2402 ch 17 endocrine system (part 2) ppt.pdf
TRANSCRIPT
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II. Characterize Selected Glands ! Hypothalamus ! Pituitary gland ! Growth Hormone
! Thyroid gland ! Parathyroid glands ! Adrenal glands ! Pancreas ! Gonads ! Pineal Gland
! Location ! Anatomy/Histology ! Regulation !Hormonal, humoral,
nervous ! Hormones ! Functions !Target cell & actions
on target cells ! Diseases
(homeostatic imbalances) 49
50
Characterize the hypothalamus gland:
! Master endocrine gland
(along w/
pituitary)
! Location
! Functions
! Hypophyseal portal system
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Hypothalamus: Master Controller
of Endocrine System
! Hypothalamus secretes regulatory (releasing) hormones that travel through the hypothalamo-hypophyseal portal system to the anterior pituitary and release
! Tropic (stimulating) hormones from the anterior pituitary that travel in the general circulation to other glands in the body and stimulate
! The secretion of hormones from those glands. ! Hypothalamus " anterior pituitary " glands in body
Fig. 17.14 p. 671
Hypothalamus " anterior pituitary " glands in body
Releasing hormones: TRH, PRH, GnRH, CRH, GHRH Inhibiting hormones: PIH, GIH
Regulatory hormones of hypothalamus Tropic hormones of anterior pituitary
Thyroid-stimulating hormone (TSH) stimulates thyroid gland to release thyroid hormone.
Anterior pituitary Posterior pituitary
Infundibulum
Muscle
Prolactin (PRL) acts on mammary glands to stimulate milk production.
Follicle-stimulating hormone (FSH) and luteinizing hormone (LH) act on gonads (testes and ovaries) to stimulate development of gametes (sperm and oocyte).
Testis Ovary
Thyroid
Mammary gland
TSH Growth hormone (GH) acts on all body tissues, especially cartilage, bone, muscle, and adipose connective tissue to stimulate growth.
Adipose connective tissue
Bone
Adrenal cortex
Adrenocorticotropic hormone (ACTH) acts on the adrenal cortex to cause release of corticosteroids (e.g., cortisol).
Adrenal gland
FSH and LH
GH
ACTH
Hypothalamus
PRL
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Names & functions of hormones produced by the hypothalamus:
Table 17.3 p. 670
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Characterize the pituitary gland: ! Anatomy
! Infundibulum ! 2 Lobes/3 Sections:
! Anterior pituitary (adenohypophysis)
! Posterior pituitary (neurohypophysis)
! Intermedia
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Name & Function of Adenohypophyseal (Anterior Pituitary) hormones:
! HM of anterior pituitary controlled by releasing or inhibiting HM produced by hypothalamus
-TSH
-PRL
-FSH
-LH
-ACTH
-GH
-MSH
Hormone Function
Melanocyte-stimulating hormone (MSH) stimulates synthesis of melanin and distribution of melanocytes in skin (little effect in humans)
Table 17.4 p. 672
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Mnemonic Device
Page 672
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Discussion of Pituitary Hormone Effects
1. Growth Hormones effects on multiple organ systems
2. posterior pituitary hormones (ADH & oxytocin)
3. The effects of other anterior pituitary hormones will be discussed with the particular gland they effect.
Nutrient Metabolism is altered by many hormones, including GH
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Effects of anterior pituitary human growth hormone & insulinlike growth factors:
! GH promotes secretion of Insulinlike Growth Factors (IGFs)
! Indirect functions of GH via IGFs ! target cells = liver, skeletal muscle, cartilage & bone ! increases cell growth & division ! stimulate lipolysis ! retard use of glucose for ATP production
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Metabolic action of GH:
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Describe the regulation of GH: ! Antagonistic hypothalamic
HM regulate GH ! GHRH stimulates GH
release ! GIH (aka GHIH) inhibits GH
release
! Hypoglycemia stimulates release of GHRH from hypothalamus
! Hyperglycemia & high levels of GH/IGFs ! Inhibit GHRH & GH release ! Stimulate GIH release
What Stimulates
GHRH Secretion?
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3 3 4
7 8
5 6
6
Growth hormone
Stimulation Inhibition STIMULUS
Variables that influence the release of GHRH from the hypothalamus:
Age
Nutrient levels in the blood Stress and exercise
Time of day
Hypothalamus
CONTROL CENTER RECEPTOR
Increased levels of both GH and IGF inhibit the release of GHRH from the hypothalamus; Increased levels of GH also inhibits the release of GH from the anterior pituitary.
NET EFFECT
Increased protein synthesis, mitosis, and cell differentiationespecially in cartilage, bone, and muscle; release of stored nutrients into the blood.
