellum and the dorsal surface of the brainstem. The superior
medullary velum (more rostral) and the inferior medullary velum (difficult to see
but stretches from the inferior aspect of the cerebellum to the medulla) form a
triangular space with the pons and medulla, called the fourth ventricle.
The ventral surface of the medulla is best seen on the whole brain. On either side
of the midline on the medulla, just caudal to the ponto-medullary junction, is a pair
of rounded ridges. These are the pyramids and are caused by the underlying
pyramidal (corticospinal) tract. Immediately lateral to the pyramids at this level are
a pair of egg-shaped swellings called the inferior olives. The groove between the
inferior olive and the pyramid on each side is the preolivary sulcus. Filaments of
the hypoglossal nerve (CN XII) can be seen emerging from this sulcus. Dorsolateral
to the inferior olive is another groove called the postolivary sulcus from which the
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glossopharyngeal (CN IX), vagus (CN X) and the bulbar portion of the spinal
accessory (CN XI) nerves emerge.
Identify the following structures on the whole brain: lamina terminalis, optic
nerves, optic chiasm, optic tracts, infundibulum, tuber cinereum, mammillary
bodies, cerebral peduncles, interpeduncular fossa, CN III, pons, CN V, VI, VII and
VIII, middle cerebellar peduncles.
ANIMATIONS
Cerebral cortex - lobes (BrainlobesX, BrainlobesY)
Brainstem
DEMONSTRATIONS
Dorsal brainstem showing: thalamus, superior and inferior colliculi,
trochlear nerve (CN IV), superior, middle and inferior cerebellar peduncles,
fourth ventricle. Use Fig. 3 below to assist in identifying the above structures
on the demonstration.
Neuroscience Laboratory Manual 13
Half brain (lateral view) showing: central sulcus, lateral fissure, precentral
and postcentral gyri, insula, paracentral lobule, angular gyrus,
supramarginal gyrus.
Half brain (medial view) showing: paracentral lobule, parietooccipital
sulcus, calcarine sulcus, lingula, cuneus, corpus callosum (all parts),
cingulate gyrus.
Neuroscience Laboratory Manual 14
MENINGES
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Review the layers of meninges as learned in Gross Anatomy.
2. Locate and be able to name the subarachnoid cisterns which surround the brain and spinal cord.
___________________________________________________________________
The meninges consist of 3 concentric membranous layers of tissue that surround
the brain and spinal cord.
Dura mater -- The outermost, thick, fibrous layer of meninges is called the dura
mater. As many of you know from gross anatomy, the dura mater is made up of 2
layers (an inner [meningeal] and outer [endosteal/periosteal] layer) that are
typically fused together. The outer layer is, in turn, fused to the inner surface of
the skull. As such, there will not be any dura mater on the brains in your buckets.
It should be noted that the periosteal layer of dura mater passes through the
foramen magnum to fuse with the periostium on the external surface of the skull.
Consequently, the only layer of dura mater covering the spinal cord is the
meningeal layer. Since the dura mater is intimately involved in the drainage of
blood from the brain, there will be a demonstration of the dura mater and its
reflections within the skull later in this laboratory session during our review of the
blood supply to the CNS.
Arachnoid mater -- This intermediate layer of the meninges usually remains at least
partially intact on the surface of the brain after it is removed from the skull. On the
whole or half brain, look on the lateral surfaces of the cerebral hemispheres. If the
arachnoid mater is present, it will appear as a transparent membrane that spans
the sulci and fissures of the cerebral cortex. Immediately deep to the arachnoid
mater lies an important region called the subarachnoid space. It contains: 1)
cerebrospinal fluid and 2) the major blood vessels of the brain. Using a blunt probe,
slip the tip through an existing gap or tear in the arachnoid mater and gently elevate
Neuroscience Laboratory Manual 15
the arachnoid layer to demonstrate the subarachnoid space. Over most of the
surface of the brain, the subarachnoid space is relatively shallow. However, in
those regions where there are wide and/or deep depressions on the surface of the
brain, the arachnoid layer stretches across these depressions, resulting in
enlargement of the subarachnoid space. These enlargements are called
subarachnoid cisterns.
Using both the whole and half brains, four of the major cisterns can be
demonstrated. On the ventral surface of the midbrain, locate the cerebral
peduncles. The depression in the midline between the cerebral peduncles is the
interpeduncular fossa. If the arachnoid is present, it will be seen stretching across
the interpeduncular fossa between the cerebral peduncles. The space formed
between the floor of the fossa and the overlying arachnoid layer is called the
interpeduncular cistern. Immediately caudal to the cerebral peduncles lies the
convex protuberance of the ventral pons. The pontine cistern lies immediately
ventral to the pons and extends caudally to enlarge and terminate at the junction
of the pons and medulla (ponto-medullary junction). Now turn the brains over to
view the dorsal surface. The two cisterns on this surface of the brain lie either
immediately rostral or caudal to the cerebellum. The more rostral of these, the
superior cerebellar (quadrigeminal) cistern is best seen on the medial surface of
the half brain. It is roughly bounded by the splenium of the corpus callosum
superiorly, the superior and inferior colliculi (corpora quadrigemina) ventrally and
the superior surface of the cerebellum inferiorly. The remaining cistern of note,
the cerebellomedullary cistern (cisterna magna), lies at the inferior surface of the
cerebellum and the dorsal surface of the medulla where the arachnoid layer
reflects from the cerebellum to the medulla. Use your blunt probe to gently
explore the extent of these cisterns. It is important to note that another clinically
important cistern is located immediately caudal to the termination of the spinal
cord. What is the name of this cistern? At what vertebral level does the spinal cord
terminate?
Pia mater -- This innermost layer of the meninges is, for the most part, closely
adhered to the surface of the brain and spinal cord. As such, it is difficult to
demonstrate with the naked eye. At the microscopic level, small blood vessels that
penetrate the parenchyma (substance) of the brain are surrounded by pial sleeves
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that penetrate variable distances into the brain. There are two obvious occasions
where the pia mater separates from the surface of the CNS and can be readily seen.
What is the site of each of these pial separations and what are they called? (Think
Gross Anatomy).
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BLOOD SUPPLY TO THE BRAIN AND SPINAL CORD
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Identify the main arteries supplying the brain, brainstem and spinal cord.
2. Describe the areas of the central nervous system supplied by specific arteries.
3. Name the component parts and function of the Circle of Willis.
4. Discuss the general level of dysfunction that would result from compromise of any of the described vessels.
5. Identify watershed areas which correspond to border zones between the territories of two principle arteries.
6. Review the dural venous sinuses and trace the major veins that drain the CNS.
___________________________________________________________________
Vascular injury and/or vascular disease constitute a major source of nervous
system pathology. The CNS is critically dependent upon glucose and oxygen,
neither of which is stored in significant amounts by the CNS. Consequently, should
the blood supply to the CNS be disrupted, even for a relatively brief period,
destruction of CNS parenchyma occurs with the resultant permanent loss of
function, or death.
Brain -- The blood supply to the brain is typically described as being provided by
two arterial systems: an anterior system which is composed of the internal carotid
arteries and their branches; and the posterior (vertebral - basilar) system,
composed of the vertebral arteries. These two systems are demonstrated in Fig. 4
below.
Neuroscience Laboratory Manual 18
Posterior System -- Using the whole brain, turn it over to view the ventral surface.
Note the paired vertebral arteries ascending on the ventrolateral surface of the
medulla. As you may recall, the vertebral arteries arise from the subclavian arteries
and ascend through the foramina transversaria of cervical vertebrae C-6 through
C-1 to enter the skull through the foramen magnum. Typically, the vertebral
arteries fuse at the midline at the level of the ponto-medullary junction to form
the unpaired basilar artery. Before the vertebral arteries fuse, they give rise to
three pairs of arteries. The first of these are the posterior spinal arteries that
descend on the dorsal surface of the spinal cord just medial to the dorsal spinal
roots. Since the posterior spinal arteries are typically the first to arise from the
vertebral arteries as they traverse the foramen magnum, they are often absent due
to the level where the vertebral arteries were cut when the brain was removed
from the skull. The second branches are the posterior inferior cerebellar arteries
(PICA) which wrap around the medulla to ramify on the inferior surface of the
cerebellum. As these arteries wrap around the medulla to gain access to the
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cerebellum, they send small branches to supply the lateral region of the medulla.
Occasionally, the posterior spinal arteries may arise from PICA. The anterior spinal
arteries, which descend to fuse as a single artery at the midline on the ventral
surface of the medulla, are usually the last branches from the vertebral arteries
before they fuse to become the basilar artery. Shortly after the basilar artery is
formed, it gives rise to the paired anterior inferior cerebellar arteries (AICA), which
ramify on the ventral surface of the cerebellum. As the basilar artery ascends on
the ventral surface of the pons, it gives rise to many small pontine arteries. Just
prior to terminating, the basilar artery gives rise to the paired superior cerebellar
arteries, which wrap around and supply the midbrain on their way to ramify on the
superior surface of the cerebellum. The basilar artery terminates at the level of the
midbrain by dividing into the large, paired posterior cerebral arteries. At this time,
look for the oculomotor nerve (CN III) which acts as a landmark by emerging
between the posterior cerebral and superior cerebellar arteries.
Anterior System -- After entering the skull through the carotid canal each internal
carotid artery passes through the cavernous sinus, then turns 180° caudalward to
gain access to the ventral surface of the brain. It is at this point that the internal
carotid arteries are cut to remove the brain from the skull. On the ventral surface
of the whole brain, find the severed ends of the internal carotid arteries as they lie
just lateral to the optic chiasm. There are four branches that can be readily seen
arising from the internal carotid arteries: two from the main trunk and two terminal
branches. The first small branch is the posterior communicating artery. This artery
passes caudally to anastomose with the posterior cerebral artery. The next branch
is the anterior choroidal artery. This small artery passes caudally to disappear deep
to the temporal lobe. As the name implies, this artery supplies blood to the choroid
plexus (and other structures). Shortly after the internal carotid artery gives rise to
the anterior choroidal artery, it divides into its two terminal branches, the anterior
and middle cerebral arteries. The latter is larger and considered by some to be the
continuation of the internal carotid artery. Immediately distal to the origin of the
anterior choroidal artery, a variable number (2-5) of small threadlike arteries can
be seen arising from the middle cerebral artery and immediately diving into brain
parenchyma. These are the lateral striate (lenticulostriate) arteries. Although
small, these arteries supply critical areas of the brain. The middle cerebral artery
continues laterally to dive into the lateral sulcus (Sylvian fissure) deep to the
Neuroscience Laboratory Manual 20
rostral pole of the temporal lobe. Branches of the middle cerebral artery can be
seen on the lateral surface of the brain as they emerge from the lateral sulcus.
On the ventral surface of the whole brain, the anterior cerebral arteries can be seen
coursing medially to pass dorsal (deep) to the optic nerves. As they approach the
midline just rostral to the optic chiasm, these arteries are joined together by an
anastomotic channel called the anterior communicating artery. Both anterior
cerebral arteries then disappear by diving into the interhemispheric fissure, each
one supplying ipsilateral structures on the medial and dorsal surface of the brain.
On your half brains, follow the course of an anterior cerebral artery as it courses
along the rostral and dorsal surfaces of the genu of the corpus callosum. At this
point, the anterior cerebral artery typically divides into its two terminal branches,
the pericallosal and callosomarginal arteries. The pericallosal artery runs caudally
along the dorsal surface of the body of the corpus callosum. The callosomarginal
artery takes a more dorsal path caudally by running in or near the cingulate sulcus.
Note the branches of these arteries and the general areas they supply.
Now turn your attention back to the ventral surface of the whole brain. The
posterior cerebrals, posterior communicating, internal carotids, anterior
cerebrals and anterior communicating arteries form an arterial circle (of Willis) at
the base of the brain surrounding the hypothalamus, infundibulum and optic
chiasm. You may be able to see many small arteries arising from the internal
surfaces of the circle of Willis. They are generally referred to as central or
ganglionic arteries. The circle of Willis is clinically important in that if a blood vessel
should be occluded on one side of the circle, blood can be shunted to bypass the
obstruction. However, since this arterial circle is variable (i.e., branches small or
missing), this is not an iron-clad rule.
Another issue to consider is that although there is some overlap along the
periphery of the territory for adjacent arteries supplying the brain, these arteries
are functionally "end" arteries, in that they are the sole blood supply to the vast
majority of a given area of brain. Consequently, permanent or prolonged occlusion
of a single artery results in necrosis of the brain area supplied by that artery.
Neuroscience Laboratory Manual 21
Venous Return -- Unlike the arterial supply to the brain, venules emerge from the
substance of the brain as fine pial plexuses that coalesce to form larger visible veins
that reside in the subarachnoid space. A good example of this can be seen on the
surface of the cerebral hemispheres. An exception to this general rule can be seen
on the medial surface of a half brain. Look along the dorsomedial aspect of the
thalamus on a half brain. A relatively large vein can usually be seen running in a
rostrocaudal direction. This vein drains deeper brain structures and is called the
internal cerebral vein. As this vein reaches the subarachnoid space at the caudal
aspect of the thalamus, you may be able to see another vein joining the internal
cerebral vein from the ventral side. This is the basal vein (of Rosenthal). If you do
not have this vein on your specimen, it can be seen on demonstration. After it is
joined by the basal vein, the internal cerebral vein becomes the great cerebral vein
(of Galen). NOTE: the paired (i.e., left and right) internal cerebral and basal veins
are tributaries of the single great cerebral vein. Into what venous structure does
the great cerebral vein empty? What is the name of the subarachnoid compartment
where the above veins join together?
Although the larger veins within the subarachnoid space on the surface of the brain
generally run in parallel with their arterial counterparts, these veins soon depart
from the arteries to drain into specialized endothelium-lined venous channels
between the meningeal and periosteal layers of the dura mater called dural venous
sinuses. These sinuses are formed in certain regions of the cranial cavity where the
inner (meningeal) layer of dura mater separates from the outer (periosteal) layer
to form: 1) horizontal septae that divide the cranial cavity into compartments, or
2) vertical septae that occupy the fissures between the left and right cerebral and
cerebellar hemispheres.
Using any gross anatomy text or atlas, identify and note the location of the
following dural septae and major dural venous sinuses: falx cerebri, superior
sagittal sinus, inferior sagittal sinus, tentorium cerebelli, tentorial notch
(incisure), straight sinus, confluence of sinuses, transverse sinus, sigmoid sinus
and cavernous sinus. What subdivision of the brainstem occupies the region within
the tentorial notch? At this time, you should review the direction of normal blood
flow in these dural venous sinuses. What major vein receives blood from the
sigmoid sinus?
Neuroscience Laboratory Manual 22
Spinal Cord -- The spinal cord has a longitudinal and segmental blood supply. The
longitudinal supply is provided by the single anterior and, if present, paired
posterior spinal arteries arising from the vertebral arteries. However, these small
arteries alone are only sufficient to supply upper cervical segments. Consequently,
the primary source of spinal cord blood supply is provided by segmental arteries at
cervical, thoracic and upper lumbar levels of the vertebral column. These arteries
gain access to the spinal cord through intervertebral foramina where they reinforce
the longitudinal supply through anastomotic channels.
ANIMATION
Brain arterial systems
DEMONSTRATIONS
Skull showing dural reflections and venous sinuses: falx cerebri, superior
sagittal sinus, inferior sagittal sinus, tentorium cerebelli, tentorial notch
(incisure), straight sinus, confluence of sinuses, transverse sinus.
Ventral surface of whole brain showing blood supply: Identify blood vessels
as labeled in Fig. 4 (p. 18) of this laboratory exercise.
Neuroscience Laboratory Manual 23
CSF AND VENTRICLES OF THE BRAIN
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Identify and locate all parts of the ventricular system of the brain.
2. Identify the brain structures that form the walls/boundaries of the various parts of the ventricular system.
3. Trace the normal flow of CSF through the ventricles and the general consequences of ventricular system blockage.
___________________________________________________________________
The brain is not a solid mass of nervous tissue. There are four interconnected
cavities, called ventricles, deep within the brain. The two lateral ventricles are
located within the cerebral hemispheres. The third ventricle is situated in the
midline between the left and right portions of the thalamus and hypothalamus.
The fourth ventricle is located between the cerebellum dorsally, and the pons and
medulla ventrally. Each ventricle contains structures called choroid plexuses,
which produce cerebrospinal fluid (CSF). The normal flow of CSF within the
ventricular system is as follows: lateral → third → fourth. After it flows through
the ventricles, it then gains access to the subarachnoid space through small
foramina in the fourth ventricle. The CSF then percolates throughout the
subarachnoid space surrounding the brain and spinal cord to eventually empty into
the venous system. In addition to supporting and protecting the brain, CSF is
important in the metabolic processes of the brain. The CSF also serves as an
important diagnostic tool for a variety of neurological problems, and can be
aspirated for analysis. It is critical that the CSF has unobstructed flow through the
ventricular system of the brain and into the subarachnoid space. If blockage should
occur, there will be a subsequent expansion of "upstream" ventricles
(hydrocephalus), causing compression of surrounding brain tissue.
