bio 130 chapter 12 notes

10
Nervous System: Nervous Tissue (Chapter 12) Lecture Materials for Amy Warenda Czura, Ph.D. Suffolk County Community College Eastern Campus Primary Sources for figures and content: Marieb, E. N. Human Anatomy & Physiology 6th ed. San Francisco: Pearson Benjamin Cummings, 2004. Martini, F. H. Fundamentals of Anatomy & Physiology 6th ed. San Francisco: Pearson Benjamin Cummings, 2004. Neural Tissue -3% of body mass -cellular, ~20% extracellular space -two categories of cells: 1. Neurons: conduct nervous impulses 2. Neuroglia / glial cells: “nerve glue”, supporting cells Organization of Nervous System 1. Central Nervous System (CNS) -spinal cord, brain -function: integrate, process, coordinate sensory input and motor output 2. Peripheral Nervous System (PNS) -all neural tissue outside CNS -function: carry info to/from CNS via nerves Nerve = bundle of axons (nerve fibers) with blood vessels and CT -cranial nerves " brain -spinal nerves " spinal cord Divisions of PNS: 1. Sensory/Afferent Division -sensory receptors ! CNS A. Somatic afferent division -from skin, skeletal muscles, joints B. Visceral afferent division -from internal organs 2. Motor/Efferent Division -CNS ! effectors A. Somatic Nervous System -“voluntary nervous system” -to skeletal muscles B. Autonomic Nervous System (ANS) -“involuntary nervous system” -to smooth & cardiac muscle, glands 1. Sympathetic Division - “fight or flight” 2. Parasympathetic Division - “rest and digest” (tend to be antagonistic to each other) Histology of Nervous System Neuron / Nerve cell -function:conduct nervous impulses (message) -characteristics: 1. Extreme longevity 2. Amitotic (exceptions: hippocampus, olfactory receptors) 3. High metabolic rate: need O 2 and glucose Amy Warenda Czura, Ph.D. 1 SCCC BIO130 Chapter 12 Lecture Notes

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  • Nervous System: Nervous Tissue

    (Chapter 12)

    Lecture Materials

    for

    Amy Warenda Czura, Ph.D.

    Suffolk County Community College

    Eastern Campus

    Primary Sources for figures and content:

    Marieb, E. N. Human Anatomy & Physiology 6th ed. San Francisco: Pearson Benjamin

    Cummings, 2004.

    Martini, F. H. Fundamentals of Anatomy & Physiology 6th ed. San Francisco: Pearson

    Benjamin Cummings, 2004.

    Neural Tissue

    -3% of body mass

    -cellular, ~20% extracellular space

    -two categories of cells:

    1. Neurons: conduct nervous impulses

    2. Neuroglia / glial cells: nerve glue,

    supporting cells

    Organization of Nervous System

    1. Central Nervous System (CNS)

    -spinal cord, brain

    -function: integrate, process, coordinate

    sensory input and motor output

    2. Peripheral Nervous System (PNS)

    -all neural tissue outside CNS

    -function: carry info to/from CNS via nerves

    Nerve = bundle of axons (nerve fibers) with

    blood vessels and CT

    -cranial nerves " brain

    -spinal nerves " spinal cord

    Divisions of PNS:

    1. Sensory/Afferent Division

    -sensory receptors ! CNS

    A. Somatic afferent division

    -from skin, skeletal muscles, joints

    B. Visceral afferent division

    -from internal organs

    2. Motor/Efferent Division

    -CNS ! effectors

    A. Somatic Nervous System

    -voluntary nervous system

    -to skeletal muscles

    B. Autonomic Nervous System (ANS)

    -involuntary nervous system

    -to smooth & cardiac muscle, glands

    1. Sympathetic Division

    - fight or flight

    2. Parasympathetic Division

    - rest and digest

    (tend to be antagonistic to each other)

    Histology of Nervous System

    Neuron / Nerve cell

    -function:conduct nervous impulses (message)

    -characteristics:

    1. Extreme longevity

    2. Amitotic (exceptions: hippocampus,

    olfactory receptors)

    3. High metabolic rate: need O2 and glucose

    Amy Warenda Czura, Ph.D. 1 SCCC BIO130 Chapter 12 Lecture Notes

  • Structure:

    -large soma / perikaryon

    -large nucleus, large nucleolus (rRNA)

    -many mitochondria, ribosomes, RER, Golgi:

    (#ATP, #protein synthesis to produce

    neurotransmitters)