Amino acids
Bone Muscle
EFFECTORS: Effectors respond to GH and/or IGF in the following ways:
Increased growth Increased amino acid uptake which results in protein synthesis Stimulated mitosis
Cell differentiation
Increased lipolysis
Decreased lipogenesis
Increased glycogenolysis and gluconeogenesis Decreased glycogenesis
Adipose connective tissue
Liver tissue
In response to GHRH, the anterior pituitary releases growth hormone (GH).
GH stimulates hepatocytes to release insulin-like growth factor (IGF) into the blood.
Both GH and IGF stimulate target cells (effectors).
The hypothalamus releases growth hormonereleasing hormone (GHRH) into the hypothalamo-hypophyseal portal system.
The hypothalamus responds to various stimuli.
GH
IGF
GH
GH
IGF
Hepatocytes
Liver
GH
Glycerol Fatty acids Glucose
All cells
GHRH
GH
5 4
IGF
2 2 1
1 Good Summary: Fig. 17.15 on p. 674
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What are the effects of excess growth hormone?
! Diabetogenic effect of GH
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Clinical Applications:
! Hyposecretion hGH ! childhood = Hypopituitary
dwarfism
! Hypersecretion hGH ! childhood = giantism ! adult = acromegaly
http://www.chauvet-translation.com/figures/Figure027.jpg
Jyoti Amge Smallest girl in the world
Pituitary dwarfism is a condition that exists at birth as a result of inadequate growth hormone production due to a hypothalamic or pituitary problem. Growth retardation is typically not evident until a child reaches 1 year of age, because the influence of growth hormone (GH) is minimal during the first 6 to 12 months of life. In addition to short stature, children with pituitary dwarfism often have periodic low blood sugar (hypoglycemia). Injections of growth hormone over a period of many years can bring about improvement, but not a normal state. Too much growth hormone causes excessive growth and leads to increased levels of blood sugar. Oversecretion of growth hormone in childhood causes pituitary gigantism. Beyond extraordinary height (sometimes up to 8 feet), these people have enormous internal organs, a large and protruding tongue, and significant problems with blood glucose management. If untreated, a pituitary giant dies at a comparatively early age, often from complications of diabetes or heart failure.
leads to a protruding jaw (prognathism). Internal organs, especially the liver, increase in size, and increased release of glucose lead to the development of diabetes in virtually everyone with acromegaly. Acromegaly may result from loss of feedback control of growth hormone at either the hypothalamic or pituitary level, or it may develop because of a GH-secreting tumor of the pituitary. Removal of the pituitary alleviates the effects of acromegaly, but this drastic treatment results in the loss of all pituitary hormones.
Pituitary dwarfism
Gigantism
Age 52
Age 16 Age 9
Age 33 Acromegaly
CLINICAL VIEW Disorders of Growth Hormone Secretion
INTEGRATE
Excessive growth hor- mone production in an adult results in acromegaly. The individual does not grow in height, but the bones of the face, hands, and feet enlarge and widen (appositional growth), along with growth in cartilage. An increase in mandible size
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Characterize the posterior pituitary gland (neurohypophysis)
! Hypothalamo-hypophyseal tract ! Axon terminals of
hypothalamic neurons
! No hormone synthesis ! Stores/releases
ADH & oxytocin
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Characterize oxytocin:
! Two target tissues: ! Both involved in
neuroendocrine reflexes
! During delivery = uterus ! After delivery = breasts
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Recall the function of antidiuretic hormone (ADH) aka vasopressin
! decrease urine production
! decrease sweating
! increase BP
Describe the regulation of
ADH: ! ADH released when
blood osmotic pressure
is high (dehydration or
blood loss)
! ADH inhibited when blood osmotic pressure
is low (increased blood
volume)
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Clinical Application: ! Central or pituitary diabetes insipidus
! kidneys are unable to conserve water
! Etiology damage to hypothalamus or pituitary
! Sx excessive thirst & urination
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Characterize the thyroid gland: ! Location
! 2 lobes either side of trachea ! Connected by isthmus
! Functions
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Describe the histology of
thyroid gland:
! Consists of follicles ! Follicular cells ! Thyroglobulin ! T3 & T4
! Parafollicular cells ! Calcitonin
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Functions of T3 & T4 ! Increase BMR (basal
metabolic rate)
! Stimulate protein synthesis
! Increase use of glucose & fatty acids for ATP production
! Heat production ! Regulating tissue growth # Developing skeletal & nervous systems
Functions Calcitonin ! Parafollicular cells or C cells produce calcitonin