Half Brain; Horizontal and Coronal Sections
Observe the medial surface of your half brain specimen. Find the thalamus and
hypothalamus. The area between (medial to) these structures and their
Neuroscience Laboratory Manual 24
contralateral counterparts is the third ventricle. Find the anterior commissure and
the rostral pole of the thalamus. Between these structures is a small hole called
the interventricular foramen (of Monro). There are two of these foramina, one on
each side. They interconnect the lateral ventricles with the third ventricle. If
present, the choroid plexus can be seen hanging from the roof of the third
ventricle. At the caudal end of the thalamus, the third ventricle narrows into a
small passageway, the cerebral aqueduct (of Sylvius), which courses through the
midbrain to open into the fourth ventricle. The fourth ventricle is continuous
caudally with the central canal of the spinal cord. Attempt to find the choroid
plexus in the fourth ventricle. It is from the fourth ventricle that the CSF enters the
subarachnoid space. It does so by passing through: 1) a single midline foramen
(foramen of Magendie) located at the caudal extent of the fourth ventricle where
the inferior medullary velum contacts the medulla, and 2) two lateral foramina
(foramina of Luschka) located at the lateral extremes of the fourth ventricle. The
foramina of Luschka can be found by GENTLY insinuating the tip of your blunt probe
into the lateral reaches of the fourth ventricle. If you have done this correctly, the
tip of the probe will pass through the foramen of Luschka to appear externally in
the cerebellopontine angle. It is common for the choroid plexus of the fourth
ventricle to extend through the foramina of Luschka to reside in the subarachnoid
space. Look in the region of the cerebellopontine angle for tufts of this structure
as it emerges.
The lateral ventricles are located in the cerebral hemispheres. They can be viewed
in their entirety by using both horizontal and coronal brain slices. Using your brain
atlas, begin at the dorsal aspect of the horizontally sliced brain and remove slices,
observing both surfaces of each slice, until the lateral ventricles are exposed. Note
that the fibers of the corpus callosum form the roof, as well as the anterior and
posterior boundaries of the lateral ventricles. Identify the genu, body and
splenium of the corpus callosum. Find the choroid plexus within the lumen of the
lateral ventricles and third ventricle. Identify the frontal (anterior) horn, body and
occipital (posterior) horn of the lateral ventricles. Note the rounded mass that
forms the lateral boundary of the frontal horns. This is the head of the caudate
nucleus, a component of the basal ganglia. Find the thalamus, septum pellucidum
and fornix, and determine their spatial relationships to the lateral ventricles. As
you progress from dorsal to ventral, there is a region near the caudal end of the
Neuroscience Laboratory Manual 25
lateral ventricles where the body, occipital horn and temporal (inferior) horn
meet. This is called the trigone (atrium) of the lateral ventricle. Follow subsequent
sections ventrally into the temporal horn.
Find a horizontal section similar to that in the Fix Atlas: Plate 56 (p. 112) and identify
the interventricular foramina (of Monro). As previously stated, these two
foramina are the openings from the lateral ventricles into the centrally located
third ventricle. Just lateral to each of these foramina is a "V" shaped region of white
matter called the internal capsule, an important bidirectional pathway between
the cortex and the brainstem and spinal cord. The apex of each "V" is called the
genu of the internal capsule. Each genu is directed medially and points at the
interventricular foramen on each side, thus serving as a landmark. The genu is
continuous with the anterior and posterior limbs of the internal capsule.
Using your coronal brain slices and your brain atlas, identify the same structures
you found in the horizontal sections. Compare and contrast these structures as
they appear in horizontal and coronal section. The purpose of this important
exercise is to begin to appreciate and understand the three dimensional anatomy
of the brain, which is critical if you are to be successful in this block.
NEURORADIOLOGY
You should now have a basic understanding of the gross anatomy of the brain. If
this assumption is correct, you should have little difficulty transferring this
knowledge to interpret the variety of radiologic techniques that are used to
visualize the various parts of the brain.
Using your Neuroscience slide set, look at slide 45. This is a mid-sagittal section of
the brain as visualized by magnetic resonance imaging (MRI). This particular MRI is
a T1 weighted image. What are the visual characteristics of a T1 weighted MRI of
the brain such as the one seen on this slide? Identify the following brain
structures/regions on this slide with the help of your half brain specimens: corpus
callosum (all portions), cingulate gyrus, fornix, thalamus, cerebral aqueduct (note
arrowheads), subarachnoid cisterns (interpeduncular, pontine, superior
cerebellar, cisterna magna), parietooccipital sulcus, calcarine fissure, cuneus,
lingula, cerebellum, fourth ventricle, medulla, pons, midbrain, superior and
Neuroscience Laboratory Manual 26
inferior colliculi, mammillary body, hypothalamus, optic chiasm, optic nerve and
interventricular foramen of Monro.
Slide 46 is an MRI (T1 weighted) of the brain in coronal section. Using a similar
coronal slice from your brain specimens as an aid, identify the lateral ventricles,
third ventricle, thalamus, body of the corpus callosum, lateral fissure, insula,
temporal lobe and interhemispheric fissure.
Slide 47 is a T1 weighted MRI taken in the horizontal plane. Using a similar
horizontal slice from your brain specimens as an aid, identify the frontal horns of
the lateral ventricles, third ventricle, head of the caudate, thalamus, internal
capsule (all parts), trigone (atrium) of lateral ventricle, splenium of corpus
callosum, lateral fissure and insula.
Slide 51 shows two T2 weighted horizontal images of the brain. In the left image,
note the occipital horn of the lateral ventricle on the left side of the slide. Is this
the patient’s left side? Which of the two images is higher (more superior)? The
midbrain and the middle and posterior cerebral arteries can also be seen. Note
the location and orientation of the cerebral peduncles. Verify this by comparing
this image with a similar horizontal section from your brain specimens. The right
image shows the frontal horns of the lateral ventricles, third ventricle, and trigone
(atrium) of the lateral ventricles. How does the appearance of the ventricles on
this slide differ from that seen in a T1 weighted image? Slide 65 is a similar MRI,
showing anterior, middle and posterior cerebral arteries as well as mammillary
bodies, third ventricle, rostral midbrain and uncus. Is this a T1 or T2 weighted
image? Look at slide 64. Is this section rostral or caudal to slide 65? What blood
vessels can be seen in this view?
ANIMATIONS
Ventricles (midline)
Ventricles (trans)
Ventricles (X, X2, Y)
DEMONSTRATIONS
Cast of human ventricular
system.
Neuroscience Laboratory Manual 27
INTRODUCTION TO THE MACROSCOPIC ANATOMY OF THE NEURAXIS
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Be able to quickly identify representative levels of the neuraxis, including the salient internal and external features of these representative levels as viewed on the stained, macroscopic sections in your slide sets.
2. Attempt to discern the plane-of-section of each of the slides (horizontal, coronal, sagittal, etc.).
3. Distinguish cytological staining differences between collections of cell bodies (i.e., nuclei and/or ganglia) versus nerve fibers/tracts.
___________________________________________________________________
As part of the learning aids in the neuroscience laboratory, you have been provided
with a set of slides showing the macroscopic anatomy of the human brain and
spinal cord. The slides are arranged in ascending order, beginning with the sacral
spinal cord (slide #1) and ending with telencephalic structures. Those sections of
the neuraxis from spinal cord through midbrain are cut in horizontal section.
Because of the flexure of the brain between the diencephalon and midbrain,
subsequent slides show brain sections cut in varying planes between horizontal and
coronal. The purpose of the following exercise is to familiarize you with the
"typical" appearance of the various levels of the spinal cord and brainstem so that
you can instantly recognize these levels when you see them. Make extensive use
of your Fix brain atlas, and the supplementary labeled slides (available on eCampus
and at the back of this laboratory syllabus), to assist you in the identification of
internal and external landmarks at these various levels.
Spinal Cord (slides 1-5)
Observe slide 1. This is a cross section of the sacral spinal cord. The dorsal surface
of this section, as well as subsequent sections of spinal cord and brainstem through
the midbrain, is located at the top of the slide. The vast majority of the sections on
Neuroscience Laboratory Manual 28
the slides are stained with one of two types of nerve fiber stains. Slide 1 is stained
by the luxol fast blue method for myelinated nerve fibers, and counterstained with
hematoxylin and eosin to reveal neuronal cell bodies. Note the dark blue staining
of the white matter (nerve fibers) around the periphery, and the relative absence
of blue staining in the centrally located gray matter, which contains neuronal cell
bodies. The butterfly shaped gray matter is divided into dorsal (posterior) and
ventral (anterior) horns with an intervening lateral horn. The latter will be seen
more clearly in subsequent sections. Note the gray commissure that connects the
left and right sides of the gray matter. Observe the small purple dots scattered
throughout the ventral horn. These are the ventral motor horn cells that give rise
to the majority of axons within the ventral roots. Observe the arched pink region
near the top of the dorsal horn. This is the substantia gelatinosa, an important
sensory relay nucleus. The gray matter immediately ventral to the substantia
gelatinosa contains the less distinct nucleus proprius (proper sensory nucleus).
The white matter dorsal to the substantia gelatinosa is Lissaur's tract, an
intersegmental spinal pathway. The white matter can be roughly divided into
funiculi (columns) based on their position in the spinal cord. The dorsal funiculus
is located between the dorsal horns of the gray matter. The lateral funiculus
occupies the region between the dorsal and ventral roots. The ventral funiculus
lies between the midline and the emergence of the ventral roots. Immediately
ventral to the gray commissure is the anterior white commissure, which contains
nerve fibers that cross the midline. The prominent dorsal and ventral median
fissures serve to vertically divide the white matter at the midline. Each of the above
funiculi contain important ascending and descending nerve fiber tracts that will be
identified at a later date. Note the single anterior spinal artery and the multiple
posterior spinal arteries and their location immediately external to the pia mater.
Now look at slide 2. This is a cross section of the lower lumbar spinal cord stained
with the Weil stain. This histological procedure stains the myelin of nerve fibers
black. The gray matter (cell bodies) remains unstained with the exception of those
regions where myelinated nerve fibers traverse it. Observe the large lateral
projections of the ventral horns. What is the purpose of these lateral extensions?
Why would you expect to see them at this spinal level? In slide 2, and all
subsequent slides of the spinal cord (slides 3-5), identify all of the structures you
found on slide 1.
Neuroscience Laboratory Manual 29
Slide 3 (upper lumbar) appears similar to slide 2. Dentate (denticulate) ligaments
can be clearly seen in this section. What tissue layer comprises the dentate
ligaments? What are their functions?
Slide 4 (thoracic) reveals the prominent intermediolateral gray (cell) column.
What specific cell type is contained within this column? Why is the gray matter so
small in the thoracic region?
Slide 5 is at the C-1 spinal level. Although it resembles the thoracic spinal cord,
there are some distinct differences. The intermediolateral cell column has been
replaced by the spinal accessory nucleus. How would the gray matter differ if this
were a lower cervical section? In addition, at this level the substantia gelatinosa is
replaced by the spinal nucleus of V (spinal trigeminal nucleus). A roughly circular
region of white matter in the lateral funiculus near the base of the dorsal horn is
separated into multiple fascicles. This is the lateral corticospinal tract, an
important descending pathway which has just decussated (crossed the midline) at
more rostral levels to assume its position within the lateral funiculus.
Compare the relative appearances of the spinal cord in slides 1 (sacral), 2 (lower
lumbar), 3 (upper lumbar), 4 (thoracic), 5 (cervical) and be able to recognize and
identify each level by listing their major differences.
Medulla (slides 7,12)
Slide 7 is a representative section of the caudal medulla. This level is occasionally
referred to as the "closed" portion of the medulla, since it is caudal to the fourth
ventricle and thus reveals a "closed" central canal surrounded by nuclei and fiber
tracts. The prominent spinal nucleus of V can be seen. The dorsal column region
now displays a nucleus (nucleus gracilis) on either side of the midline. What
external feature reveals the location of these nuclei? The thick, black "X" at the
midline ventrally is the decussation of the pyramids, a crossing of descending
nerve fibers that will form the previously mentioned lateral corticospinal tracts
seen in slide 5.
Slide 12 is a typical representation of the rostral medulla. This level is also called
the "open" medulla because the central canal has "opened" to form the floor of the
Neuroscience Laboratory Manual 30
fourth ventricle. This level is immediately recognizable by the pyramids ventrally,
the coiled appearance of the inferior olivary nuclei, the well-defined inferior
cerebellar peduncles, fourth ventricle and overlying cerebellum. The medial
lemniscus, an important ascending sensory pathway, can be seen in the midline
sandwiched between the left and right inferior olivary nuclei. Also note the choroid
plexus within the fourth ventricle and its extension through the foramina of
Luschka to lie externally within the cerebellopontine angle. The inferior olivary
nuclei cause an external bulge, the inferior olive. Immediately ventral and dorsal
to the inferior olive are the pre- and post-olivary sulci, respectively. What cranial
nerves emerge from each of these sulci?
Pons (slides 16,17,19)
Slide 17 is a cross section of the caudal 1/3 of the pons. The characteristic ventral
convexity of the ventral pons can be clearly seen. Imbedded within this region are
the dark stained fascicles comprising the pyramidal tracts, which are surrounded
by the intervening light areas which are the pontine nuclei. Dorsal to the pyramidal
tracts is the medial lemniscus. At this level, it is shaped like a handlebar mustache
and forms the dorsal border of the ventral pons. It is located in a region of the pons
called the pontine tegmentum, which extends dorsally to form the floor of the
fourth ventricle. The large black areas forming the lateral boundaries of the pons
at this level are the middle cerebellar peduncles (brachium pontis). In the pontine
tegmentum just medial to the middle cerebellar peduncles, the fascicles of the
facial nerve (CN VII) can be seen as they traverse the pons to emerge caudally at
the cerebellopontine angle. Identify the above pontine structures on slide 16,
where the superior, inferior and middle cerebellar peduncles can be seen
simultaneously. Can you find the emerging fibers of the abducens nerve (CN VI) in
this section? Compare these sections with slide 19 (rostral pons) where you should
be able to identify the superior cerebellar peduncles, fourth ventricle, ventral
pons, pyramidal tracts, and medial lemniscus.
Midbrain (slides 21,23)
All levels of the midbrain are characterized by the cerebral peduncles (crus cerebri)
and interpeduncular fossa ventrally, the substantia nigra (the clear region
Neuroscience Laboratory Manual 31
immediately dorsal to the crus cerebri) and the medial lemniscus (dorsomedial to
the substantia nigra).
The level of the inferior colliculus (slide 21) has unique characteristics, which
include the decussation of the superior cerebellar peduncles, the nucleus of CN IV
and the distinct nuclei of the inferior colliculi.
The level of the superior colliculus (slide 23) is characterized by the paired red
nuclei, nuclear complex of the oculomotor nerve (CN III) and the emerging
rootlets of CN III as they pass through the red nuclei to emerge from the midbrain
along the walls of the interpeduncular fossa.
Diencephalon (slides 23,29)
In addition to midbrain, slide 23 also contains some of the caudal structures of the
thalamus, a major subdivision of the diencephalon. These structures of the
thalamus are the pulvinar and the medial and lateral geniculate bodies. Slide 29
reveals more of the nuclei of the thalamus, including two important sensory relay
nuclei, the ventral posteromedial (VPM) and ventral posterolateral (VPL) nuclei,
as well as the pulvinar. The mammillary bodies are also clearly seen. Midbrain
structures such as the cerebral peduncles, substantia nigra and red nuclei are also
present. Notice how the cerebral peduncles merge with the posterior limb of the
internal capsule. Using your half brains, figure out the plane of section of slide 29.
NEURORADIOLOGY
Slide 52 is a midsagittal MRI through the cervical region. Identify the spinal cord,
vertebral bodies and intervertebral disks. Note the abnormality in the spinal cord
at C3-4 (herniated disk).
Slide 53 is a midsagittal MRI through the lumbar and upper sacral region. Find the
subarachnoid space, intervertebral disks and termination of the spinal cord. Is
this a T1 or T2 weighted image? Using your anatomical knowledge from Gross
Anatomy, can you identify, by number, the location of the bodies of the lumbar
vertebrae?
Neuroscience Laboratory Manual 32
Slides 58-65 are axial (cross section) MRI’s of the cervical spinal cord (slide 58)
through the rostral midbrain (slide 65). All of these sections are T2 weighted. Make
note that the orientation of the neuraxis on these radiographic slides is opposite to
what you saw on the stained sections (i.e., the dorsal aspect of each scan is toward
the bottom of the slide). On slide 58, note the characteristic dorsoventral
flattening of the cervical spinal cord and the vertebral arteries located in the
foramina transversaria. On slide 59 (caudal medulla), note the vertebral arteries,
pyramids and central canal. Slide 60 (rostral medulla) clearly shows the inferior
cerebellar peduncles, inferior olive and pyramids as well as the joining of the two
vertebral arteries to form the basilar artery. At this level, the central canal has
opened up into the 4th ventricle. Slide 61 (transition from rostral medulla to caudal
pons) shows the 4th ventricle, middle cerebellar peduncles, CN’s VI, VII & VIII and
the basilar artery. Slide 62 (midpons) shows the middle cerebellar peduncle, CN
V as it emerges from the middle cerebellar peduncle, 4th ventricle and the basilar
artery. Slide 63 (rostral pons) shows the characteristic shape of the ventral pons,
as well as the rostral extent of the 4th ventricle, both middle and superior
cerebellar peduncles and the basilar artery. Slide 64 (caudal midbrain) shows the
characteristic outline of the midbrain, including the cerebral peduncles,
interpeduncular fossa and inferior colliculus. At this level, the superior cerebellar
arteries can be seen arising from the basilar artery to embrace the midbrain. The
internal carotid arteries, uncus and temporal horn of the lateral ventricles can
also be seen in this slide. Slide 65 (rostral midbrain) shows a number of structures
including cerebral peduncles, interpeduncular fossa, superior colliculi, red nuclei,
mammillary bodies, hypothalamus, uncus and third ventricle. In addition, the
posterior cerebral, middle cerebral, anterior cerebral and internal carotid arteries
can be seen as well as the superior cerebellar cistern. To verify what you are seeing
on slide 65, compare it to a similar horizontal wet brain section.