    -Nissl bodies: visible RER & ribosomes, gray

    -neurofilaments = neurofibrils, neurotubules

    (internal structure)

    -no centrioles

    -2 types of

    processes:

    (cell extensions)

    1. Dendrites:

    -receive info

    -carry a graded potential toward soma

    -contain same organelles as soma

    -short, branched

    -end in dendritic spines

    2. Axon:

    -single, long

    -carry an action potential away from soma

    -release neurotransmitters at end to signal

    next cell

    -long ones = nerve fibers

    -contains:

    -neurofibrils & neurotubules (abundant)

    -vesicles of neurotransmitter

    -lysosomes, mitochondria, enzymes

    -no Nissl bodies, no Golgi (no protein

    synthesis in axon)

    -connects to soma at axon hillock

    -covered in axolemma (membrane)

    -may branch: axon collaterals

    -end in synaptic terminals or knobs

    -may have myelin sheath: protein+lipid

    -protection

    -insulation

    -increase speed of impulse

    CNS: myelin from oligodendrocytes

    PNS: myelin from Schwann cells

    Axoplasmic transport

    -move materials between soma and terminal

    -along neurotubules on kinesins

    -Anterograde transport = soma ! terminal

    (neurotransmitters from soma)

    -Retrograde transport = terminal ! soma

    (recycle breakdown products from used

    neurotransmitters)

    Some viruses use retrograde transport to

    gain access to CNS (Polio, Herpes,

    Rabies)

    Amy Warenda Czura, Ph.D. 2 SCCC BIO130 Chapter 12 Lecture Notes

  • -presynaptic cell sends message along axon to

    axon terminal

    -postsynaptic cell receives message as

    neurotransmitter

    Neurotransmitter = chemical, transmits signal

    from pre- to post- synaptic cell across

    synaptic cleft

    Synaptic knob = small, round, when

    postsynaptic cell is neuron, synapse on

    dendrite or soma

    Synaptic terminal = complex structure, at

    neuromuscular or neuroglandular junction

    Synapse

    -site where neuron

    communicates with

    another cell:

    neuron or effector

    Structural classification of neurons:

    1. Anaxonic neurons:

    -dendrites and axon look same

    -brain and special sense organs

    2. Bipolar neurons:

    -1 dendrite, 1 axon

    -soma in middle

    -rare: special sense organs,

    relay from receptor to neuron

    3. Unipolar neurons:

    -1 long axon, dendrites at one

    end, soma off side (T shape)

    -most sensory neurons

    4. Multipolar neurons:

    -2 or more dendrites

    -1 long axon

    -99% all neurons

    -most CNS

    Functional Classification of Neurons:

    1. Sensory/Afferent neurons

    -transmit info from sensory receptors to CNS

    -most unipolar

    -soma in peripheral sensory ganglia

    Ganglia = collection of cell bodies in PNS

    A. Somatic sensory neurons

    -receptors monitor outside conditions

    B. Visceral sensory neurons

    -receptors monitor internal conditions

    2. Motor/Efferent neurons

    -transmit commands from CNS to effectors

    -most multipolar

    A. Somatic motor neurons

    -innervate skeletal muscle

    -conscious control or reflexes

    B. Visceral/Autonomic motor neurons

    -innervate effectors on smooth muscle,

    cardiac muscle, glands, adipose

    3. Interneurons / Association neurons

    -distribute sensory info and coordinate motor

    activity

    -between sensory and motor neurons

    -in brain, spinal cord, autonomic ganglia

    -most are multipolar

    Neuroglia =supporting cells

    Neuroglia in CNS

    -outnumber neurons 10:1

    -half mass of brain

    Amy Warenda Czura, Ph.D. 3 SCCC BIO130 Chapter 12 Lecture Notes

  • 1. Ependymal cells

    -line central canal of spinal

    cord and ventricles of brain

    -secrete cerebrospinal fluid

    (CSF)