! peptide HM ! Lowers blood Ca2+ by inhibiting bone
resorption ! Inhibits osteoclast activity (& thus bone
resorption) & release of Ca+2 from bone matrix
! Stimulates Ca+2 uptake & incorporation into bone matrix
! Antagonist to parathyroid hormone (PTH)
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Mechanism of Thyroid
Hormone Production
Know Figure 17.18
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Low blood levels of T3 and T3 or low metabolic rate stimulate release of
Hypothalamus TRH
Actions of Thyroid Hormones:
Increase basal metabolic rate Stimulate synthesis of Na+/K+ ATPase
Increase body temperature (calorigenic effect) Stimulate protein synthesis
Increase the use of glucose and fatty acids for ATP production Stimulate lipolysis
Enhance some actions of catecholamines Regulate development and growth of nervous tissue and bones
1
Anterior pituitary
TRH, carried by hypophyseal portal veins to
anterior pituitary, stimulates
release of TSH by thyrotrophs
Low blood levels of T3 and T3 or low metabolic rate stimulate release of
Hypothalamus
TSH
TRH
Actions of Thyroid Hormones:
Increase basal metabolic rate Stimulate synthesis of Na+/K+ ATPase
Increase body temperature (calorigenic effect) Stimulate protein synthesis
Increase the use of glucose and fatty acids for ATP production Stimulate lipolysis
Enhance some actions of catecholamines Regulate development and growth of nervous tissue and bones
1
2
Anterior pituitary
TRH, carried by hypophyseal portal veins to
anterior pituitary, stimulates
release of TSH by thyrotrophs
TSH released into blood stimulates
thyroid follicular cells
Thyroid follicle
Low blood levels of T3 and T3 or low metabolic rate stimulate release of
Hypothalamus
Anterior pituitary
TSH
TRH
Actions of Thyroid Hormones:
Increase basal metabolic rate Stimulate synthesis of Na+/K+ ATPase
Increase body temperature (calorigenic effect) Stimulate protein synthesis
Increase the use of glucose and fatty acids for ATP production Stimulate lipolysis
Enhance some actions of catecholamines Regulate development and growth of nervous tissue and bones
1
2
3
T3 and T4 released into
blood by follicular cells
TRH, carried by hypophyseal portal veins to
anterior pituitary, stimulates
release of TSH by thyrotrophs
TSH released into blood stimulates
thyroid follicular cells
Thyroid follicle
Low blood levels of T3 and T3 or low metabolic rate stimulate release of
Hypothalamus
Anterior pituitary
TSH
TRH
Actions of Thyroid Hormones:
Increase basal metabolic rate Stimulate synthesis of Na+/K+ ATPase
Increase body temperature (calorigenic effect) Stimulate protein synthesis
Increase the use of glucose and fatty acids for ATP production Stimulate lipolysis
Enhance some actions of catecholamines Regulate development and growth of nervous tissue and bones
1
2
3
4 T3 and T4 released into
blood by follicular cells
Elevated T3inhibits release of TRH and
TSH (negative feedback)
TRH, carried by hypophyseal portal veins to
anterior pituitary, stimulates
release of TSH by thyrotrophs
TSH released into blood stimulates
thyroid follicular cells
Thyroid follicle
Low blood levels of T3 and T3 or low metabolic rate stimulate release of
Hypothalamus
Anterior pituitary
TSH
TRH
Actions of Thyroid Hormones:
Increase basal metabolic rate Stimulate synthesis of Na+/K+ ATPase
Increase body temperature (calorigenic effect) Stimulate protein synthesis
Increase the use of glucose and fatty acids for ATP production Stimulate lipolysis
Enhance some actions of catecholamines Regulate development and growth of nervous tissue and bones
1
2
3
5
4
T3 & T4 Secretion Regulation
! Hypothalamus secretes TRH in response to
blood levels of T3 & T4
! TRH # secretion of TSH from anterior pituitary
! TSH stimulates synthesis/secretion of T3 & T4
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Good Summary
Figure 17.19
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Clinical Application: Thyroid Gland Disorders ! Hypothyroidism
! Congential # Cretinism ! Adult # Myxedema
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Clinical Application: Thyroid Gland Disorders
! Hyperthyroidism (Graves disease)
! Goiter = enlarged thyroid (dietary)
Page 678
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Characterize the parathyroid glands: ! 4 glands embedded in
lobes of thyroid gland ! Chief (Principal) cells ! Oxyphil cells
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Describe the mechanism of action of PTH:
! Parathyroid hormone (PTH) or parathormone ! Major regulator of Ca+2,
Mg, & phosphate ions in blood
! Increases number & activity of osteoclasts
! Elevates bone resorption
! Blood Ca+2 level directly controls secretion of both calcitonin & PTH via (-) feedback
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Parathyroid Hormones
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Blood Calcium Regulation
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Clinical Application: Hyperparathyroidism
! Parathyroid adenoma #1 cause ! Serum calcium imbalance