ANIMATIONS
Coronal MRI
Horizontal MRI
Neuroscience Laboratory Manual 33
ASCENDING SENSORY PATHWAYS
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the location and function of each of the described pathways at all levels of the neuraxis, from their origin to their termination in the cerebral cortex.
2. Be able to determine the clinical signs and symptoms resulting from lesions of these pathways at any level of the neuraxis.
3. Trace the two primary ascending sensory pathways from the body and posterior 1/3 of the head and the specific sensory information (modalities) these pathways convey.
4. Demonstrate the somatotopic organization of ascending sensory pathways and how fibers are organized in each pathway. Describe the sensory homunculus of the primary somatosensory cortex.
___________________________________________________________________
There are a number of ascending pathways in the neuraxis that carry a variety of
different types (modalities) of sensory information from the body, extremities and
head to the cerebral cortex. Those dealing with the body, extremities and posterior
1/3 of the head receive their input from the dorsal roots of spinal nerves. Those
pathways transmitting sensory information to the cortex from the anterior 2/3 of
the head (e.g., face, nasal cavities, oral cavity, pharynx, larynx, etc.) receive their
input from the cranial nerves. We will concentrate our efforts on those pathways
that are clinically relevant and produce consistent, repeatable sensory deficits
when lesioned (injured). In studying these pathways, it is best to follow each one
from its origins in the spinal cord to its thalamic terminations using the slide set.
Ascending sensory pathways from the body and posterior 1/3 of the head -- The
first order (1o) neurons (the first neuron in the pathway) for all sensory pathways
from the body and posterior 1/3 of the head reside in the dorsal root ganglia of the
spinal nerves. The central processes of these cells enter the spinal cord via the
dorsal roots to either synapse in the spinal cord and/or ascend to brainstem levels.
Neuroscience Laboratory Manual 34
The nerve fibers in these sensory pathways are typically arranged in a somatotopic
(i.e., maintaining an organized relationship to a specific part of the body) fashion
throughout their ascent through the spinal cord, brainstem and telencephalon.
1. Anterolateral System (Spinal Lemniscus)
a. Lateral spinothalamic tract [Modalities: pain and temperature]
b. Anterior (ventral) spinothalamic tract [Modalities: crude (light) touch]
c. Spinotectal tract [Modality: pain]. This pathway is the afferent limb of a
“reflex” pathway that results in reflexive turning of the head and eyes in
response to a painful (nociceptive) stimulus.
These pathways will be studied together since they occupy similar positions within
the neuraxis. They are listed above in descending order of their relative clinical
importance. The lateral spinothalamic tract is, by far, the most important
pathway. The cell bodies of first order neurons for these pathways lie in the dorsal
root ganglia in all spinal nerves (except C-1). The central processes of these cells
terminate in the dorsal horn in either the substantia gelatinosa or the nucleus
proprius. Second order (2o) neurons in these nuclei give rise to axons that cross
the midline in the anterior white commissure to assume a peripheral position in
the ventral aspect of the contralateral lateral funiculus as the lateral spinothalamic
tract (and spinotectal tract), or a slightly more ventral position (anterior
spinothalamic tract) (slide 1, slide 2, slide 3, slide 4, and slide 5). As these fibers
cross the midline, they ascend 1-3 spinal segments before they join their respective
contralateral fiber tracts. How would this bit of knowledge affect the level of
sensory deficits if a lesion of the lateral spinothalamic tract occurred at the T-10
spinal level?
These three pathways ascend together throughout the spinal cord and brainstem,
and are often referred to collectively as the spinal lemniscus or anterolateral
system. When they enter the medulla, they can be found in the lateral aspect just
dorsal to the inferior olivary nucleus (slide 9, slide 12, slide 14 and slide 15). In the
pons and midbrain (slide 16, slide 17, slide 18, slide 19, slide 20, slide 21, slide 22,
slide 23 and slide 24) the spinal lemniscus can be found lateral to the medial
lemniscus. The remaining lateral and anterior spinothalamic tracts continue
Neuroscience Laboratory Manual 35
rostrally to terminate in the ipsilateral ventral posterolateral (VPL) nucleus of the
thalamus, where third order (3o) neurons in the VPL then project their axons to the
postcentral gyrus via the posterior limb of the internal capsule (slide 29, slide 30
and slide 31) and corona radiata.
2. The Dorsal Column / Medial Lemniscus Pathway [Modalities: fine tactile (touch
& pressure), vibration, proprioception/kinesthesia (position/movement sense)]
This ascending pathway is anatomically and functionally separated into two distinct
pathways within the dorsal columns of the spinal cord. Central processes from
dorsal root ganglia (1o neurons) gain access to the spinal cord and ascend in the
ipsilateral dorsal column without synapsing in the spinal cord. Information coming
into the spinal cord from the lower extremities up to approximately the T-7 spinal
level, form a single ipsilateral pathway in the dorsal columns called the fasciculus
gracilis (slide 1, slide 2, slide 3 and slide 4). The central processes for dorsal root
ganglion cells from T-6 up through C-2 (C-1 spinal nerves have no dorsal root
ganglia) ascends in the dorsal columns lateral to the fasciculus gracilis as the
fasciculus cuneatus (slide 5 and slide 6). As these pathways ascend into the
medulla, they remain in their same relative positions (slide 6). The fasciculus
gracilis terminates in the nucleus gracilis, which appears at more caudal levels,
while the fasciculus cuneatus continues to ascend to more rostral levels of the
medulla to terminate in the nucleus cuneatus (slide 7 and slide 8).
Second order (2o) neurons in the nucleus gracilis and nucleus cuneatus give rise to
axons that sweep ventrally as the internal arcuate fibers to cross the midline
(sensory decussation/decussation of the medial lemniscus) and form the
contralateral ascending fiber bundle called the medial lemniscus (slide 8). These
axons then ascend somatotopically within the medial lemniscus through the
medulla (slide 9, slide 10, slide 12, slide 13 and slide 14), pons (slide 16, slide 17,
slide 18, slide 19 and slide 20) and midbrain (slide 21, slide 22, slide 23, slide 24
and slide 26) to terminate on third order (3o) neurons located in the ipsilateral
ventral posterolateral (VPL) nucleus of the thalamus (slide 29).
Third order (3o) neurons in the VPL give rise to axons that gain access to the
posterior limb of the internal capsule (slide 29, slide 30 and slide 31). These axons
Neuroscience Laboratory Manual 36
then fan out in the corona radiata to terminate primarily in the postcentral gyrus
(Brodmann's areas 3,1,2). DEMONSTRATIONS
Posterior Limb of the Internal Capsule
Postcentral Gyrus (Brodmann’s areas 3,1,2)
Neuroscience Laboratory Manual 37
SENSORY PATHWAYS FOR THE ANTERIOR 2/3 OF THE HEAD
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the location and function of each of the described pathways at all levels of the neuraxis, from their origin to their termination in the cerebral cortex.
2. Be able to determine the clinical signs and symptoms resulting from lesions of these pathways at any level of the neuraxis.
3. List the four cranial nerves conveying sensation from the anterior 2/3 of the head.
4. Trace the ascending sensory pathways from the anterior 2/3 of the head and the specific sensory information (modalities) these pathways convey.
5. Discuss how the proprioceptive pathway from the anterior 2/3 of the head differs from pain, temperature, pressure and vibration pathways.
6. Demonstrate the somatotopic organization of ascending sensory pathways and how fibers are organized in each pathway. Describe the sensory homunculus of the primary somatosensory cortex.
___________________________________________________________________
The vast majority of sensation from the external surface of the anterior 2/3 of the
head is provided by the trigeminal nerve (CN V) by way of its three divisions
(ophthalmic, maxillary and mandibular) with the remainder being supplied by CN
VII, IX and X. With the exception of proprioception and possibly pressure, the 1o
neurons in each of the following pathways are located in the sensory ganglia
associated with each of the above cranial nerves. For the modalities of pain and
temperature, the central processes from each of these sensory ganglia have the
same central pathways.
1. Pain and Temperature -- On your whole brain specimens, find CN V and VII, and
make careful note of where they emerge from the brainstem. Now observe slide
16 and slide 17. These are cross sections through the caudal pons. On both slides,
Neuroscience Laboratory Manual 38
note the facial colliculus forming the floor of the fourth ventricle, and the fascicles
of CN VII as they arch through the pontine tegmentum to exit the brainstem
ventrally. Just lateral to the axons of CN VII in the pontine tegmentum is a relatively
clear, oval area, the spinal nucleus of V. Surrounding the spinal nucleus of V on the
lateral side is a kidney-shaped area of nerve fibers, the descending (spinal) tract of
V. Both the spinal tract and nucleus of V are present from this point (i.e., caudal
pons) caudally to the level of the upper cervical spinal cord, where they are
replaced by Lissaur's tract and the substantia gelatinosa, respectively. Verify this
by following the spinal tract and nucleus of V caudally (slide 17, slide 16, slide 15,
slide 14, slide 13, slide 12, slide 10, slide 9, slide 8, slide 7, slide 6 and slide 5). 2o
neurons in the spinal nucleus of V give rise to axons that cross the midline obliquely
and ascend as the ventral trigeminothalamic tract (trigeminal lemniscus). (NOTE:
There is still some uncertainty as to the exact location of this tract in humans so we
will not require you to know the location of the trigeminal lemniscus in the
medulla). As the medial lemniscus flattens dorsoventrally in the pons (slide 16,
slide 18, and slide 19), the trigeminal lemniscus remains on its dorsal aspect,
sandwiched between the medial lemniscus and the overlying central tegmental
tract.
In the midbrain, the trigeminal lemniscus assumes a position along the medial
concave surface of the medial lemniscus as the latter fans out laterally and dorsally
(slide 20, slide 21, and slide 23) to assume a more vertical orientation. The
ascending 2o axons in the trigeminal lemniscus terminate in the ventral
posteromedial nucleus (VPM) of the thalamus (slide 29). 3o neurons in the VPM
give rise to axons that travel through the posterior limb of the internal capsule
(slide 29, slide 30 and slide 31) and through the corona radiata (see demonstration)
to terminate in the postcentral gyrus near the Sylvian fissure.
2. Fine Touch, Vibration and Pressure -- The central processes of the trigeminal
ganglion cells course into the mid pons via CN V and terminate ipsilaterally on the
enlarged rostral extension of the spinal nucleus of V, called the chief (principal)
sensory nucleus of V. This nucleus lies in the lateral-most aspect of the pontine
tegmentum just medial to the middle cerebellar peduncle (slide 18). The 2o
neurons in this nucleus give rise to axons that cross the midline obliquely and
ascend to join the trigeminal lemniscus at midbrain levels (slide 20, slide 21, and
Neuroscience Laboratory Manual 39
slide 23 ). These nerve fibers then follow the exact synaptic pathway to the cortex
as described above for pain and temperature fibers for the anterior 2/3rds of the
head. How would the symptoms differ in a lesion of the trigeminal lemniscus in the
caudal pons, as opposed to a lesion of this structure at the superior collicular level?
3. Proprioception [and pressure (?)] -- In the case of proprioception, and possibly
pressure, the 1o neurons in this pathway do not lie in the trigeminal ganglia, but
instead lie within the mesencephalic nucleus of V, which resides in the brainstem
from the mid pons to the superior collicular level of the midbrain. In the mid pons,
this nucleus is located dorsomedial to the chief sensory nucleus of V (slide 18). The
peripheral processes of these cells join CN V to be distributed with the three
divisions of this nerve. They accomplish this by forming a small, sickle shaped
fascicle of nerve fibers immediately ventrolateral to the mesencephalic nucleus of
V. These fibers are called the mesencephalic root (tract) of V (slide 18). In the
midbrain (slide 21 and slide 22), the mesencephalic nucleus of V can be seen as a
lateral outpocketing of the periaqueductal gray at the approximate level of the
floor of the cerebral aqueduct. The mesencephalic root of V can be seen as a thin
rim of fibers surrounding the lateral aspect of the nucleus. The central processes
of the mesencephalic nucleus of V project to the pontine and midbrain reticular
formation (RF), which eventually transmits proprioceptive information to the
cerebral cortex, either directly or through the thalamus.
ANIMATIONS
Somatosensory radiations
DEMONSTRATIONS
Internal Capsule
Postcentral Gyrus (Brodmann’s areas 3,1,2)
Neuroscience Laboratory Manual 40
THE PYRAMIDAL SYSTEM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the location and function of each of the described pathways at all levels of the neuraxis from their origin in the cerebral cortex to their termination in the brainstem and spinal cord.
2. Determine the clinical signs and symptoms resulting from lesions of these pathways at any level of the neuraxis in which they are located.
3. List which cranial nerve motor nuclei receive unilateral innervation from the corticobulbar tract.
4. Identify the specific brainstem level where the corticospinal tract decussates (crosses) to become the lateral corticospinal tract.
5. Distinguish the major clinical deficits following lesions of upper motor neurons (UMNs) vs. lower motor neurons (LMNs).
___________________________________________________________________
The term "pyramidal system" refers to the direct, volitional (voluntary) motor
pathways from the cerebral cortex to the motor nuclei that control the voluntary
muscles of the body, extremities and head. Conversely, the term "extrapyramidal
system" (to be studied later) refers to motor pathways from the cerebral cortex
that form loops with the basal ganglia and thalamus, and function in more
stereotypic movements and maintenance of posture.
Classically, the pyramidal system is subdivided into two parts: 1) the corticobulbar
tract, which terminates on cranial nerve motor nuclei within the brainstem and
thus controls the voluntary muscles of the head (and some in the neck) and; 2) the
corticospinal (pyramidal) tract, which provides descending nerve fibers from the
cortex to the motor cell columns in the spinal cord for voluntary movement of the
body and extremities.
Neuroscience Laboratory Manual 41
Whole and Half Brains; Horizontal and Coronal Sections
Although there are significant contributions from other areas of the cerebral cortex
(Brodmann's areas 6,8,1,2,5), both the corticobulbar and corticospinal tracts begin
primarily in the precentral gyrus (Brodmann's area 4). Find these regions on your
whole and/or half brains. The cortical neurons that reside in the above regions are
called upper motor neurons. These upper motor neurons are located
somatotopically within the precentral gyrus. The neurons for the corticobulbar
tract are located near the Sylvian fissure, whereas the neurons for the corticospinal
tract reside somatotopically in the remainder of the precentral gyrus as it arches
dorsally and medially. Study the motor homunculus on your lecture handout and
make sure you understand this concept. Axons arising from these upper motor
neurons descend through the corona radiata, which converges into the relatively
compact internal capsule (observe these structures on both your horizontal and
coronal sections). The corticobulbar fibers assume a compact position within the
genu of the internal capsule, which resides at the rostral pole of the thalamus. The
corticospinal axons reside in a compact, somatotopic fashion toward the caudal
extent of the posterior limb of the internal capsule. Can you think of a possible
negative consequence related to the compact nature of the corticobulbar and
corticospinal fibers as they descend through the internal capsule? As we descend
from diencephalic to midbrain levels, each internal capsule is continuous inferiorly
with the ipsilateral cerebral peduncle. Compare and contrast the appearance and
relationship of the internal capsule and cerebral peduncles on the horizontal and
coronal slices. This relationship can often be seen particularly well on your coronal
slices where the posterior limb of the internal capsule blends inferiorly with the
cerebral peduncles. Observing both coronal and horizontal slices, what structure
always resides immediately medial to the posterior limb of the internal capsule?
As the corticobulbar and corticospinal axons descend into the midbrain, they are
classically described as residing in the middle 3/5 of the cerebral peduncles, with
the corticobulbar fibers occupying the medial portion and the corticospinal fibers
arranged somatotopically with lower extremity fibers most lateral. The cerebral
peduncles can usually be seen cut in cross section on the most inferior horizontal
brain slice.
Neuroscience Laboratory Manual 42
Look on the ventral surface of your whole brain and note that the cerebral
peduncles terminate by disappearing caudally into the convexity of the ventral
pons. The pyramidal (corticospinal) tract emerges caudally in the medulla as the
pyramids. "What happened to the corticobulbar tract?", you may ask (Try to
figure this out before you read on). As the corticobulbar tract descends through the
midbrain and pons, nerve fibers from this tract are peeling off to synapse on the
motor nuclei of CN III, IV, V, VI and VII. The remaining fibers for the medullary
motor nuclei [nucleus ambiguus (motor nucleus for CN IX, X and XI) and the
hypoglossal nucleus] have also begun to separate from the corticospinal fibers in
the caudal pons to arch dorsally to synapse on these nuclei. Consequently, the vast
majority of the nerve fibers in the pyramids are those of the pyramidal
(corticospinal) tract. Find the longitudinal median fissure between the pyramids in
the rostral medulla. As you follow this distinct fissure caudally, it will blur, or fill in,
at the level of the caudal medulla. This is caused by the pyramidal decussation,
the crossing of the pyramidal tract to form the lateral corticospinal tract within the
spinal cord.
Slide Set (Don't put your brains away yet!)
Now, using your slide set and Fix atlas, follow the respective pathways of the
corticospinal and corticobulbar tracts. Begin with slide 35, which is a horizontal
section through the diencephalon at the level of the interventricular foramina of
Monro. The rostral direction is toward the top of the slide. Identify the anterior
limb, genu and posterior limb of the internal capsule. Also note the columns of
the fornix, third ventricle and thalamus. Now, find a slice from your horizontally
sectioned wet brain specimen that compares to slide 35 and find the same
structures as discussed above. Note, on both the slide and the brain slice, the
anatomical relationship between the posterior limb of the internal capsule and
the thalamus; this relationship serves to identify these structures in a variety of
planes.
View slide 32. This is roughly a coronal section through the mid thalamus. Find the
thalamus, posterior limb of the internal capsule, third ventricle and massa
intermedia. What is the space immediately dorsal to the massa intermedia? As
Neuroscience Laboratory Manual 43
you did previously, find a comparable coronal slice from your wet brain specimens
and compare it to this slide while you identify the above structures.