    -have cilia to circulate CSF

    -CSF: cushion brain, nutrient & gas exchange

    2. Astrocytes

    -most abundant CNS

    neuroglia

    -varying functions:

    a. blood brain barrier:

    processes wrap capillaries, control

    chemical exchange between blood and

    interstitial fluid of brain

    b. framework of CNS

    c. repair damaged neural tissue

    d. guide neuron development in embryo

    e. control interstitial environment: regulate

    conc. ions, gasses, nutrients, neurotransmitters

    3. Oligodendrocytes

    -wide flat processes wrap

    local axons = myelin

    sheath

    -1 cell contributes myelin to many

    neighboring axons

    -lipid in membrane insulates axon for faster

    action potential conductance

    -gaps on axon between processes/myelin =

    Nodes of Ranvier, necessary to conduct

    impulse

    -white, myelinated axons = white matter

    4. Microglia

    -phagocytic

    -wander CNS

    -engulf debris, pathogens

    -important CNS defense

    (no immune cells or antibodies)

    Cells in the CNS Neuroglia in PNS

    1. Satellite cells

    -surround somas in ganglia

    -isolate PNS cells

    -regulate interstitial environment of ganglia

    2. Schwann cells

    -myelinate axons in PNS

    -whole cells wraps axon,

    many layers

    -Neurilemma: bulge of schwann cell,

    contains organelles

    -Nodes of Ranvier between cells

    Amy Warenda Czura, Ph.D. 4 SCCC BIO130 Chapter 12 Lecture Notes

  • -vital to repair of peripheral never fibers after

    injury: guide growth to original synapse

    -some hold bundles of unmyelinated axons

    + + + +

    +

    + + + ++

    + + + +

    ++

    +

    +

    + ++ + +

    ++

    ++

    -

    --- - -

    - -

    -- - - - ----

    - - - -

    Neurophysiology

    Neurons: conduct electrical impulse

    -requires transmembrane potential = electrical

    difference across cell membrane

    -cells: positive charge outside (pump cations

    out) and negative charge inside (proteins)

    Voltage = measure of potential energy

    generated by separation of opposite charges

    Current = flow of electrical charges (ions)

    Cell can produce current (nervous impulse)

    when ions move to eliminate the potential

    difference (volts) across the membrane

    Resistance = restricts ion movement (current)

    (high resistance = low current); membrane

    has resistance, restricts ion flow/current

    Ohms Law: current = voltage resistance

    Current highest when voltage high and

    resistance low

    Cell voltage set at -70mV but membrane

    resistance can be altered to create current

    Membrane resistance depends on permeability

    to ions: open or close ion channels

    Cell must always have some resistance or ions

    would equalize, voltage = zero,

    no current generated = no nervous impulse

    Membrane ion channels:

    -allow ion movement (alter resistance)

    -each channel specific to one ion type

    1. Passive channels (leak channels)

    -always open, free flow

    -sets resting membrane potential at -70mV

    2. Active channels

    -open/close in response to signal

    A. Chemically regulated/ Ligand-gated

    -open in response to chemical binding

    -located on any cell membrane

    (dendrites, soma)

    B. Voltage regulated channels

    -open/close in response to shift in

    transmembrane potential

    -excitable membrane only: conduct

    action potentials (axolemma,

    sarcolemma)

    Amy Warenda Czura, Ph.D. 5 SCCC BIO130 Chapter 12 Lecture Notes

  • C. Mechanically regulated channels

    -open in response to membrane

    distortion

    -on dendrites of sensory neurons for

    touch, pressure, vibration

    When channel opens, ions flow along

    electrochemical gradient:

    -diffusion (high conc. to low)

    -electrical attraction/repulsion

    Sodium-Potassium Pump:

    -uses ATP to move 3 Na+ out 2 K+ in

    (70% of neuron ATP for this)

    -runs anytime cell not conducting impulse

    -creates high [K+] inside and high [Na+]outside

    When Na+ channel opens:

    - Na+ flows into cell:

    1. Favored by diffusion gradient

    2. Favored by electrical gradient

    open channel = $resistance = #ion flow/current

    When K+ channel opens:

    - K+ flows out of cell:

    1. Favored by diffusion gradient only

    2. Electrical gradient repels K+ exit

    - Thus less current than Na+

    Channels open = resistance low = ions move

    until equilibrium potential: depends on

    -diffusion gradient

    -electrical gradient

    Equilibrium Potential

    For K+ = -90mV

    For Na+ = +66mV

    Open channel ! current ! graded potential

    Graded potential = localized shift in

    transmembrane potential due to

    movement of charges in to /out of cell

    Na+ channel opens = Na+ flows in,

    depolarization (cell less negative)

    K+ channel opens = K+ flows out,

    hyperpolarization (cell more negative)

    Graded potentials:

    -occur on any membrane: dendrites and somas

    -can be depolarizing or hyperpolarizing

    -amount of depolarization or hyperpolarization

    depends on intensity of stimulus:

    # channels open = # voltage change

    -passive spread from site of stimulation over

    short distance

    -effect on membrane potential decreases with

    distance from stimulation site

    -repolarization occurs as soon as stimulus is

    removed: leak channels & Na+/K+ pump

    reset resting potential

    Graded potential = localized change in

    transmembrane potential, not nervous

    impulse (message)

    Amy Warenda Czura, Ph.D. 6 SCCC BIO130 Chapter 12 Lecture Notes

  • If big enough depolarization = action potential

    = nervous impulse = transmission to

    next cell

    Action potentials:

    -occur on excitable membranes only

    (axolemma, sarcolemma)

    -always depolarizing

    -must depolarize to threshold (-55mV) before

    action potential begins

    (voltage gated channels on excitable

    membrane open at threshold to

    propagate action potential)

    - all-or-none : all stimuli that exceed

    threshold will produce identical action

    potentials

    -action potential at one site depolarizes

    adjacent sites to threshold

    -propagated across entire membrane surface

    without decrease in strength

    The Generation of

    an Action Potential

    -55 mV

    1. Depolarization to threshold:

    - a graded potential depolarizes local

    membrane and flows toward the axon

    - if threshold is met (-55mV) at the hillock, an

    action potential will be triggered

    2. Activation of sodium channels and rapid

    depolarization:

    - at threshold (-55mV), voltage-regulated

    sodium channels on the excitable

    membrane open

    - Na+ flows into the cell depolarizing it

    - the transmembrane potential rapidly changes

    from -55mV to +30mV

    3. Inactivation of sodium channels and

    activation of potassium channels:

    - at +30mV Na+ channels close and K+

    channels open

    - K+ flows out of the cell repolarizing it

    4. Return to normal permeability:

    - at -70mV K+ channels begin to close

    - the cell hyperpolarizes to -90mV until all

    channels finish closing

    - leak channels restore the resting membrane

    potential to -70mV

    (Handout)

    Restimulation only when Na+ channels closed:

    influx of Na+ necessary for action potential

    Absolute Refractory Period = -55mV

    (threshold) to +30mV, Na+ channels open,

    membrane cannot respond to additional

    stimulus

    Relative Refractory Period = +30mV to

    -70mV (return to resting potential), Na+

    channels closed, membrane capable of

    second action potential but requires

    larger/longer stimulus (threshold elevated)

    Cell has ions for thousands of action potentials

    Eventually must run Sodium-Potassium pump

    (burn ATP) to reset high [K+] inside and

    high [Na+] outside

    (Death = no ATP, but stored ions can

    generate action potentials for awhile)

    Propagation of Action Potentials

    -once generated must be transmitted length of

    axon: hillock to terminal

    -speed depends on:

    1. Degree of myelination

    2. Axon diameter

    1. Myelination

    A. Continuous Propagation:

    -unmyelinated axons

    -whole membrane depolarizes and

    repolarizes sequentially hillock to

    terminal

    -only forward movement; membrane

    behind always in absolute refractory

    period

    Amy Warenda Czura, Ph.D. 7 SCCC BIO130 Chapter 12 Lecture Notes

  • B. Saltatory propagation

    -myelinated axons

    -depolarization only on exposed

    membrane at nodes

    -myelin insulates covered membrane

    from ion flow

    -action potential jumps from node to

    node: faster and requires less

    energy to reset

    Continuous Propagation Saltatory Propagation

    2. Axon diameter

    -larger axon ! less resistance ! easier ion

    flow ! faster action potential

    A. Type A Fibers

    - 4-20m diameter

    - myelinated (saltatory propagation)

    - action potentials 140m/sec

    - carry somatic motor and somatic

    sensory info

    B. Type B Fibers

    - 2-4m diameter

    - myelinated (saltatory propagation)

    - action potentials 18m/sec

    - carry autonomic motor and visceral

    sensory info

    C. Type C Fibers

    - < 2m diameter

    - unmyelinated (continuous propagation)

    - action potentials 1m/sec

    - carry autonomic motor and visceral

    sensory info

    Myelination:

    -requires space, metabolically expensive

    -only important fibers large and myelinated

    -occurs in early childhood

    -results in improved coordination

    Multiple Sclerosis = genetic disorder, myelin

    on neurons in PNS destroyed !

    numbness, paralysis

    Synapse = junction between transmitting

    neuron (presynaptic cell) and receiving

    cell (postsynaptic cell), where nerve

    impulse moves from one cell to next

    Two types:

    1. Electrical Synapse

    -direct contact via gap junctions

    -ions flow directly from pre to post cell

    -less common synapse

    -in brain (conscious perception)

    2. Chemical synapse

    -most common

    Amy Warenda Czura, Ph.D. 8 SCCC BIO130 Chapter 12 Lecture Notes

  • -pre and post cells separated by synaptic cleft

    -presynaptic neuron releases neurotransmitter

    to trigger effect on post synaptic cell

    -dynamic: facilitate or inhibit transmission,

    depends on neurotransmitter:

    1. Excititory Neurotransmitters =

    -depolarization

    -propagate action potential

    2. Inhibitory Neurotransmitters =

    -hyperpolarization

    -suppress action potential

    Propagation across chemical synapse always

    slow but allows variability

    Events at a Synapse:

    e.g.Cholinergic Synapse(Acetylcholine as neurotransmitter)

    (Handout)

    Neurotransmitter Mechanism of Action

    1. Direct effect on membrane potential

    2. Indirect effect on membrane potential

    (Handout)

    (Handout)

    Post synaptic potential = graded potential

    caused by a neurotransmitter due to

    opening or closing of ion channels on

    post synaptic cell membrane

    Two types:

    1. Excititory Post Synaptic Potential (EPSP)

    -causes depolarization

    2. Inhibitory Post Synaptic Potential (IPSP)

    -causes hyperpolarization

    -inhibits postsynaptic cell (need larger

    stimulus to reach threshold)

    Multiple EPSPs needed to trigger action

    potential in post cell axon

    EPSP summation:

    1. Temporal summation

    -single synapse fires repeatedly: string of

    EPSPs in one spot

    -each EPSP depolarizes more until

    threshold reached at hillock

    Amy Warenda Czura, Ph.D. 9 SCCC BIO130 Chapter 12 Lecture Notes

  • 2. Spatial summation

    -multiple synapses fire simultaneously

    -collective depolarization reaches threshold

    Facilitated = depolarized; brought closer to

    threshold by some sort of stimulus, less

    stimulus now required to reach threshold

    (e.g. caffeine)

    Post Synaptic Potentiation:

    -repeat stimulation of same synapse

    conditions synapse, pre cell more easily

    stimulates post cell to threshold (repetition)

    Most nervous system activity results from

    interplay of EPSPs and IPSPs to

    promote differing degrees of facilitation

    or inhibition to allow constant fine

    tuning of response

    Neuromodulators = chemicals that influence

    synthesis, release, or degradation of

    neurotransmitters thus altering normal

    response of the synapse

    Common Neurotransmitters:

    1. Acetycholine- cholinergic synapses

    -excititory

    -direct effect

    -skeletal neuromuscular junctions, many

    CNS synapses, all neuron to neuron

    PNS, all parasympathetic ANS

    2. Norepinephrine- adrenergic synapses

    -excititory

    -second messengers

    -many brain synapses, all sympathetic ANS

    effector junctions

    3. Dopamine

    -excititory or inhibitory

    -second messengers

    -many brain synapses

    -cocaine: inhibits removal = high

    -Parkinsons disease: damage neurons =

    ticks, jitters

    4. Serotonin

    -inhibitory

    -direct or second messenger

    -brain stem for emotion

    -anti-depression/ anti-anxiety drugs

    block uptake

    5. Gamma aminobytyric acid (GABA)

    -inhibitory

    -direct effect

    -brain: anxiety control, motor coordination

    -alcohol: augments effects = loss of

    coordination

    Factors that disrupt neural function:

    1. pH: normal = 7.4

    @ pH 7.8 ! spontaneous action potentials

    = convulsions

    @ pH 7.0 ! no action potentials

    = unresponsive

    2. Ion concentrations

    high extracellular [K+] ! depolarize

    membranes = death, cardiac arrest

    3. Temperature: normal = 37C

    -higher: neurons more excitable

    (fever = hallucinations)

    -lower: neurons non-responsive

    (hypothermia = lethargy, confusion)

    4. Nutrients

    -neurons: no reserves, use a lot of ATP

    -require constant and abundant glucose

    -glucose only

    5. Oxygen

    -aerobic respiration only for ATP

    -no ATP = neuron damage/death

    Amy Warenda Czura, Ph.D. 10 SCCC BIO130 Chapter 12 Lecture Notes