Physio 2 Flashcards

1
Q

growth hormone

A

single chain polypeptide. produced in anterior pituit. 20 minute half life.

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2
Q

hypothalamic control of GH secretion

A

GHRH stimulates, somatostatin inhibits. integration results in episodic pulsatile secretion.

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3
Q

GHRH

A

increases GH gene transcription, promotes GH release, stimulates production of GHRH receptor, stimulates somatostatin release

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4
Q

somatostatin

A

decreases pulse freq, decreases pulse amplitude, no impact on GH synth, inhibits GHRH release

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5
Q

ghrelin

A

made in stomach and pancreas. stimulates hunger. levels increase before meals, decrease after, acts on growth hormone secretagogue receptor.

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6
Q

pulsatile secretion of GH over lifespan

A

pulses primarily at night. number of pulses per day stays nearly constant. larger pulse amplitude during puberty. exercise can cause a surge of GH. disrupting sleep can cause lack of GH

obesity decreases number and duration of GH pulses.
fasting increases number and amplitude of GH pulses.

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7
Q

stimulators of GH secretion

A

sleep, exercise, sex steroids, fasting, amino acids, stress, alpha adrenergic agonists, dopamine agonists

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8
Q

inhibitors of GH secretion

A

IGH-1, obesity, glucocorticoids, hyperglycemia, free fatty acids, GH, beta adrenergic agonists

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9
Q

GH activation of receptor

A

binding of GH changes arrangement of receptor dimer and activates JAK2. JAK2 phosphorylates and activates STAT transcription factors. STAT activates CISH, a GH target gene

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10
Q

effects of GH on liver, adipose, skeletal muscle, and brain

A

liver: stimulates IGF-1 production, and stimulates hepatic glucose production
adipose: GH stims release and oxidation of fatty acids and reduces lipogenesis
skeletal muscle: GH stimulates AA uptake and incorporation into protein, and stims cell proliferation
brain: affects mood and behavior

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11
Q

effect of GH on bone

A

GH supports the differentiation of mesenchymal stem cells into chondrocytes and maturation of chondrocytes. this leads to bone formation

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12
Q

IGH-1

A

stimulates growth through autocrine, paracrine, and endocrine methods. negative feedback to the hypothalamus and pituitary down regulates GH secretion. used as the primary screening test for GH deficiency (levels are more stable and reflective of GH levels)

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13
Q

signaling pathways activated by IGF-1

A

dimerization of IGF-1 receptor leads to autophosphorylation. this recruits IRS-1 and Shc, both of which get phosphorylated. this recruits other proteins leading to the activation of PI3K and Ras/MAP kinase pathways that regulate cellular transcription

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14
Q

growth hormone deficiency causes

A

rare causes. any defect affecting hypothalamo-pituitary function, mutations in GH-1 gene, brain injury, absence of pituitary stalk etc..
causes extremely slow growth rate of less than two inches a year

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15
Q

Laron syndrome

A

point mutation or deletion in GH receptor. leads to low IGF-1 concentration, but normal or elevated GH concentration. severe post natal growth failure. treatable with rhIGH-1

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16
Q

gigantism

A

usually pituitary giants. too much GH in life. usually have hyperglycemia and 10% develop diabetes mellitus

17
Q

acromegaly

A

growth hormone secreting adenomas cause this. effects vary. protrusion of jaw, enlarged tongue (macroglossia), enlarged hands and feet, carpal tunnel etc

18
Q

GH deficiency in adults

A

usually pituitary problems. increased interstitial fat, reduced strength and bone loss. anxiety, depression.
increases clotting factors, LDL, and insulin resistance. can lead to cardiovascular disease. decreases HDL

treat with rhGH.

19
Q

what is GH therapy approved for?

A

GH deficiency, idiopathic short stature, turner syndrome, prader-willi syndrome, chronic renal insufficiency, small for gestational age

20
Q

short stature in turner syndrome

A

insuffiency of SHOX gene. SHOX protein is concentrated in the hypertrophic region of the growth plate zone during childhood. without it, you have slower velocity during childhood, and a scant pubertal growth spurt