Slide 31, slide 30 and slide 29 show the transition between the posterior limb of
the internal capsule and the cerebral peduncles. Identify these structures, as well
as the thalamus and third ventricle.
Using slide 24, slide 23, and slide 21, follow and identify the corticospinal and
corticobulbar tracts caudally through the midbrain, noting the general location and
somatotopic arrangement of these tracts in the cerebral peduncles. On slide 20,
slide 19, slide 18, and slide 16, notice how these tracts are separated into loosely
arranged fascicles in the ventral pons. The fascicles of the corticobulbar tract are
represented in the dorsomedial region of these fascicles.
Slide 14, slide 13, slide 12, slide 10 and slide 9 show the typical, consistent
appearance and location of the pyramids from rostral to caudal medulla. Slide 8
illustrates the beginning of the pyramidal (motor) decussation. The median fissure
between the pyramids is displaced to the right at its apex and the dorsomedial
region of the right pyramid is beginning to move dorsally. The remaining
rostrocaudal extent of the pyramidal decussation is illustrated in slide 7 and slide
6, which demonstrate the fibers of the pyramidal tract crossing the midline to
assume a more dorsolateral location. Once these fibers attain their new position
contralaterally, they are called the lateral corticospinal tract. Slide 5 (spinal cord
level C-1) shows the location of the lateral corticospinal tracts as loose fascicles of
nerve fibers tucked into the concavity along the lateral surface of the dorsal and
ventral horns. The lateral corticospinal tract maintains this position throughout the
spinal cord (slide 4, slide 3, slide 2 and slide 1). Would the symptoms be the same
in an individual with a lesion of the right pyramid and another individual with a
lesion of the right lateral corticospinal tract? Can you explain and coherently defend
your answer?
DEMONSTRATIONS
Cerebral Peduncles
Pyramidal Decussation
Neuroscience Laboratory Manual 44
CRANIAL NERVES
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Locate and identify the cranial nerves on the wet brains and describe the various functions of each.
2. Describe the types of fibers (i.e., motor, sensory, autonomic, etc.) conveyed by each cranial nerves. Demonstrate a general understanding of “functional components.”
3. Determine the clinical signs and symptoms resulting from lesions involving all components of CN’s I, III, IV, V, VI, VII, IX, X, XI and XII.
4. Review the ascending sensory pathways and pyramidal system laboratories and list which sensory/motor nuclei are associated with specific cranial nerves.
___________________________________________________________________
There are twelve pairs of cranial nerves. A lesion to any one of these nerves results
in clinically demonstrable deficits. As such, any general neurological exam should
include an assessment of cranial nerve function. The purpose of this laboratory
session is to: 1) (re)acquaint you with the gross anatomy of the cranial nerves; 2)
illustrate the internal macroscopic anatomy of selected cranial nerves (CN I, III, IV,
V, VI, VII, IX, X, XI and XII); and 3) describe the distinctive functional components
(i.e., sensory, motor, autonomic, etc.) found within a given cranial nerve. The
remaining cranial nerves (CN II and VIII) will be studied, in detail, in subsequent
laboratory sessions.
Whole and Half Brains
Using your whole and half brains, turn them over to view the ventral surface and
observe the following:
CN I (olfactory nerve) -- This nerve provides us with our sense of smell. In addition
to its unique sensory function, the primary olfactory pathway is also unique among
the sensory pathways in that it does not have a relay through the thalamus to the
Neuroscience Laboratory Manual 45
cerebral cortex, but instead sends projections directly to phylogenetically older
cortical areas (paleocortex). Another unique aspect of the olfactory pathway is the
lack of a decussation (i.e., the pathway is ipsilateral). The 1o cell bodies in this
pathway are located in the upper reaches of the nasal cavity. The actual filaments
(axons) of CN I extend through the cribriform plate of the ethmoid bone as the
olfactory nerves, which project to neurons in the olfactory bulbs.
On the ventral surface of the brain, the olfactory bulbs can be seen on the surface
of the frontal lobes near the midline. As the olfactory tract (stalk) extends caudally
from the olfactory bulb, it divides into medial and lateral olfactory stria. The medial
olfactory stria crosses the midline via the anterior commissure to supply
interconnections between the left and right olfactory bulbs. The lateral olfactory
stria is the principal central projection pathway for the olfactory system that
extends toward the region of the uncus, where it synapses in the primary olfactory
cortex (periamygdaloid cortex, piriform cortex) and the amygdala.
CN II (optic nerve) -- The optic nerves mediate vision and are seen in the midline
just caudal to the olfactory tracts. The left and right optic nerves meet at the
midline and fuse, forming the optic chiasm. Two diverging nerve bundles, the optic
tracts, can be seen arching laterally and posteriorly from the optic chiasm to
interconnect with the diencephalon and midbrain.
CN III (oculomotor nerve) -- This nerve supplies motor innervation to the
extraocular muscles with the exception of the superior oblique and lateral rectus
muscles. In addition, it provides preganglionic parasympathetic fibers to the ciliary
ganglion, which, in turn, provides postganglionic parasympathetic innervation to
the sphincter pupillae muscles and the muscles of the ciliary body that control the
shape of the lens. The oculomotor nerve can be seen emerging from the walls of
the interpeduncular fossa between the cerebral peduncles of the midbrain. As it
emerges, it passes between the posterior cerebral and superior cerebellar arteries
before eventually passing into the orbit via the superior orbital fissure.
CN IV (trochlear nerve) -- This small, threadlike nerve supplies motor innervation
to the superior oblique muscle of the orbit. If present, it can be seen along the
lateral aspect of the cerebral peduncles near their junction with the ventral pons.
Neuroscience Laboratory Manual 46
It is the only cranial nerve to emerge from the dorsal aspect of the brainstem.
NOTE: Do not attempt to view this nerve on your brain specimens as it emerges
from the dorsal midbrain. This can be seen on demonstration. After emerging
just caudal to the inferior colliculi, it arches ventrally around the caudal midbrain
to dive between the layers of dura mater forming the anterolateral border of the
tentorial notch. It gains access to the orbit via the superior orbital fissure.
CN V (trigeminal nerve) -- This nerve supplies sensory innervation to the anterior
2/3 of the head, oral & nasal cavities and soft palate. In addition to supplying motor
and proprioceptive innervation to the muscles of mastication, it also supplies motor
and proprioceptive innervation to the mylohyoid, anterior belly of digastric, tensor
tympani and tensor veli palatini muscles. This large nerve emerges from the rostral
border of the middle cerebellar peduncle along the lateral aspect of the pons to
enter Meckel's cave, where the trigeminal (semilunar) ganglion resides. Distal to
the ganglion, CN V separates into its three divisions (ophthalmic, maxillary and
mandibular).
CN VI (abducens nerve) -- This nerve supplies motor innervation to the lateral
rectus muscle of the orbit. It can be found near the midline, emerging from the
inferior pontine sulcus at the ponto-medullary junction. It courses anteriorly to
gain access to the orbit via the superior orbital fissure.
CN VII (facial nerve) -- This complex nerve gives motor innervation to the muscles
of facial expression as well as the stapedius, posterior belly of the digastric and
stylohyoid muscles. In addition, preganglionic parasympathetic innervation is
supplied (via parasympathetic ganglia containing postganglionic neurons) to the
lacrimal gland, the submandibular and sublingual salivary glands, as well as the
mucous membranes of the hard palate, soft palate and nasal cavities. It also
contains sensory nerve fibers that convey taste from the anterior 2/3 of the tongue
and general sensation from the external ear. This nerve can be seen as it emerges
at the cerebellopontine angle. What foramen does it traverse to gain access to the
facial canal?
CN VIII (vestibulocochlear nerve) -- This sensory nerve conducts auditory
information from the cochlea and information for equilibrium from the
Neuroscience Laboratory Manual 47
semicircular canals. It emerges lateral to the facial nerve in the cerebellopontine
angle and enters the same foramen as the facial nerve.
CN IX (glossopharyngeal nerve) -- This nerve provides motor innervation to the
stylopharyngeus muscle. It also contains preganglionic parasympathetic nerve
fibers destined for the otic ganglion. Postganglionic fibers from this ganglion are
secretomotor to the parotid gland. The sensory nerve fibers in this nerve provide
taste and general somatic sensation from the posterior 1/3 of the tongue. It also
provides somatic sensation from the pharynx, palatine tonsils, middle ear and
visceral information from the carotid body and sinus. This nerve emerges from the
postolivary sulcus immediately caudal to CN VIII to pass into the jugular foramen.
CN X (vagus nerve) -- This nerve provides motor innervation to the muscles of the
pharynx (except stylopharyngeus), larynx and soft palate (except tensor veli
palatini). In addition, it provides preganglionic parasympathetic fibers to
parasympathetic ganglia that innervate smooth muscles and glands in the pharynx,
larynx and all thoracic and abdominal viscera down to the left colic flexure. It also
provides visceral sensory innervation to these same structures as well as taste to
the epiglottis and somatic sensory innervation to the external ear and external
auditory meatus. This nerve emerges from the postolivary sulcus immediately
caudal to CN IX as several compact rootlets arranged in a rostrocaudal fashion and
exits the skull via the jugular foramen.
CN XI (spinal accessory nerve) -- This nerve provides motor innervation to the
trapezius and sternocleidomastoid muscles. It will not be present on your
specimens, since it arises from the lateral aspect of the upper cervical spinal cord
to ascend through the foramen magnum and assume a position along the lateral
aspect of the medulla before it exits the skull through the jugular foramen.
CN XII (hypoglossal nerve) -- This nerve provides motor innervation to the intrinsic
and extrinsic muscles of the tongue. It exits the brainstem as a series of loosely
arranged rostrocaudal rootlets arising from the preolivary sulcus. These rootlets
converge to exit the skull via the hypoglossal canal.
Neuroscience Laboratory Manual 48
Slide Set
CN III (slides 24-22) -- Begin with slide 24. This is a horizontal section through the
rostral midbrain. The gray matter that lies dorsomedial to the red nuclei contains
the oculomotor nuclear complex. In addition, this nuclear complex contains two
small, almond shaped nuclei that lie on its dorsal aspect. These are the Edinger-
Westphal nuclei. What specific cell type is contained in the Edinger-Westphal
nuclei? Nuclei within the oculomotor nuclear complex gives rise to axons that
remain ipsilateral to form CN III on their respective sides. The boomerang shaped
white matter immediately lateral to the oculomotor nuclei is the medial
longitudinal fasciculus (MLF). This important fiber tract contains axons that
interconnect the motor nuclei of CN III, IV and VI. Can you speculate why these
nuclei should be interconnected?
On slide 23, find the above structures, including the emerging fibers of CN III along
the lateral walls of the interpeduncular fossa. As these fibers emerge from the
oculomotor nuclear complex, they fan out laterally and ventrally to pass through
the red nucleus before they swerve medially to exit the midbrain ventrally. This
phenomenon can be seen clearly on slide 22.
CN IV (slides 21,20) -- On slide 21, the trochlear nucleus replaces the Edinger-
Westphal nucleus just ventral to the periaqueductal gray. The small fascicle of
axons arising laterally from each nucleus is CN IV as it begins its journey to the
dorsal aspect of the pons by arching laterally and dorsally. The medial longitudinal
fasciculus can be seen just ventral to the trochlear nuclei and as a thin horizontal
strip across the midline. What specific level of the midbrain is represented in this
slide?
Slide 20 (rostral pons) is caudal to the trochlear nucleus, a structure of the
midbrain. However, it shows the fibers of CN IV in two perspectives: 1) as the
axons of CN IV arise from the trochlear nucleus, they turn caudally to form a tight
fascicle of fibers in the lateral reaches of the periaqueductal gray, and 2) upon
reaching the rostral pons, the fibers of CN IV cross the midline within the superior
medullary velum as the decussation of CN IV to emerge from the dorsum of the
brainstem as the contralateral CN IV. With this in mind, what clinical symptom(s)
Neuroscience Laboratory Manual 49
would you expect to see following a lesion of the right trochlear nucleus? Also note
the medial longitudinal fasciculus along the floor of the periaqueductal gray.
CN V (slide 18) -- Many of the major central components of this nerve have been
covered previously under the section entitled "Sensory Pathways for the Anterior
2/3 of the Head" (pp. 38-40). Go back and review that section now, then examine
the additional information below.
Slide 18 (middle 1/3 of pons) shows the central sensory and motor structures of V
with the exception of the spinal nucleus and tract of V, which reside at more caudal
levels. Reacquaint yourselves with the middle cerebellar peduncle, chief sensory
nucleus of V, and the mesencephalic tract and nucleus of V. Just medial to the
chief sensory nucleus of V is a small fascicle of nerve fibers, the motor root of V.
These fibers originated from the clear, egg shaped area, the motor nucleus of V,
located just medial to the motor root of V. This motor nucleus supplies the muscles
innervated by CN V. Do you remember what they are? Find the MLF on this slide.
CN VI and CN VII (slides 17-16) -- These three slides show the caudal 1/3 of the
pons. Slide 17 and slide 16 are essentially at the same level and show many of the
same structures. The floor of the fourth ventricle shows a groove at the midline,
flanked by gently sloping mounds called the facial colliculi. The clear oval areas
immediately subjacent to the facial colliculi are the left and right nuclei of CN VI. Is
this a motor or sensory nucleus? Arising from the medial surface of the nucleus of
CN VI, and coursing ventrally through the medial lemniscus, are the small fascicles
of axons forming CN VI. Just medial to the nucleus of CN VI lie two fasciculi, the
more dorsal one is the (internal) genu of CN VII. The other is the MLF. Note the
close proximity of the MLF and the nucleus of CN VI. The fascicle of axons arching
ventrolaterally from the lateral aspect of the floor of the fourth ventricle is CN VII.
Just medial to CN VII in the ventrolateral reaches of the pontine tegmentum is an
oval area, the motor nucleus of CN VII. What nucleus and its associated pathway
lie just lateral to CN VII in the pontine tegmentum? CN VII can also be seen
externally as it emerges just lateral to the ventral pons. A lesion of this nerve would
cause what clinical symptom(s)?
Neuroscience Laboratory Manual 50
At this point, it is critical to understand the internal path of axons arising from the
motor nucleus of CN VII. After arising from the nucleus, these axons travel
dorsomedially (cannot be seen here) to pass just caudal to the nucleus of CN VI and
lie at the floor of the fourth ventricle near the midline. At this point, they bend
rostrally (internal genu of CN VII) to ascend to the rostral pole of the nucleus of CN
VI. They then arch over the nucleus of CN VI and proceed ventrally and caudally to
exit the brainstem. How does this compare to the internal path of CN IV?
It should also be noted (but not seen) that the superior salivatory nucleus lies on
the dorsomedial aspect of each facial nucleus. This important autonomic nucleus
supplies preganglionic parasympathetic nerve fibers via CN VII that are
secretomotor to the lacrimal gland (via the pterygopalatine ganglion) and to the
submandibular and sublingual salivary glands (via the submandibular ganglion).
Slide 13, slide 10 and slide 9 illustrate the location of the nucleus and tractus
solitarius. On both sides, the dark “bulls eye” of white matter lying dorsomedial to
the spinal nucleus of V is the tractus solitarius, which is encircled by the lightly
stained nucleus solitarius. This nucleus and its related tract conduct primarily taste
information from CN VII, IX and X. These bilateral structures gradually approach
each other to fuse at the midline in the caudal medulla.
CN IX (slides 18-12,10,9) -- Begin with slide 14 (rostral medulla). On the right side,
CN IX can be clearly seen emerging from the postolivary sulcus. The pale area
immediately dorsomedial to the concavity of the postolivary sulcus contains the
nucleus ambiguus. This diffuse motor nucleus resides in the rostral medulla and
contributes axons to both CN IX and X. It supplies innervation to the muscles of
branchiomeric origin supplied by these two cranial nerves. If you are having
difficulty finding this nucleus, do not despair. It lives up to its name in that it is
difficult, at best, to pinpoint in any given section. You will have your best luck
finding it in slide 12 (light pink ovoid region).
In addition to this motor innervation, CN IX fibers from the inferior salivatory
nucleus also supply preganglionic parasympathetic fibers to the otic ganglion for
salivary secretions from the parotid gland. This small nucleus lies just medial to the
nucleus solitarius (don’t worry about trying to find it).
Neuroscience Laboratory Manual 51
Most of the efferent nerve fibers from the nucleus solitarius form the primary
ascending taste pathway, which is located primarily in the ipsilateral central
tegmental tract. Taste fibers in the central tegmental tract project to the thalamus
which, in turn, sends fibers to the postcentral gyrus near the Sylvian fissure (area
43) [gustatory neocortex] and the insula (see demonstration).
CN X (slides 12,10-8) -- Slide 12 shows CN X emerging from the postolivary sulcus
on the right side. The vagus nerve contains: 1) the shared contributions from the
nucleus ambiguus as previously described [see CN IX above], 2) taste and visceral
sensation fibers from visceral structures that use the tractus and nucleus solitarius,
and 3) somatic sensation fibers from the region of the external ear that enters the
spinal tract of V. In addition, it uniquely contains preganglionic parasympathetic
nerves fibers that supply viscera from the head down to the left colic flexure. These
axons arise from the dorsal motor (efferent) nucleus of X. The rostral extent of
this nucleus can be seen on slide 10; the clear area dorsomedial to the tractus and
nucleus solitarius is the dorsal motor nucleus of X. Now follow this nucleus to its
caudal extent (slide 9 and slide 8).
