Hypothalamic-pituitary CIS Flashcards

1
Q

What parts of the hypothalamus are the axons of the posterior pituitary gland located?

what type of communication occurs between the hypothalamus and the posterior pituitary?

A

supraoptic nucleus

paraventricular nucleus

communication is neural signaling

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2
Q

what does the posterior pituitary secrete and what are sources within hypothalamus of these hormones?

A

secretes neuropeptides

ADH from the SON

Oxytocin from the PVN

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3
Q

what are the three degreees of endocrine disorders?

A

1st degree: low or high levels of hormone due to defect in the peripheral endocrine gland

2nd degree: low or high levels of hormone due to defect in the pituitary gland

3rd degree: low or high levels of hormone due to defect in the hypothalamus

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4
Q

what is released by:

  • corticotroph
  • Thyrotroph
  • gonadotroph
  • somatotroph
  • lactotroph
A

Corticotroph: ACTH

Thyrotroph: TSH

Gonadotroph: FSH, LH

Somatotroph: GH

Lactotroph: Prolactin

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5
Q
A

answer is prolactin because if you resect hypothalamus you wouldnt have dopamine to inhibit.

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6
Q

Hypothalamic- Anterior Pituitary hormone relationships

hormones from hypothalamus target what in anterior pituitary, which secrete what products?

A
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7
Q

Important implications of the hypothalamic-hypophysial portal vessels

2

A
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8
Q

what is the pathophysiology of acromegaly?

why prolactin elevated?

why ammenorhea?

A

high level of growth hormone

IGF-1 is also high

see high fasting glucose in these patients

tumor may compress stalk, disrupt release of dopamine into AP to suppress prolactin

tumor affecting pituitary causing it not to release FSH/LH

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9
Q

what does GH stimulate?

A

stimulates somatomedin C (IGF-1) gene transcription and secretion by the liver

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10
Q

Draw a diagram of the endocrine axis regulating GH secretion

A
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11
Q

Pathophysiology of acromegaly

Primary GH excess

Extrapituitary GH excess

GHRH excess

A
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12
Q

Diagnosis of acromegaly

A
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13
Q

medications for acromegaly

A

octreotide/lanreotide: somatostatin analogs

Pegvisomant: GH receptor antagonist

Bromocriptine/carbergoline: dopamine receptor agonists

-may decrease GH secretion, only small portion of patients are responsive to this therapy

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14
Q

what age is GH highest? lowest?

A
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15
Q

Pathophysiology of GH

-deficiency mechanisms?

excess before puberty leads to?

A

GH deficiency can come from decrease in GHRH (hypothalamic dysfxn), decrease in GH secretion (primary deficiency), failure to generate somatomedins, GH or somatomedin resistance (deficiency of receptors)

Excess before puberty leads to gigantism

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16
Q

GH acts on which type of cell to cause bone growth?

A

chondrocytes

17
Q

what are the metabolic functions of GH?

  • Diabetogenic mechanism
  • Protein synthesis mechanism
  • Linear growth mechanism
A
18
Q

Nutritional status and how it relates to GH, IGF-1, and insulin?

A
19
Q
A

lactotrophs

20
Q

What happens with high prolactin levels?

A

often amenorrhea, suppresses FSH and LH

21
Q

what is secreted in cushings disease associated pituitary adenoma?

A

ACTH

22
Q

Sheehan syndrome

  • what is it?
  • Typical pt presentation
A
23
Q

45 year old woman has CVA that causes necrosis of the posterior pituitary. which of the following effect is most likely seen?

inability to lactate, hypothyroidism, hypoglycemia, or hypernatremia

A

hypernatremia, but kinda bullshit

24
Q

What are the triggers of ADH secretion?

most sensitive to what?

A

decreased BP, decreased arterial stretch due to low blood volume, increase in osmolarity

most sensitive to osmolarity changes

25
Q

what is mechanism of action of ADH in renal collecting tubule?

A
26
Q

Central vs. nephrogenic diabetes insipidus

A
27
Q

How does the water deprivation test for DI work?

A
28
Q

What is the pathophysiology of SIADH and what is its treatment?

A
29
Q
A