HP Relationships Flashcards

(44 cards)

1
Q

What is the pituitary gland (hypophysis) composed of?

A
anterior pituitary (adenohypophysis) - epithelial portion
posterior pituitary (neurohypophysis) - neural portion
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2
Q

What is the hypophysial stalk?

A

physical connection between the hypothalamus and pituitary gland

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3
Q

What is the posterior pituitary a collection of, and what does it secrete?

A

collection of axons whose cell bodies and located in the hypothalamus: supraoptic nucleus (SON) and paraventricular nucleus (PVN)

it secretes neuropeptides: ADH (mostly SON) and oxytocin (mostly PVN)

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4
Q

What hormones does the anterior pituitary secrete?

A

ACTH, TSH, FSH, LH, GH, prolactin

anterior pituitary is connected to hypothalamus by hypothalamic-hypophysial portal vessels

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5
Q

What are two important implications of the hypothalamic-hypophysial portal vessels?

A
  1. hormones can be delivered to the anterior pituitary directly and in high concentration
  2. hormones do not appear in the systemic circulation in high concentration
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6
Q

What is a primary endocrine disorder?

A

low or high levels of hormone due to defect in peripheral endocrine gland

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7
Q

What is a secondary endocrine disorder?

A

low or high levels of hormone due to defect in pituitary gland

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8
Q

What is a tertiary endocrine disorder?

A

low or high loevels of hormone due to defect in the hypothalamus

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9
Q

What hormones do corticotrophs release?

A

ACTH

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10
Q

What hormones do thyrotrophs release?

A

TSH

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11
Q

What hormones do gonadotrophs release?

A

FSH and LH

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12
Q

What hormones do somatotrophs release?

A

GH

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13
Q

What hormones do lactotrophs/mammotrophs release?

A

prolactin

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14
Q

What causes acromegaly?

A

prolonged, excessive secretion of GH in adult life
characterized by excessive growth of soft tissue, cartilage and bone in face, hands and feet - develops very gradually
can lead to HTN, accelerated osteoarthrosis, hyperglycemia, cardiomegaly
-> GH acts on chondrocytes

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15
Q

What does GH stimulate?

A

somatomedin C (insulin-like growth factor 1, IGF-1) gene transcription and secretion by the liver

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16
Q

How do you diagnose acromegaly and what are the medications given?

A

increase in serum IGF-1 levels, failure to supress serum GH following OGTT, pituitary mass seen on brain MRI

octoreotide/lanreotide (somatostatin analog)
pegvisomant (GH receptor antagonist)
bromocriptine/cabergoline (dopamine receptor agonists)

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17
Q

What leads to a GH deficiency?

A

decreased secretion of GHRH
decreased secretion GH
failure to generate somatomedins
GH or somatomedin resistance

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18
Q

What leads to a GH excess?

A

mostly due to a growth hormone-secreting pituitary adenoma
consequences depend on developmental stage
- before puberty = gigantism
- after puberty = acromegaly

19
Q

What is the diabetogenic effect?

A

increase in blood glucose concentration

  • causes insulin resistance
  • decrease in glucose uptake and utilization by target tissues
  • increase in lipolysis in adipose tissue
  • results in increase in blood insulin levels
20
Q

What do somatomedins (IGF-1) mediate?

A

increase in protein synthesis, organ growth and linear growth

21
Q

What does hyperprolactinemia supress?

A

FSH and LH secretion

22
Q

What is the function of CRH?

A

increase ACTH, MSH

23
Q

What is the function of dopamine?

A

decrease prolactin

24
Q

What is the funtion of GHRH?

25
What is the function of GnRH?
increase FSH, LH
26
What is the function of prolactin?
decrease GnRH
27
What is the function somatostatin?
decrease GH, TSH
28
What is the function of TRH?
increase in TSH, prolactin
29
What causes Cushing's disease?
high levels of ACTH
30
What causes TSH-secreting adenoma?
high levels of TSH
31
What causes acromegaly/gigantism?
high levels of GH
32
What causes prolactinoma?
high levels of prolactin
33
What causes a non-functioning adenoma?
high levels of LH and FSH
34
What are the causes of hypopituitarism?
brain damage, pituitary tumors, non-pituitary tumors, infections, infarction, autoimmune disorders, pituitary hypoplasia
35
What is Sheehan syndrome?
postpartum hypopituitarism due to necrosis of the pituitary gland most patients present with agalactorrhea (difficulties with lactation) amenorrhea (lack of menstruation), hypothyroidism
36
What are the posterior lobe neuropeptides?
ADH, oxytocin
37
What are the posterior lobe secreting neurons?
ADH (mainly from supraoptic nuclei) | oxytocin (mainly from PVN)
38
What are the triggers of ADH secretion?
decrease in blood pressure (baroreceptor reflex) decrease in arterial strethc due to low BV (atrial stretch receptors_ increase in osmolarity (hypothalamic osmoreceptors) NOTE: secretion most sensiive to plasma osmolarity changes
39
What happens to ADH in hyperosmolar state?
hypothalamus detects too little water -> pituitary gland release ADH -> kidneys remove less water from the blood so less water is lost in urine
40
What happens to ADh in a hypo-osmolar state?
hypothalamus detects too much water in blood -> pituitary gland release less ADH -> kidneys remove more water from blood so more water is lost in urine
41
What is diabetes insipidus?
lack of an effect of ADH on the renal collecting duct causes frequent urination large volume of urine is diluted
42
What is central DI?
lack of ADH could result from damage to the pituitary, or destruction of the hypothalamus tx: desmopressin
43
What is nephrogenic DI?
kidneys unable to respond to ADH causes: drugs like lithium, chronic kidney disorders (polycystic kidney disease) CANNOT treat with desmopressin (does NOT respond to ADH)
44
What is syndrome of inappropriate ADH secretion (SIADH)?
excessive secretion of ADH excessive water retention hypo-osmolarity fails to inhibit ADH release