CN XI (slides 6,5) -- The motor nerve fibers innervating the trapezius and
sternocleidomastoid muscles arise from a special nucleus located in the upper 5 or
6 cervical spinal segments, called the (spinal) accessory nucleus. This nucleus can
be seen as a lateral extension of the ventral horn on slide 6 and slide 5. On slide 6,
observe the rootlets of the spinal accessory nerve lateral to the spinal cord.
CN XII (slides 10-8) -- This nerve contains motor nerve fibers to the intrinsic and
extrinsic muscles of the tongue. They arise from the hypoglossal nucleus, which is
located adjacent to the dorsal motor nucleus of X throughout its rostrocaudal
extent. On slide 10, locate the dorsal motor nucleus of X. Just ventromedial to
this nucleus is a round gray structure, the hypoglossal nucleus. On slide 9, axons
can be seen arising from the hypoglossal nucleus and traveling ventrally just lateral
to the medial lemniscus to emerge at the preolivary sulcus. Slide 8 shows the
caudal extent of the hypoglossal nucleus and a rootlet of CN XII emerging from the
preolivary sulcus (both sides).
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NEURORADIOLOGY
Slide 61 is an axial (cross sectional) view of an MRI through the ponto-medullary
junction, showing CN VI, as well as CN VII and VIII as they emerge from the
brainstem to enter the internal auditory meatus. The cochlea and the semicircular
canals can also be seen. Slide 62 is an axial view of an MRI through the midpons,
showing CN V as it emerges from the middle cerebellar peduncle and traverses the
subarachnoid space to enter into Meckel’s cave.
ANIMATIONS
Cranial nerves
DEMONSTRATIONS
Whole brain with cranial nerves
Dorsal view of brainstem showing CN IV
Half brains showing: Insula and Gustatory Neocortex
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NEUROROUND A 68-year old woman is brought to you by her son. He explains that his mother has lived by herself since the death of her husband 7 years ago. The son is concerned by her “condition” and thinks she can no longer live by herself. He states that she has deteriorated steadily during the last 6-9 months until she can no longer walk, use her right hand to feed herself, or talk clearly, and she has begun to drool. He shares his suspicions with you that she has probably had a series of small strokes and he fears she is becoming senile or demented. Your neurologic exam reveals the following:
1. A right sided hemiparesis with exaggerated deep tendon reflexes
2. A positive Babinski on the right side
3. Anesthesia of the left side of the face up to the vertex of the skull
4. She drools from the right side of her mouth, which droops noticeably, but she can raise both eyebrows.
5. Her speech is slurred.
6. When she opens her mouth to protrude her tongue to say “aah”, her jaw deviates to the left and her tongue deviates to the right.
You order an imaging study of the head and neck region, which shows an external mass compressing one area of the brain. In your diagnosis of this case, answer the following: 1. Identify the pathways/nuclei or other structures responsible for each
deficit/symptom.
2. Given the site of the lesion, are there any other symptoms you may have missed?
3. Given the site of the lesion and its cause, what radiologic technique would give the best results?
4. What types of extramedullary (extra axial) tumors are likely in this region of the brain?
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BASAL GANGLIA
Learning Objectives:
At the end of the laboratory session students will be able to:
1. List the main components of the basal ganglia, their location and their general “loop” connections as described in the lab manual and in lecture.
2. Identify the discrete motor deficits (i.e., dyskinesias) and cardinal signs that occur as a result of lesions to different regions of the basal ganglia as described in lecture.
___________________________________________________________________
The basal ganglia (also known as the "extrapyramidal system") are a group of
functionally and anatomically related subcortical nuclei, including virtually all parts
of the brain with the exception of the corticobulbar and corticospinal tracts.
Because the nomenclature for the basal ganglia can be confusing, the following
breakdown or nuclear groupings of the basal ganglia is presented to help alleviate
some of the confusion.
1. Corpus striatum
A. caudate nucleus
Striatum
B. putamen
Lenticular Nucleus
C. globus pallidus
2. Substantia nigra
3. Subthalamic nucleus
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The connections between 1) the nuclei of the basal ganglia and 2) the basal ganglia
and other brain centers are complex and their functional significance is unknown.
Consequently, we will condense them into a single, broad based, loop circuit as
follows: All areas of the cerebral cortex → via internal & external capsule →
striatum (caudate and putamen) and subthalamic nucleus → globus pallidus and
substantia nigra → VA, VL and DM nuclei of thalamus → via internal capsule →
all areas of cerebral cortex.
Although the basal ganglia per se do not project to the spinal cord, they connect
with structures that do (cortex, red nucleus). Through these connections, the basal
ganglia function to modulate and integrate somatic motor activity. Through its
input from virtually all areas of the cerebral cortex to the striatum and subthalamic
nucleus, and its subsequent output from the substantia nigra and globus pallidus
to the thalamus and back to the cerebral cortex, the basal ganglia act in concert
with the cerebellum as an interface between our sensory and motor systems.
Lesions of the various nuclei of the basal ganglia result in relatively discrete motor
deficits collectively called dyskinesias (abnormal involuntary movements).
REMINDER: Don’t forget that you should be able to name the discrete motor
deficits that arise as a result of lesions to different regions of the basal ganglia as
described in lecture.
Horizontal and Coronal Sections
Corpus Striatum (caudate, putamen and globus pallidus) and substantia nigra --
The caudate nucleus forms an incomplete ring around the dorsolateral and
ventrolateral aspect of the thalamus and is divided into three parts: head, body and
tail. The large head is located rostral to the thalamus, the body along the
dorsolateral aspect of the thalamus and the tail curves ventrolaterally to reside in
the roof of the inferior horn of the lateral ventricle. The tail terminates at the level
of the amygdala. The putamen and globus pallidus reside in the concavity of the
caudate nucleus, with the putamen located lateral to the globus pallidus (see Fig. 5
on next page). The substantia nigra is located in the midbrain tegmentum just
dorsomedial to the cerebral peduncles. The subthalamic nucleus lies ventral to the
thalamus at the junction of the midbrain and diencephalon (this structure will be
seen on slides).
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On your coronally sliced brain specimen, select a section just rostral to the anterior
commissure. The nuclear mass forming the lateral wall of the frontal horn of the
lateral ventricles is the head of the caudate nucleus. Just ventrolateral to the
anterior limb of the internal capsule is the putamen. On the next section caudally,
the head of the caudate nucleus remains in the same position if the thalamus is not
present. However, the putamen is typically joined medially at this level by the
globus pallidus. The next section caudally should contain the thalamus. If so, the
head of the caudate nucleus has been replaced by the body of the caudate nucleus.
If the inferior horn of the lateral ventricle can be seen in the temporal lobe, find
the small tail of the caudate nucleus in the roof of the inferior horn of the lateral
ventricle. Follow and identify the body and tail of the caudate nucleus, putamen
and globus pallidus in subsequent sections. On some of your specimens, the
coronal cuts may go far enough caudal that the midbrain has been cut in frontal
section. If so, try to find a black-pigmented region in the midbrain tegmentum.
This is the substantia nigra. What causes the black pigmentation of this region?
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Select a horizontal section just ventral to the body of the corpus callosum. (NOTE:
As you go through your horizontal sections, correlate and compare what you see
with the same structures in the coronal sections. This will help you get a better
understanding of the three-dimensional anatomy of the basal ganglia). Identify the
head and body of the caudate nucleus on this section, if possible. On more ventral
sections, identify the head and tail of the caudate nucleus, putamen and globus
pallidus. In addition, if the most ventral cut goes through the midbrain, the
substantia nigra can be seen as a black-pigmented region just dorsomedial to the
cerebral peduncles. If your specimen does not show this, look on your neighbor's
specimen and/or look at the demonstrations.
Slide Set
Begin with slide 21. The substantia nigra can be seen at this and all midbrain levels
as a pale nuclear region dorsomedial to the cerebral peduncles. Follow the
substantia nigra rostrally (slide 22, slide 23, slide 24, slide 25, and slide 28).
Lesioning the substantia nigra produces what clinical malady? Note the body and
tail (left side) of the caudate nucleus in slide 26, and a close-up of the tail of the
caudate nucleus in the roof of the temporal horn of the lateral ventricle on slide
27.
As the transition zone between the midbrain and diencephalon is reached (slide
25, slide 29, slide 30 and slide 31), the subthalamic nuclei appear dorsal to the
substantia nigra as fusiform tapered structures resembling cat's eyes. A lesion of
the right subthalamic nucleus would produce what SPECIFIC clinical symptom(s)?
On slide 31, the globus pallidus can be seen. Some of the dark bundles of fibers
running diagonally dorsal to subthalamic nucleus represent output pathways from
the globus pallidus and the substantia nigra, that are primarily destined for VL of
the thalamus. Also find the putamen and body of the caudate nucleus on this slide
and note the relationship between the globus pallidus and internal capsule.
On slide 33 and subsequent slides (slide 34, slide 35 (horizontal), slide 36
(horizontal), and slide 37), identify the caudate nucleus, putamen and the globus
pallidus, where possible. Slide 35 shows the fusion of the head of the caudate
nucleus and putamen at the rostral extent of the anterior limb of the internal
capsule.
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NEURORADIOLOGY
Slide 47 and slide 48 show the head of the caudate nucleus and the putamen. In
addition to the above structures, slide 49 also shows the globus pallidus. Slide 50
reveals the substantia nigra (NOTE THE ORIENTATION OF THE MIDBRAIN).
ANIMATIONS
Caudate nucleus
Striatum
Subthalamic nucleus – Substantia nigra.
DEMONSTRATIONS
Caudate nucleus
Amygdala
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NEUROROUND
A family brings in their 67-year old father to the clinic for evaluation. The patient’s daughter notes their concern that “old age seems to be creeping up on Dad rather quickly the last few months.” She goes on to describe how he is slowing down. His wife complains that it often takes forever for him to get dressed and shave in the morning. She states she used to be a nurse and is concerned that he is becoming demented. His son states that when they get out of the car they have to tell him to get out or “he might just sit there forever.” Additionally, he notes a peculiar habit where if his father smiles during a conversation, it just seems to get stuck and stays there well after the topic has moved on. The family is concerned over his state and voices their concern that “Dad may not be ‘all there’.” During all of this, the patient says nothing and moves little. When you ask the patient to get up out of his chair and follow you into the exam room, he stands up then goes nowhere. He simply stands by the chair. After coaxing him to follow, you begin your physical exam. The exam shows an elderly appearing male appearing a bit older than his stated age. He has a stooped posture. His affect is rather flat and his face expressionless. A very slight tremor of his right hand is noted at rest. Pertinent neurological findings are as follows:
1. CN’s II - XII intact
2. No Babinski or clonus elicited
3. Muscle strength equal bilaterally
4. “Cogwheel rigidity” noted upon flexing and extending each elbow, especially on the patient’s right side.
5. Very slight tremor of the right hand at rest which ceases during finger to nose movements.
6. No significant problems with rapidly alternating movements of the hands; no ataxia in walking; no imbalance with eyes closed; normal finger to nose test.
7. Patient answers questions appropriately. Knows name, date, year, president and knowledgeable of current events.
In your diagnosis of this case, answer the following:
1. What are the three cardinal signs of this patient’s disease? Other manifestations?
2. Discuss the pathways and deficiencies involved.
3. Discuss how pharmaceutical treatment of this disease relates to #2.
4. When symptoms become refractory to medications after long-term treatment, what alternative therapeutic options are available for treatment of this disease?
5. What is the significance of the absence of a Babinski or clonus?
6. What is the significance of the lack of ataxia or problems with finger to nose test or rapidly alternating movements?
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CEREBELLUM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the gross anatomy of the cerebellum and its positional relationship to the cerebrum and brainstem.
2. List the functions of the cerebellum as described in the lab manual and in lecture.
3. Appreciate the functional/clinical consequences of cerebellar lesions.
4. Discuss the blood supply to the cerebellum.
___________________________________________________________________
The cerebellum (L., little brain) straddles the dorsal aspect of the brainstem. Within
the skull, it resides in the posterior cranial fossa immediately inferior to the
tentorium cerebelli. It is attached to the brainstem by three paired nerve fiber
bundles called cerebellar peduncles. It is through these peduncles that the
cerebellum communicates and interacts with other regions of the CNS. By way of
these connections, the cerebellum has a profound effect on equilibrium, posture,
muscle tone and the coordinated, synergistic muscle contractions required for the
meaningful execution of a variety of tasks including walking, speech, eye
movements, writing, playing musical instruments, etc. The role of the cerebellum
is not to initiate these movements per se, but to insure that these movements,
when initiated, are smooth, purposeful and coordinated. NOTE: Voluntary
movements (via corticospinal and/or corticobulbar tracts) can be made without
cerebellar involvement, but the result is clumsy, disorganized movement
(dyssynergia/cerebellar ataxia).
GROSS ANATOMY – Whole and Half Brains
On your whole brains, observe the cerebellum from the dorsal (posterior) side. The
superior surface of the cerebellum is flattened and tucked beneath the occipital
lobes of the cerebral hemispheres. Gently separate the cerebellum and occipital
lobes to view the superior surface of the cerebellum. The midline vermis is
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elevated on the superior surface with the cerebellar hemispheres gently sloping
laterally. Near the middle of the superior surface of the cerebellum is a transverse
crease called the primary fissure. It is best seen on demonstration or on your half
brains. This fissure divides the cerebellum into anterior and posterior lobes. Do
not confuse this fissure with the horizontal fissure, which runs along, or just
inferior to, the lip of cerebellum that separates the superior and inferior surfaces.
Note the blood vessels ramifying on the superior surface. These are branches of
the superior cerebellar arteries and their corresponding veins.
In contrast to the superior surface, the inferior surface of the hemispheres is
convex. The midline vermis is depressed and hidden from view, forming the floor
of a deep crevice, the posterior median fissure. The falx cerebelli resides in this
fissure when the brain is in the skull. Near the midline inferiorly, the cerebellum
surrounds the dorsolateral aspect of the medulla with two swellings, the cerebellar
tonsils. Occasionally, the cerebellar tonsils are useful in diagnosing elevated
intracranial pressure, since they tend to herniate through the foramen magnum as
a result of this condition. Two named blood vessels supply the inferior surface of
the cerebellum. Their origin and distribution can be highly variable and
considerable overlap of territories is not uncommon. The posterior inferior
cerebellar arteries typically arise from the vertebral arteries. They arch dorsally
around the medulla, giving off small branches to the lateral medullary region, then
continue to ramify on the inferior surface of the cerebellum posterior to the tonsils.
The anterior inferior cerebellar arteries typically arise from the basilar artery to
pass laterally over the cerebellopontine angle and ramify on the inferior surface of
the cerebellum anterior to the tonsils. Just lateral to the cerebellopontine angle is
a slender lateral projection of cerebellar tissue, the flocculus (part of the
flocculonodular lobe). The posterolateral fissure extends laterally from the
posterior aspect of the flocculus and separates the flocculonodular lobe from the
posterior lobe.
Two of the three cerebellar peduncles can be seen on the ventral surface of your
whole brain specimens. The large middle cerebellar peduncle (brachium pontis)
lies rostral to the flocculus. Medial to the flocculus, find the inferior olive and
postolivary sulcus. The rounded mass dorsal to the postolivary sulcus is the
inferior cerebellar peduncle (restiform body). The above two peduncles transmit
primarily afferent nerve fibers to the cerebellum.
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Now look at the medial surface of your half brain specimen (see Fig. 6 below). The
cut was made through the midline, bisecting the vermis.
The cut midline surface of the cerebellum has the appearance of trees with leaves,
called folia, sprouting along the extent of their branches. Like the cerebral cortex,
the neurons of the cerebellar cortex lie at the surface in the folia and "branches" of
white matter converge in the deeper regions of the cerebellum to form "trunks"
that merge to form the deep white matter that constitutes the roof of the fourth
ventricle. Imbedded in this deep white matter are the deep cerebellar nuclei (to
be seen on slides). The cerebellar cortex at the vermis is separated into nine lobules
(identification of some lobules is provided for anatomical reference, not
examination purposes). The deep groove between the culmen and declive along
the superior surface of the vermis is the primary fissure, which separates the
anterior and posterior lobes. Being careful not to tear any tissue, follow this fissure
onto the superior surface of the cerebellum. The groove between the nodule (the
central part of the flocculonodular lobe) and the uvula along the inferior surface of
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the vermis is the posterolateral fissure. Note the cerebellar tonsil just inferior and
lateral to the uvula.
Now find the superior medullary velum, which forms the roof of the fourth ventricle
at its rostral extent. The relatively thick wall of the fourth ventricle at this level is
formed by the superior cerebellar peduncle (brachium conjunctivum). This
peduncle is the primary pathway for efferents from the cerebellum.
Functional subdivisions of the cerebellum -- Now that you have some knowledge of
the gross anatomy of the cerebellum, we can separate it into its functional
subdivisions (as described in lecture).
1. Vestibulocerebellum (archicerebellum) -- consists of the flocculonodular lobe
a. FUNCTION: EQUILIBRIUM, REGULATION OF EYE MOVEMENT
2. Spinocerebellum (paleocerebellum) -- consists roughly of the vermis and
paravermal zones (just lateral to the vermal region), including the tonsil.
a. FUNCTION: MUSCLE TONE, STEREOTYPIC MOTOR ACTIVITY (WALKING,
STANDING, SWIMMING, ETC.)
3. Pontocerebellum (neocerebellum; cerebrocerebellum) -- consists of the lateral
hemispheric zones.
a. FUNCTION: MOTOR COORDINATION OF NON-STEREOTYPED (LEARNED, SKILLED) MOVEMENTS
AFFERENT AND EFFERENT CONNECTIONS – Slide Set
There are a number of afferent and efferent pathways for the cerebellum. To list
and/or discuss all of them would serve no useful purpose. Instead, we will
concentrate on those pathways that can readily be assigned a function that will
help in understanding how the cerebellum works through its interconnections with
other regions of the CNS.
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Afferent Connections -- The cerebellum receives afferents from the spinal cord and
brainstem. These afferents will be studied in an ascending fashion, beginning with
the spinal cord.
1. Spinal cord -- In contrast to the dorsal column and spinal lemniscus pathways
which transmit conscious information, spinal cord pathways to the cerebellum
transmit the unconscious modalities of proprioception, touch and pressure
impulses via the inferior cerebellar peduncle to the vermal and paravermal
regions of the cerebellum.
2. Brainstem -- Brainstem afferents arise primarily from three sources:
A. pontine nuclei; B. vestibular nuclei; C. inferior olivary nuclei.
A. (Cortico)-ponto-cerebellar pathway -- Axons from the cerebral cortex
project to the ipsilateral pontine nuclei via the cerebral peduncles. The
pontine nuclei then project their axons to the contralateral cerebellar cortex
(lateral region of posterior lobe) via the middle cerebellar peduncle.
B. Vestibulocerebellar tract -- From the vestibular nuclei via the juxtarestiform
body to the flocculonodular lobe.
C. (Cortico)-olivo-cerebellar pathway -- Axons from the cerebral cortex project
to the inferior olivary nucleus (complex). Cells in the inferior olivary complex
then project axons contralaterally to all areas of the cerebellar cortex via the
inferior cerebellar peduncle.
Begin with slide 19. The cerebral cortex provides axons to the ventral pontine
nuclei via the cerebral peduncles. The pontine nuclei within the ventral pons give
rise to axons that cross the midline and project via the large middle cerebellar
peduncle to the lateral hemispheres of the posterior lobe. Identify the above
structures on slide 18, slide 17 and slide 16.
There are four pairs of vestibular nuclei within the medulla and pons. These nuclei
provide afferent fibers to the flocculonodular lobe of the cerebellum via the
juxtarestiform body (slide 16 and slide 15), which lies in juxtaposition (medial) to
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the restiform body (inferior cerebellar peduncle). (It should also be noted that this
pathway carries efferent fibers from the cerebellum to the vestibular nuclei).
The inferior olivary nucleus projects axons to the cerebellum via the contralateral
inferior cerebellar peduncle. Begin with slide 15, which is at the level of the ponto-
medullary junction and observe the following: The left and right inferior olivary
nuclei each project their axons to the contralateral cerebellar cortex by sending
them medially to decussate through the medial lemniscus and continue through
the contralateral inferior olivary nucleus to arch dorsolaterally where they enter
the contralateral inferior cerebellar peduncle. This can be seen clearly on slide 13
and slide 12.
Efferent Connections -- In contrast to the diffuse origin of afferent
connections/pathways to the cerebellum, the vast majority of axons exit the
cerebellum via the superior cerebellar peduncle. To understand this concept,
consider that the input to the cerebellum comes from a wide variety of structures
and travels to all regions of the cerebellar cortex via three peduncles. The output
from the cerebellar cortex is also diffuse. However, the vast majority of these cells
do not project their axons outside the confines of the cerebellum, but instead send
them to converge and synapse on the four pairs of deep cerebellar nuclei, which
are located within the white matter in the roof of the fourth ventricle. This
relatively compact set of nuclei gives rise to axons that pass primarily through the
superior cerebellar peduncle. Because of this compact anatomical arrangement,
small lesions to this region (deep cerebellar nuclei, superior cerebellar peduncle)
can produce profound effects.
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Deep cerebellar nuclei -- Look at slide 10. The deep cerebellar nuclei are located
within the deep white matter of the cerebellum overriding the caudal pons and
medulla. They are, from lateral to medial:
1. dentate nucleus -- receives afferents from the Purkinje cells of the lateral
hemispheres.
2. emboliform nucleus nucleus interpositus; receives afferents from the Purkinje cells of the paravermal region.
3. globose nucleus
4. fastigial nucleus -- receives afferents from the vermis and flocculonodular
lobe.
Now find the above nuclei on slide 11 and slide 14. The fastigial nucleus projects
its axons to vestibular nuclei via the juxtarestiform body. Axons from the remaining
deep cerebellar nuclei exit the cerebellum via the superior cerebellar peduncle
(slide 16 and slide 19). Slide 20 and slide 21 illustrate how the superior cerebellar
peduncle arches ventromedially to decussate (decussation of the superior
cerebellar peduncle) at the levels of the rostral pons and caudal midbrain. After
decussating, these axons pass through the contralateral red nucleus (slide 22, slide
23). Some of these axons terminate in the red nucleus which, in turn, gives rise to
axons that decussate immediately and descend to the spinal cord as the
rubrospinal tract. This pathway, which provides excitatory motor innervation
primarily to the flexor muscles of the upper extremity, can be seen as rounded
projections from the ventral surface of the decussation of the superior cerebellar
peduncle on slide 21.
Other axons from the deep cerebellar nuclei pass through the red nucleus and
ascend to terminate in the ventrolateral (VL) nucleus of the thalamus (slide 31 and
slide 32). The VL gives rise to axons that project to the cerebral cortex (Brodmann's
areas 4 and 6). This pathway provides information to the cerebral cortex
concerning the location of the body in space to ensure smooth coordinated
movements.
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Thus, the cerebral cortex forms loop circuits with the cerebellum as follows:
cerebral cortex → via int. capsule & cerebral peduncles → pontine & inf. olivary
nuclei → via middle & inf. cerebellar peduncles → cerebellum → via sup.
cerebellar peduncle → VL of thalamus → via int. capsule → cerebral cortex. Can
you recall a pathway or pathways involving the basal ganglia that are similar or
have common elements to those of the cerebellum?
Cerebellar Pathology -- There are 4 important concepts to keep in mind when
considering lesions of the cerebellum. These concepts are as follows:
1. Lesions of the cerebellum or its afferent or efferent pathways may disrupt
normal coordinated movements, but will not cause paralysis.
2. Each cerebellar hemisphere exerts its influence on the muscles of the
ipsilateral side of the body. Can you justify this statement anatomically?
3. The flocculonodular lobe influences the axial musculature bilaterally.
4. Lesions of the efferent pathway (deep nuclei and/or superior cerebellar
peduncles) produce more profound and permanent deficits than do lesions of
the afferent pathways or cerebellar cortex.
NEURORADIOLOGY
On slide 45, find the anterior and posterior lobes, and primary fissure. On slide
46, identify the middle and (decussation of the) superior cerebellar peduncles.
Slide 54 and slide 55 show cerebellar pathology. What lobe(s) of the cerebellum is
(are) involved? What artery provides the major blood supply to the region of the
cerebellar pathology? On slide 60, find the cerebellar tonsils. Slide 61 shows the
cerebellar vermis. On slide 62, find CN V emerging from the middle cerebellar
peduncle. On slide 63, both the middle and superior (adjacent to 4th ventricle)
cerebellar peduncles can be seen.
DEMONSTRATIONS
Cerebellum -- cerebellar peduncles, cerebellar fissures (primary, horizontal,
posterolateral).
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NEUROROUND
CC: 7 y/o presenting with headache, nausea and vomiting HPI: This 7 year old is brought to you by his parents who report a 2 week history of worsening
morning headaches and occasional vomiting. He had a low grade fever earlier in the week. When seen a few days ago at a local acute care clinic, they were told that he had gastroenteritis. Fluids and suppositories for the vomiting were prescribed. His condition has worsened since then. At times he is somewhat listless. The headaches have not improved and the vomiting is becoming more frequent, now up to 5 times per day. This morning his mom reported his “feeling dizzy” and that he stumbles when he walks.
PE: Acutely ill-appearing 7 year old male. Vital signs normal except for T - 99.5.
HEENT: Pupils equally round and reactive to light. Extraocular movements show questionable difficulty abducting each eye. Fundiscopic exam shows papilledema bilaterally. Nose and throat are clear.
Chest: Heart normal rate and rhythm with no murmurs. Lungs clear.
Abd: No organomegaly, pain to palpation, masses or bruits. Bowels sounds are normal.
Neuro: CN’s II - XII intact except for difficulty abducting eyes when to told look laterally. Nystagmus noted on careful examination of the eyes. Gait is ataxic with poor balance. Poor finger to nose test. Rapidly alternating movements of the hands are disordered. Poor check and rebound.
Summary: 7-year old with papilledema and vomiting and neurological changes as noted. In your diagnosis of this case, answer the following: 1. What is papilledema and what is its significance in a neurological exam?
2. How do the neurological signs help to pinpoint the location of the problem?
3. What signs and symptoms distinguish this patient’s problems as having a neurological basis, rather than gastrointestinal as first thought?
4. What are the diagnostic possibilities?
5. Why the difficulty with abduction of the eyes?
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VESTIBULAR SYSTEM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Identify the vestibular nuclei and relate the functional significance of their connections with extraocular nuclei, cerebellum and spinal cord.
2. Demonstrate how the vestibular system is tested and the normal behavioral consequences of the testing procedures.
3. Discuss the CNs and pathways involved in vestibulo-ocular reflexes.
___________________________________________________________________
CN VIII (vestibulocochlear nerve) -- As the name implies, the vestibulocochlear
nerve has two primary functions: equilibrium (vestibular portion) and hearing
(cochlear portion). As such, each division of this nerve has discrete external
structures as well as discrete internal nuclei and pathways within the brainstem
that serve each of these modalities. In this laboratory session, we will identify the
central nuclei and pathways that serve the vestibular division of CN VIII.
Peripherally, hair cells within the ampullae of the semicircular canals, utricle and
sacculus are connected with the peripheral processes of the primary vestibular
afferents. The cell bodies for these primary afferents are located in the vestibular
(Scarpa's) ganglion, which resides in the internal auditory meatus. A few of the
central processes of these ganglion cells project directly to the flocculonodular lobe
via the juxtarestiform body. However, the vast majority of these central processes
project to the ipsilateral vestibular nuclei located in the pons and medulla. The
vestibular nuclei give rise to axons that project to spinal cord, cerebellum,
extraocular motor nuclei, vestibular nuclei and thalamus. Efferents from the
vestibular nuclei to the thalamus are relayed to the postcentral and superior
temporal gyri.
Vestibular division of CN VIII -- Beginning with slide 15, locate the inferior
cerebellar peduncle. Note: You should know the general location of the
vestibular nuclei, however, you do not need to know the specific name and be
able to individually identify each one. The "salt and pepper" or speckled region
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dorsomedial to the inferior cerebellar peduncle identifies the inferior (spinal)
vestibular nucleus. Medial to the inferior vestibular nucleus lies the medial
vestibular nucleus. On subsequent rostral slides, the inferior vestibular nucleus is
replaced by the lateral vestibular nucleus. The slender dorsolateral extension of
gray matter from the lateral vestibular nucleus is the superior vestibular nucleus.
Notice on the left side how the fibers of the juxtarestiform body intermingle with
medial and inferior vestibular nuclei. Identify the medial longitudinal fasciculus
(MLF) in the midline at the floor of the fourth ventricle. At this level, the MLF
contains: 1) ascending axons from the vestibular nuclei to the extraocular motor
nuclei (CN III, IV, VI) for coordinating eye movements during the process of
maintaining equilibrium and 2) descending bilateral axons from the medial
vestibular nuclei for control of somatic muscles in maintaining equilibrium. Identify,
where possible, the above structures on slide 13, slide 12 and slide 10.
Using your brain atlas and slide 16, slide 17 and slide 18, follow the MLF and the
vestibular nuclei rostrally to get a feel for their location and rostrocaudal extent.
As you proceed, also observe the juxtarestiform body on slide 16. How far rostrally
would you expect to find the MLF and why?
NEURORADIOLOGY
On slide 61, find CN VII & VIII emerging from the cerebellopontine angle. Also find
the internal auditory meatus and the semicircular canals.
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AUDITORY SYSTEM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the anatomy and function of the central and peripheral structures that comprise the auditory system.
2. Compare the differences in symptoms between central and peripheral lesions of the auditory system.
___________________________________________________________________
Auditory information is transmitted to the CNS via the auditory division of CN VIII
(vestibulocochlear nerve). Peripherally, hair cells within the cochlea are in synaptic
contact with the peripheral processes of the spiral ganglion cells, which are located
in the bony modiolus. The central processes of these cells form the cochlear
division of CN VIII.
Observe slide 40. This is a cross section through the cochlea. A brief summary of
the spatial organization of the cochlea is provided for reference in locating neural
components, although you should be familiar with this information from the
corresponding Histology laboratory. The large space at the top of the slide is the
scala vestibuli (contains perilymph). The diagonal membrane is called the
vestibular (Reissner's) membrane. This structure separates the scala vestibuli and
the scala media (cochlear duct). The latter contains endolymph. The cavity at the
bottom of the slide is the scala tympani which is continuous with the scala vestibuli
at the apex of the cochlea. As such, it contains perilymph. The large structure on
the left (modiolus) forms a shelf-like process called the bony spiral lamina. At the
tip of the shelf, the basilar membrane stretches to the right to make contact with
the spiral ligament which attaches to the outer region of the bony labyrinth (not
seen). Resting on the basilar membrane is the (spiral) organ of Corti. Above the
basilar membrane at approximately its midpoint, a row of three slender cells can
be seen. These are the outer hair cells. Just to the left of these cells is the fusiform
space called the space of Nuel. The space just to the left of the space of Nuel is the
(inner) tunnel of Corti, which is bounded on the left and right by the inner and outer
columns respectively. The inner hair cells reside at the tip of the inner column. In
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this plane of section, there are typically one row of inner hair cells and 3 rows of
outer hair cells. The next space to the left is the internal spiral sulcus. The roof of
this sulcus is formed by the translucent tectorial membrane, which extends to the
right to make contact with the apical hairs of the inner and outer hair cells. The
hair cells are in contact with the peripheral processes of the spiral ganglion cells,
which gain access to the hair cells via the bony spiral lamina. The spiral ganglion
resides in the modiolus and contains the primary afferent cell bodies in the auditory
pathway.
Vibration of the foot of the stapes on the oval window creates displacement of the
basilar membrane. This phenomenon produces a shearing effect between the
tectorial membrane and the hair cells. When the hairs are displaced because of
the shearing forces, the hair cells stimulate the spiral ganglion to transmit impulses
into the CNS via the auditory division of CN VIII.
To locate the central auditory pathways, begin with slide 15. On the right side, just
lateral to the inferior cerebellar peduncle, there is a large region of mottled gray
matter, the ventral cochlear nucleus. Immediately ventral to this nucleus is the
darkly stained region of CN VIII as it emerges from the cerebellopontine angle. The
clear nuclear area along the dorsal aspect of the inferior cerebellar peduncle is the
dorsal cochlear nucleus. Identify, where possible, the above structures on slide 14,
slide 13 and slide 12.
Now follow the auditory pathway as it ascends through the brainstem. Beginning
with slide 15, note the ventral cochlear nucleus and CN VIII on the right side. The
dorsal and ventral cochlear nuclei contain the 2o auditory neurons. Some of the
crossed fibers of the ventral cochlear nucleus synapse in the contralateral superior
olivary nucleus (SOLN), which can be seen on slide 16. This nucleus is located just
lateral to the central tegmental tract and is shaped like an inverted "V". The
majority of axons arising from the SOLN enter the ipsilateral lateral lemniscus,
which lies just lateral to the SOLN. Find the SOLN, and lateral lemniscus in slide 17.
Follow the lateral lemniscus rostrally as it fans out to assume a vertical orientation
in the lateral wall of the rostral pons (slide 18, slide 19 and slide 20). On slide 20
(right side), the lateral lemniscus is split into medial and lateral portions by the
nucleus of the lateral lemniscus, another relay nucleus in the auditory pathway.
On slide 21, the nerve fibers of the lateral lemniscus can be seen sweeping medially
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to innervate the ventrolateral aspect of the nucleus of the inferior colliculus.
Axons arising from the nucleus of the inferior colliculus emerge from the
dorsolateral aspect of the nucleus to ascend along the lateral wall of the rostral
midbrain as the brachium of the inferior colliculus (slide 22). Follow the brachium
of the inferior colliculus rostrally as it enters and synapses within the ipsilateral
medial geniculate (body) (slide 23, slide 25, and slide 28). Axons arising from the
medial geniculate body project to the dorsal aspect of the superior temporal gyrus
called the transverse temporal gyrus (of Heschl) (Brodmann's areas 41,42). NOTE:
THIS CAN BE SEEN ON DEMONSTRATION.
Given the external and internal anatomy of the auditory system, would a unilateral
lesion of the lateral lemniscus in the midbrain produce ipsilateral loss of hearing? If
not, what symptom(s) would you expect from this lesion and why? Where would a
lesion of the auditory pathway produce total loss of hearing in the left ear?
NEURORADIOLOGY
On slide 61, find CN VII & VIII, the internal auditory meatus and the cochlea.
ANIMATION
Auditory radiations (transverse temporal gyrus).
DEMONSTRATIONS
Half brain showing: Auditory cortex (transverse temporal gyrus).
Dorsal view of brainstem showing: inferior colliculus, brachium of inferior
colliculus, medial geniculate.
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VISUAL SYSTEM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Review the functional anatomy of the globe of the eye as learned in Gross Anatomy and Histology.
2. Identify all fiber tracts and cortical structures associated with the visual system.
3. Trace the central visual pathway and describe the consequences of lesions along its course.
4. Describe the pathway of pupillary light reflexes with emphasis on direct vs. consensual light responses.
___________________________________________________________________
The visual system is a delicately balanced, highly complex system that enables us
to see our environment in great detail, and in color. The act of "seeing" or
visualizing an object occurs in two phases: The first phase involves light reflecting
from an object and passing into the globe of the eye via the cornea. Within the
eye, the lens directs and focuses the light onto a specialized region at the back of
the eye called the retina. The second stage of visualization is the conversion of this
light energy into electrical impulses by the retina. Ganglion cells within the retina
give rise to axons that form the optic nerve. Visual information that has been
processed by the retina is transmitted through the optic nerve to the optic chiasm
where some axons enter the hypothalamus to influence diurnal rhythms. The
majority of nerve fibers enter the optic tracts, which project axons to the primary
visual cortex in the occipital lobe via a relay in the lateral geniculate body of the
thalamus. The primary visual cortex then relays this visual information to other
areas of the cerebral cortex for further processing and analysis. Some of the optic
tract fibers bypass the lateral geniculate to project into the rostral midbrain where
they provide the input for visual reflexes (pupillary dilation and constriction,
accommodation and eye movements in response to visual stimuli).
Globe of the eye (slides 41-44) -- We will begin our study of the visual system by
examining the globe of the eye. Slide 44 shows a low power view of a horizontal
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section cut through the equator of the eye. Find the cornea, anterior chamber,
iris, lens, posterior chamber, ciliary body and ciliary processes. Now turn to slide
41 and identify these same structures on this higher power view. Also observe the
pigmented layer of the iris on this slide. What effect does contraction of the
muscles of the ciliary body have on the tension applied to the lens? What effect
does this have on the shape of the lens? Would a lesion of the superior cervical
sympathetic ganglia have any effect on the shape of the lens? Why (or why not)?
Now turn back to slide 44 and identify the vitreous chamber, retina, optic disc,
central artery to the retina, optic nerve and dura mater, arachnoid mater and
subarachnoid space. Can you explain why the optic nerve is surrounded by
meninges? Slide 43 is a high power view of the macula lutea, the region of the
retina that produces the best visual acuity, and the posterior wall of the eye. Note
the three visible cell layers of the retina, the visual receptor cells (rods and cones),
bipolar cells and ganglion cells. The depressed area at the center of the macula
lutea is the fovea centralis. What is the unique feature of this region? Also identify
the pigment layer of the retina, the choroid layer and the sclera. Between what
layers does retinal detachment occur? Why is it important to reattach the retina as
soon as possible? Now observe slide 42. This is a high power view of the optic disk
and optic nerve. Why is the optic disk called the "blind spot"? Where are the cell
bodies of origin for the nerve fibers in the optic nerve? Nerve fibers arising from the
nasal (medial) half of the retina cross to the contralateral side of the brain via the
optic chiasm. The remaining nerve fibers from the temporal (lateral) half of the
retina remain ipsilateral.
The remainder of the visual pathway can be seen on slides 23-26,28,29,31-33 and
in the animation. To better understand the plane of section on each of these slides,
compare each slide with your half brain specimen. For example, look at slide 33.
At the bottom of the slide in the midline is a small part of the infundibulum. Find
this structure on your half brain just posterior to the optic chiasm. Approximately
in the middle of the slide is the massa intermedia. Find this structure on your half
brain. Now draw an imaginary line between the infundibulum and the massa
intermedia. This is the plane of section on slide 33. Note the optic tract (slide 33
and slide 32) just lateral to the hypothalamus. Follow the optic tract posteriorly as
it diverges to lie just ventral to the cerebral peduncles (slide 31 and slide 29). On
slide 28 and slide 26, the optic radiations can be seen emerging from the
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dorsolateral aspect of the lateral geniculate bodies as they head for the primary
visual cortex (area 17). Slide 25 reveals the optic chiasm, and optic tract
innervating the lateral geniculate (on left side). The fibers of the brachium of the
superior colliculus can be seen after they exit the optic tract to wind around the
dorsal aspect of the medial geniculate just ventral to the pulvinar to enter the
pretectal area. Some of these fibers cross the midline in the posterior commissure.
What is the function of this pathway? The brachium of the superior colliculus, optic
tract, lateral geniculate and optic radiations can also be clearly seen on slide 23.
Coronal and Horizontal Sections; Half Brain
Coronal sections -- Starting with the section through (or near) the optic chiasm,
follow the optic tracts caudally and attempt to find the lateral geniculate bodies
and note the optic radiations emerging from the lateral geniculate bodies.
Horizontal sections -- Select the section that contains the anterior commissure and
if possible, find the medial and lateral geniculate bodies. This section should also
reveal the optic radiations. It should be noted at this time that axons within the
optic radiations that serve the upper visual fields (lower retinal fields) travel
rostrally from the lateral geniculate nuclei to loop around the rostral pole of the
temporal horn of the lateral ventricles before they turn caudally to join the
remaining optic radiations and terminate in the primary visual cortex.
Consequently, lesions of the temporal lobe may result in visual field deficits. This
indirect pathway is called Meyer’s loop. On the section immediately ventral to this
one, try to find the optic tracts as they wind around the brainstem just anterior
(ventral) to the cerebral peduncles. NOTE: Whether you see some of these
structures will rely on the "luck of the cut". If you are unable to see the above
structures on your sectioned brains, look on the brain specimens of one of your
neighbors.
Half brain -- On the medial surface, find the parietooccipital sulcus and the
calcarine sulcus. The cortex surrounding the dorsal and ventral lips of the calcarine
sulcus is the primary visual cortex (area 17), which receives afferents from the
lateral geniculate bodies. A good portion of the primary visual cortex is hidden
from view, since the calcarine sulcus extends laterally into the occipital cortex. The
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general cortical region dorsal to the calcarine sulcus is the cuneus. Its counterpart
ventral to the calcarine sulcus is the lingula.
NEURORADIOLOGY
Find the optic nerve, optic chiasm, calcarine fissure, cuneus and lingula on slide
45. Can you find the lateral geniculate bodies on slide 46? (Hint: Compare this
slide with your coronal brain specimens). The optic radiations can be clearly seen
on slide 47, slide 48 and slide 49. A lesion of the optic radiations on the right side
would cause what clinical symptom(s)? Could a lesion of the temporal lobes cause
visual field deficits? On slide 64, find the optic nerves and globes of the eyes. On
slide 65, find the optic tracts.
ANIMATION
Visual pathway
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DIENCEPHALON
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Describe the gross and macroscopic anatomy of the hypothalamus.
2. Define the major functions of the hypothalamus.
___________________________________________________________________
The hypothalamus is a subdivision of the diencephalon (L., interbrain). Other
subdivisions of the diencephalon are listed below:
A. Epithalamus -- consists of habenular nuclei and pineal gland.
B. Subthalamus -- previously studied with the basal ganglia.
C. Thalamus -- the thalamus is, by far, the largest component of the diencephalon.
We have studied the various nuclei of the thalamus and its relationship to
surrounding structures but will not have a separate laboratory on the thalamus.
However, it would serve you well to consider the following: The two thalami lie
interposed between 1) the cerebral cortex, 2) basal ganglia, 3) brain stem
centers, and 4) spinal cord. Consequently, each thalamus is intimately
associated with: 1) the sensory systems, by processing and relaying sensory
information to the cerebral cortex, 2) the motor systems, particularly with the
motor cortex, cerebellum and basal ganglia and 3) the limbic system, which
controls emotion, motivation, learning & memory and sexual behavior.
Moreover, the thalamus has reciprocal connections with virtually all areas of the
cerebral cortex.
D. HYPOTHALAMUS
Physically, the hypothalamus is a relatively small part of the diencephalon.
However, its small size is not an indicator of the importance of this structure.
From a functional standpoint, the hypothalamus is a central figure in the
regulation of a broad range of bodily functions. Through its endocrine
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connections via the pituitary gland, and its widespread nerve fiber connections
with a wide variety of other brain regions and spinal cord, it regulates endocrine,
autonomic, emotional and somatic activity.
1. Endocrine system
A. Direct regulation occurs through the hypothalamic-hypophyseal tract
(contains axons from the supraoptic and paraventricular nuclei of the
hypothalamus) which releases hormones (oxytocin and vasopressin) into
the capillaries of the general systemic circulation within the posterior
lobe of the pituitary.
B. Indirect regulation occurs through the tuberohypophyseal tract, which
delivers "releasing" and "inhibiting" factors to sinusoids in the
infundibulum. These factors then gain access to the anterior lobe via the
blood vessels of the hypophyseal portal system where they stimulate or
inhibit the release of a variety of hormones, such as prolactin, ACTH, LH
and others, into the systemic circulation.
2. Autonomic nervous system
A. The hypothalamus is involved in the expression of both parasympathetic
and sympathetic functions. Hence, it is often referred to as the "head
ganglion of the autonomic nervous system". Consequently, the
hypothalamus regulates basic physiologic functions such as temperature
regulation, heart rate, blood pressure and gastrointestinal activity. In
addition, through its connections with the limbic system, the
hypothalamus regulates emotion-based behavior such as anger, rage and
sexual activity. To produce these global effects, the hypothalamus has
extensive influence via the endocrine system and through synaptic
connections within the CNS.
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Whole and Half Brains
On the ventral surface of your whole brain specimens, find the optic nerves (CN II).
Gently elevate them and attempt to see the lamina terminalis, which forms both
the rostral wall of the 3rd ventricle and the rostral boundary of the hypothalamus.
Immediately caudal to the optic chiasm, the infundibulum can be seen. This
structure connects the hypothalamus with the pituitary (hypophysis). The region
of the hypothalamus between the infundibulum and the mammillary bodies is the
tuber cinereum. The rounded swellings of the mammillary bodies form the
caudalmost extent of the hypothalamus and reveal the location of the underlying
mammillary nuclei.
On the medial surface of your half brain specimens, find the lamina terminalis,
optic chiasm, tuber cinereum and mammillary body. The midline region
immediately dorsal to the optic chiasm, tuber cinereum and mammillary body is
the 3rd ventricle. The wall of the 3rd ventricle from this level dorsally to the
hypothalamic sulcus is formed by the hypothalamus. Note how the optic chiasm
fuses with the ventral portion of the hypothalamus. It is at this point that axons
from the ganglion cells of the retina enter the hypothalamus to provide regulation
of diurnal rhythms.
Slide Set
Begin with slide 24 and slide 25, which reveal the mammillary bodies in horizontal
sections of the hypothalamus. Slide 29, slide 30 and slide 31 also show the
mammillary bodies. Slide 32 is an oblique section in which the hypothalamus is
flanked laterally by the optic tracts. The 3rd ventricle can be seen in the midline.
Note the hypothalamic sulcus delineating the dorsal extent of the hypothalamus.
The large, compact fascicle of axons within the tuberal region is the fornix. This
important pathway to the hypothalamus will be discussed as part of the limbic
system. Slide 33 is an oblique section through the infundibulum protruding from
the ventral surface of the hypothalamus. On slide 33, identify the 3rd ventricle,
fornix and optic tracts.
Slide 38 is a relatively high power view of a coronal section through the anterior
commissure and rostral extent of the hypothalamus. Unlike all other brain
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sections in your slide set, this region is stained with a cellular stain. As such, the
nuclei (cell bodies) will stain darkly with the fiber tracts appearing unstained. Find
the 3rd ventricle. The rounded dark areas within the walls of the 3rd ventricle are
the paraventricular nuclei. The dorsal aspect of the optic chiasm can be seen as it
fuses with the hypothalamus ventrally. The darkly stained region in the lateral
concavity between the optic chiasm and the hypothalamus on each side are the
supraoptic nuclei. What neurotransmitter(s) is (are) secreted by the cells of the
paraventricular and supraoptic nuclei?
NEURORADIOLOGY
On slide 45, the hypothalamus can be seen ventral to the hypothalamic sulcus.
The mammillary bodies and infundibulum can also be seen. On slide 65, find the
mammillary bodies, hypothalamus and third ventricle.
ANIMATION
Diencephalon
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THE LIMBIC SYSTEM
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Identify the cortical and subcortical structures that make up the limbic system, including salient structures comprising “Papez Circuit.”
2. Relate the anatomical substrates of the limbic system to function.
___________________________________________________________________
The limbic system is that part of the brain controlling emotion, motivation, learning
and memory, and sexual behavior. It is composed of a series of cortical and
subcortical structures connected by fiber systems that join these cortical and
subcortical structures together to form "closed loop" circuits. Papez Circuit is the
most important example of a closed loop circuit and consists of the following
connections between limbic structures: hippocampal formation → via fornix →
mammillary bodies → via mammillothalamic tract → anterior nuclear group of the
thalamus → via anterior limb of internal capsule → cingulate cortex → via cingulum
→ parahippocampal (entorhinal) cortex → perforant pathway → hippocampal
formation. However, many of the structures in this and other loops either receive
afferents from other areas of the brain and/or project efferent axons to other
structures outside these so called "closed loop" circuits. This enables the limbic
system to influence a wide range of behaviors based on a variety of sensory inputs.
In addition to Papez Circuit, other critical structures and pathways in the limbic
system include the amygdala, which has connections with the hippocampal
formation, hypothalamus, thalamus and septal nuclei.
Half brain; Coronal and Horizontal Sections
Cortical components -- Turn your half brain specimens to observe the medial
surface. Immediately rostral to the anterior commissure and lamina terminalis is a
small vertical strip of cortex called the paraterminal gyrus. Just rostral to the
paraterminal gyrus and immediately ventral to the rostrum of the corpus callosum
is the subcallosal gyrus. These two gyri together are often referred to as the septal
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area. Follow the subcallosal gyrus rostrally to the genu of the corpus callosum
where the subcallosal gyrus becomes the cingulate gyrus. The cingulate gyrus
extends along the dorsal surface of the corpus callosum from the genu to the
splenium. Just caudal to the splenium of the corpus callosum the cingulate gyrus
narrows and dives ventrolaterally as the isthmus of the cingulate gyrus. The latter
is continuous with the parahippocampal gyrus on the ventromedial surface of the
temporal lobe. Due to an involution of the temporal cortex, the hippocampal
formation is hidden from view within the depths of the temporal lobe just caudal
to the uncus. This region of cortex is best seen on a coronal section.
Select a coronal section immediately caudal to the uncus. Just lateral (deep) to the
medial surface of the temporal lobe is an undulating region of cortex buried within
the temporal lobe. This is the hippocampal formation. In more caudal coronal
sections of the hippocampal formation, this structure has the appearance of a sea
horse from which it derives its name (G. hippokampos = sea horse). It is covered
ventrally by the parahippocampal gyrus. The region where the medial lip of the
parahippocampal gyrus bends 180o to turn dorsally and laterally is called the
subiculum, a component part of the hippocampal formation. The paraterminal
gyrus, subcallosal gyrus, cingulate gyrus, isthmus of the cingulate gyrus,
parahippocampal gyrus and hippocampal formation form a continuous cortical
circle or rim called the limbic lobe.
Subcortical nuclear components -- Select a coronal section that includes the uncus.
Deep (lateral) to the uncus within the temporal lobe is the rounded subcortical
nuclear mass of the amygdala. What sensory pathway has direct connections with
the amygdala? Note the close proximity of the amygdala and the hippocampal
formation.
Turn again to the medial surface of your half brain specimens. Deep (lateral) to the
septal area and immediately rostral to the anterior commissure are the septal
nuclei (these will be seen on slides). As previously mentioned, the hypothalamus
is a central figure in the limbic system.
Pathways connecting cortical and subcortical components of the limbic system -
On the medial surface of the half brain, find the body of the fornix as it arches from
caudal to rostral along the ventral border of the septum pellucidum. The fornix is
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the major efferent pathway from the hippocampus. As the fornix approaches the
rostral pole of the thalamus, it dives ventrally as the columns of the fornix (see Fig.
7 below).
The majority of axons in the columns of the fornix pass posterior to the anterior
commissure and penetrate the hypothalamus where they synapse in the
mammillary bodies. Those fibers of the fornix passing rostral to the anterior
commissure terminate primarily in the septal nuclei.
As the fornix arises from the hippocampus, it arches caudally and dorsally toward
the splenium of the corpus callosum. This can be seen in both horizontal and
coronal sections. Select a coronal section immediately caudal to the uncus and a
horizontal section looking down on the dorsal aspect of the thalamus just ventral
to the body of the corpus callosum. On the coronal section, note the thin strip of
white matter that forms the lateral wall of the hippocampal formation. This is the
alveus and is formed by the efferent fibers arising from the hippocampus. The
alveus courses dorsomedially to form a free lip of white matter called the fimbria,
the initial portion of the fornix. Select a more caudal coronal section through the
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splenium of the corpus callosum (if possible) and observe the fimbriae as they arch
dorsomedially to form the crura (sing. = crus) of the fornix.
At this time, try to find the crura, body and columns of the fornix on the horizontal
sections. NOTE: If you cannot find the above structures on your sections due to the
"luck of the cut", look on your neighbor's specimens and/or look at the
demonstrations.
Now follow the body of the fornix rostrally on your coronal sections. Note the
relationship between the columns of the fornix and the anterior commissure. In a
section containing the anterior thalamic nuclei and/or the mammillary bodies, you
may be able to find the columns of the fornix as they dive ventrally within the
substance of the hypothalamus to terminate in the mammillary bodies. Find the
cingulate gyrus on your coronal sections. The white matter immediately deep to
the gray matter of the cingulate cortex is the cingulum, which contains the efferent
axons from the cingulate gyrus to the parahippocampal gyrus.
Slide Set
The following slides (26-36,38,39) will reveal cortical regions and subcortical nuclei
as well as pathways of the limbic system. As you proceed through these slides,
attempt to correlate them with the wet brain specimens.
Begin with slide 26. Immediately dorsal to the pulvinar on both sides lie the crura
of the fornix. Sandwiched between the crura is the caudal extent of the body of
the corpus callosum. Just lateral to the fornix lies the body of the caudate nucleus.
The lower left side of this slide reveals a coronal section through the temporal lobe
at the level of the hippocampal formation. The cortical region medially and
ventrally is the parahippocampal gyrus.
A higher power view of the hippocampal formation, which is composed of the
hippocampus proper, dentate gyrus and subiculum, can be seen on slide 27. The
gray matter on the dorsal region of the parahippocampal gyrus where it swerves
laterally (i.e., toward left side) is called the subiculum. The hippocampus proper
extends from where the subiculum meets the overlying dentate gyrus. The groove
between the hippocampus proper and overlying dentate gyrus is called the
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hippocampal fissure. Note that the hippocampus proper extends laterally from the
hippocampal fissure and arches dorsally to terminate by tucking its "head" into the
dentate gyrus. The darkly stained white matter dorsal to the dentate gyrus is the
fimbria of the fornix, which tapers laterally as the alveus. Identify the choroid
plexus extending laterally from the fimbria of the fornix. The space medial to the
choroid plexus is the subarachnoid space, whereas the space lateral to the choroid
plexus is the inferior (temporal) horn of the lateral ventricle.
Slide 28 is slightly more rostral. Find the fornix, hippocampal formation and
inferior horn of the lateral ventricle.
Slide 30 illustrates the origin of the mammillothalamic tract as it arises from the
medial aspect of the mammillary nuclei. Where does this fiber tract terminate?
Also note the lightly stained uncus of the temporal lobes located ventrolateral to
the mammillary bodies. The region deep (lateral) to the uncus is the amygdala.
Slide 31 shows the body and columns of the fornix, mammillothalamic tract,
uncus and amygdala.
Slide 32 and slide 33 illustrate the body and columns of the fornix. On slide 33, the
mammillothalamic tract is visible on the right side as a looping fascicle of axons
approaching the anterior nuclear group from the ventral side.
Slide 36 is a horizontal section through the thalamus. The septal nuclei can be seen
just rostral to the columns of the fornix.
Slide 38 is a cellular stain of a coronal section through the anterior commissure.
Find the columns of the fornix and the septal nuclei.
Slide 39 is a sagittal section of the brainstem. Is this a midsagittal section? Can you
defend your answer based on sound anatomical evidence? Find the body and
columns of the fornix, anterior commissure, mammillary body, and
mammillothalamic tract.
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NEURORADIOLOGY
On slide 45, find the paraterminal gyrus, cingulate gyrus, and the fornix. What
region on this slide represents the septal area? Slide 46 shows the hippocampal
formation. Slide 48 and slide 49 illustrate the columns of the fornix.
ANIMATIONS
Limbic structures (parts, zoom).
Hippocampus, hippocampus-septal nuclei, amygdala-hippocampus.
DEMONSTRATIONS
Whole brain (ventral view) showing: Hippocampal Formation, Fornix.
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CEREBRAL CORTEX AND REVIEW
Learning Objectives:
At the end of the laboratory session students will be able to:
1. Revisit those areas of primary cortex previously learned and review their location and function.
2. Recognize other areas of cortex presented in this lab with particular emphasis on those areas related to speech.
3. List the clinical symptoms related to lesions of cortical areas as presented in lecture.
4. Review and describe the blood supply to all cortical areas.
5. Review and describe the major Brodmann Areas as presented in lecture.
6. Review and describe the sensory and motor homunculi as presented in lecture.
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The advanced development of the cerebral cortex in humans gives us our unique
abilities to participate in language and abstract thinking. The cerebral cortex is also
critically involved in our perception of the outside world and our ability to move
and adapt to our environment.
Based on phylogenetic relationships and differences in cytoarchitecture, there are
three types of cerebral cortex: neocortex, paleocortex and archicortex (i.e.,
hippocampal formation). Neocortex comprises the vast majority of the cerebral
cortex (over 90%) and as the name implies, it is the most recent type of cortex to
develop.
Through the years, a number of anatomists have attempted to categorize the
cerebral cortex based on neural cytoarchitecture and relate these anatomical
differences to the function of specific cortical areas. Overall, Brodmann's (circa
1909) numerical classifications of 52 cortical regions have emerged as the standard
and have generally withstood the test of time. However, as more information is
gathered on brain function using more sophisticated research techniques, our
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understanding of the functioning of the various regions of the cerebral cortex, and
the CNS as a whole, is rapidly evolving.
To ease your fears, we will only focus on a few of Brodmann's 52 areas of the
cerebral cortex that relate to a specific modality or function (Fig. 8). Some of this
laboratory session will be a review of cortical areas we have already studied. For
example, Brodmann's area 4 of the precentral gyrus contributes axons to the
corticospinal and corticobulbar pathways. You should be able to identify the
location of these pathways on both your wet brain specimens and your slide sets.
You should perform this exercise on all known ascending and descending pathways.
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Whole and Half Brains
On the left lateral surface of the cerebral cortex, identify the central sulcus,
precentral gyrus, and the superior, middle and inferior frontal gyri. Make sure
you understand the somatotopic arrangement of the precentral gyrus. Identify the
general region of the premotor area (area 6) and frontal eye fields (area 8). An
ablative lesion of area 8 on the left side results in what symptom(s)? Find the
Sylvian fissure. The inferior frontal gyrus lies on the superior bank of this fissure
just rostral to the precentral gyrus and is divided into three parts from caudal to
rostral. The opercular part of the inferior frontal gyrus is small and lies just rostral
to the precentral gyrus; the triangular part resembles an inverted triangle. Both
the opercular and triangular portion represent Broca's speech area (areas 44,45).
Lesion of this area results in Broca's aphasia. What are the symptoms of Broca's
aphasia? What region of the body is controlled by the precentral gyrus immediately
caudal to Broca's area? If the Sylvian fissure is gently opened, the insular cortex
can be seen. Can you name two sensory modalities that terminate in the insular
cortex?
On a lateral view of the left temporal lobe, find the superior, middle and inferior
temporal gyri. The dorsal surface of the superior temporal gyrus is hidden by the
frontal and parietal opercula, and contains the transverse gyri of Heschl (areas
41,42). What symptom(s) would you expect to observe if Heschl's gyri were lesioned
on the left side? The lateral surface of the superior temporal gyrus, approximately
from the level of the precentral gyrus rostrally to the posterior portion of the
supramarginal gyrus caudally, contains the auditory association area (area 22).
The posterior portion of area 22 is Wernicke's area, which acts to integrate visual
and auditory information required to comprehend written and spoken language. A
lesion of this area results in Wernicke's aphasia. Can you describe the symptoms
of Wernicke's aphasia?
Immediately caudal to the supramarginal gyrus of the parietal lobe is the angular
gyrus. These two gyri form the inferior parietal lobule. A lesion of the inferior
parietal lobule, but not Wernicke's area, results in a complex series of disorders
which may include any combination of the following: alexia, anomia,
constructional apraxia, agraphia, finger agnosia and confusion or inability to
distinguish between the left and right sides of the body. Can you define the above
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terms that describe this lesion? What symptoms would you expect to see in a
comparable lesion of the right cerebral hemisphere? What artery supplies this
region? Find the postcentral gyrus (areas 3,1,2). This is the somatosensory cortex.
What pathways terminate along this somatotopically arranged gyrus?
Find the calcarine fissure at the caudal pole of the occipital lobe. The gyri forming
the upper and lower lips of this fissure are the primary visual cortex (area 17). The
visual association areas (areas 18 and 19), are arranged concentrically around area
17 on the lateral surface of the occipital lobe. Now follow the calcarine fissure
around to the medial surface of the occipital lobe, where this fissure forms a deep
horizontal groove that projects laterally. Thus, although area 17 can be seen
immediately dorsal (cuneus) and ventral (lingula) to the calcarine fissure, much of
area 17 is hidden from view within the depths of the occipital lobe. As on the lateral
surface of the occipital lobe, areas 18 and 19 surround area 17. What symptoms
would result following a lesion of the left primary visual cortex? What major artery
supplies this region? Follow the calcarine fissure rostrally where it is joined by the
parietooccipital sulcus. Find the cingulate gyrus, the isthmus of the cingulate
gyrus and the paracentral lobule. What Brodmann's areas are encompassed by the
paracentral lobule? What part(s) of the body does the paracentral lobule serve? Is
the paracentral lobule sensory or motor? What symptoms would you see if it were
lesioned? What artery supplies the paracentral lobule? Follow the cingulate gyrus
as it curves ventrally around the genu of the corpus callosum to become the
subcallosal gyrus. Also identify the paraterminal gyrus. What diencephalic nucleus
projects to the cingulate gyrus? To what important system does the cingulate gyrus
belong?
Turn to the ventral surface of the brain and identify the uncus and
parahippocampal gyrus. What important structure lies deep to the uncus? What
clinical symptoms would you see if this structure was lesioned bilaterally? What is
the classification of cerebral cortex that comprises the uncus?
The remaining areas of cortex come under the broad heading of association
cortices, which correlate the various sensory inputs and deliver them to the
appropriate cortical areas for action.
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Intercortical Connections -- Afferent input to the cerebral cortex comes from a
variety of subcortical structures. However, the thalamus, via the internal capsule,
provides the greatest single source of subcortical input to the cerebral cortex.
Similarly, efferents from the cerebral cortex also pass to subcortical structures
primarily through the internal capsule.
With the possible exception of the visual cortex, virtually all areas of the cerebral
cortex interconnect across the midline with comparable cortical areas via
subcortical white matter called commissural fibers (pathways). Ipsilateral
connections (within the same hemisphere) are accomplished by way of association
fibers.
Commissural fibers -- Turn to the medial surface of your half brain sections.
Identify the rostrum, genu, body and splenium of the corpus callosum. It is this
massive interhemispheric commissure that provides the vast majority of
commissural fibers between the cerebral hemispheres. The anterior commissure
also transmits interhemispheric fibers between the temporal lobes. Why isn't the
posterior commissure included in this group of commissural fibers?
Association fibers -- The general location of
association fiber bundles can be determined using
a coronal section midway through the body of the
corpus callosum. Identify the location of the
following fiber bundles within the white matter
deep to the cellular layers of the cerebral cortex.
The white matter immediately deep (lateral) to the
cingulate cortex is the cingulum, which connects
the cingulate cortex with the parahippocampal
gyrus and hippocampal formation. Just dorsal to
the insular cortex lies the superior longitudinal
(arcuate) fasciculus, which interconnects
ipsilateral frontal, parietal, occipital and temporal
lobes. It is the arcuate fasciculus that interconnects Wernicke's and Broca's areas.
A lesion of the arcuate fasciculus deep to the parietal operculum produces
conduction aphasia. What are the symptoms of conduction aphasia?
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Cerebral Dominance -- In our study of the cerebral hemispheres thus far, they have
appeared separate, but equal. That is, there have been similar functions in similar
locations in both hemispheres, and each hemisphere primarily controls functions
of the contralateral side of the body. However, this concept cannot be applied to
the important function of language, which typically resides in one hemisphere only.
That hemisphere that controls language is generally agreed to be the dominant
hemisphere. In over 90% of humans, the dominant hemisphere is the left
hemisphere. The dominant hemisphere is also related to handedness, since 95%
of right-handed individuals are left hemisphere dominant. This number drops to
approximately 50% in left-handed individuals. It should be noted that a few
individuals possess language areas in both hemispheres. It should also be
remembered that the non-dominant (usually right) hemisphere should not be
viewed as less important, since it is the "dominant" hemisphere when it comes to
artistic talent, music and spatial perception.
DEMONSTRATIONS
Insula, Broca's area, Wernicke's area, Heschl's gyri
Brodmann's areas
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NEUROROUND CC: “Mom just isn’t herself any more.” HPI: Mrs. S. is a 61 y/o homemaker who is brought by her daughter for evaluation. The
daughter reports a three-month history of her mother “not being herself.” When pressed to amplify this, she suspects she is depressed, reporting symptoms of apathy, being rather listless and drowsy at times and just not caring about what is going on around her. Her appetite remains good and she sleeps well. She reports this is in stark contrast to her mom’s usual behavior, which has often been described as “the life of the party.” The entire family is concerned about what they perceive as a dramatic change in their mother.
The patient reports increasing headaches, worse at night and upon waking. These have occurred for the last six months or so but are generally relieved by taking 800 mg of Ibuprofen four times a day. She has a history of migraine headaches but for which she takes Bellergal tablets and an occasional injection of Imatrex. These medications do not seem to prevent these recent headaches which seem different than her migraines. She also reports occasional dizziness but denies any sensation of the room itself moving. When questioned about what she feels is going on, she simply says her family just can’t cope with the fact that she “getting to be an old woman.” Finally, she reports two or three occasions of nausea and vomiting recently, once with some slight hematemesis.
After stepping out of the room so the patient could change for the physical exam, the daughter comes out and tells you that four weeks ago they found her mom incontinent and unconscious on the bathroom floor. She quickly “came to” and after a 20 minute period of being confused, refused to go to the doctor. She said she just slipped and hit her head.
PE: 62 y/o female in no apparent distress, appearing a bit older than stated age:
VS: BP 148/100; P - 73 (irregular); R – 15; T - 98.7
HEENT: Extraocular movements intact. Pupils equally round and reactive to light. Funduscopic exam shows papilledema, worse on the right. Nose - clear.
Throat: non-erythematous.
Neck: Supple with no adenopathy
Chest: Lungs clear. Heart rate is normal but “irregularly irregular.”
Abd: Non-distended. Mild pain to palpation in the epigastric region. No organomegaly or bruits.
Pelvic: s/p hysterectomy with no masses palpated. Rectal exam showed no masses but stool was guaiac positive.
MSK: Normal range of motion of limbs. See neuro exam below.
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Neuro Exam:
Mood and affect: patient seems rather apathetic; answers questions quite slowly with long pauses between question and her answer,how-ever, her answers are appropriate and more detailed than expected given her general stupor.
CN’s II–XII: intact.
Muscle strength: 2+ bilaterally except 1+ in left arm (biceps, triceps).
DTR’s: (R/L & 2+ is normal) – biceps: 2+/3+ triceps: 2+/3+ knee: 2+/3+ ankle: 1+/3+
Clonus was elicited in the left ankle.
Plantar reflexes: down-going on the right; up-going on the left.
Gait: slight limp on the left, no ataxia.
Other: no dysdiadochokinesia, dysmetria, nystagmus. LAB: CBC – normal Chest x-ray – mild cardiomegaly, clear lungs. Electrolytes – normal. Barium enema – sigmoid diverticulosis. Upper GI – 2 cm ulcer along the greater curvature of the stomach. MRI of brain – abnormal, results pending. In your diagnosis of this case, answer the following: 1. What about this patient’s history and physical lead you away from a diagnosis of
depression?
2. What do you think had occurred when the patient was found unconscious?
3. What combination of symptoms is ominous?
4. What is the first sign listed in the physical exam that suggests that a tumor might be the cause for this patient’s problems? Assuming this is not a case of metastatic disease, what is the most likely diagnosis and location of the tumor?
5. Which signs suggest an upper motor neuron lesion?
6. What are possible causes for the vomiting? Hematemesis?
7. What does the “irregularly irregular” heart rate suggest and how might it cause neurological symptoms?
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NEUROROUND
A 45 y/o construction worker was hit in the head by a steel beam. Co-workers at the job site ran to his aid and reported that he was unarousable for about 60 seconds then slowly regained consciousness. Over the next 5 minutes or so he was confused about where he was but otherwise could answer appropriately. The EMS was called and transported him to the local Podunk Heights Emergency Room within 15 minutes of his injury. Upon arrival at the E.R., his vitals signs were normal, including a BP of 133/83. He was alert and oriented time 3, though perhaps slightly confused about why he was at the hospital. Other than reporting a headache, he claimed to feel normal. Physical exam showed a 4 cm scalp laceration over the left temple. Neurological exam showed CN’s II-XII to be intact. There was no muscle weakness. A skull radiograph was reported as normal. His laceration was sutured and he was discharged to home with a prescription for Tylenol #3 as needed for pain. Three hours later his wife noted that he started to get nauseated and vomited twice. There was no hematemesis. In talking with him, she felt he seemed to be a bit more confused, although he still was able to answer all questions. She decided to take him back to the E.R. for a recheck. Upon arrival at the E.R., now six hours post-injury, his vital signs were again normal. His pupils were equally round and reactive to light and extraocular movements were intact. No neurological abnormalities were found. He was diagnosed as having a post-concussion syndrome and admitted overnight for observation. Upon arrival at the hospital floor, the nurse checking him in felt he was somewhat lethargic, though arousable. The E.R. physician came up to re-examine him and found some questionable weakness on his right side. A questionable Babinski sign was elicited on the right. Given his questionably changing neurological status, a CT scan of the brain was ordered. The scan showed a lens-shaped collection of blood beneath the left fronto-temporal region with slight shift of the frontal horns of the lateral ventricles to the right. A neurosurgeon was called. His examination of the patient showed the following: eyes open only in response to pain, left pupil dilated and unresponsive/right pupil minimally dilated and sluggish in response to light, funduscopic exam normal, patient muttering inappropriate words. His breathing became slightly erratic at this point. He also began to show some decorticate posturing and bilateral Babinski signs. His BP found to be 169/82. The patient was intubated and hyper-ventilated. Some IV Mannitol was started then he was taken to the O.R. for an operative procedure.
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In your diagnosis of this case, answer the following: 1. How was this patient’s presentation typical for the problem he has?
2. Discuss the ramifications of the normal skull radiograph, how it helps or hurts making a diagnosis.
3. How do these symptoms differ from a post-concussion syndrome?
4. What is the significance of the right-sided Babinski? Why did it later become bilateral?
5. Explain the changing responses of the pupils reacting to light.
6. Estimate his Glasgow Coma scale rating preoperatively.
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Labeled Atlas of Representative Sections of Spinal Cord and Brain from your Slide Set
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