Endocrine Flashcards
hormones that signal through cAMP
FLAT ChAMP
FSH, LH, ACTH, TSH
CRH, hCG, ADH, MSH, PTH
ant. pit. hormones
hormones that signal through IP3
GGOAT
GnRH, GHRH, Oxytocin, ADH, TRH
post. pit. hormones
steroid receptor hormones
VETTT CAP
vit D, estrogen, testosterone, T3/T4
Cortisol, Aldosterone, Progesterone
receptor tyrosine kinase hormones
PIG
prolactin, immunomodulators (cytokines), GH
stimulates bone and muscle growth
GH
stimulates milk production and secretion
prolactin
stimulates milk secretion during lactation
oxytocin
stimulates metabolic activity
thyroid hormone
increases blood glucose level and decreases protein synthesis
glucocorticoids
stimulates adrenal cortex to synthesize and secrete cortisol
ACTH
increases plasma calcium, increases bone resoprtion
PTH
decreases plasma calcium, increases bone formation
calcitonin
glucocorticoids
zona fasciculata of adrenal cortex
oxytocin
paraventricular n. of hypothalamus
atrial natriuretic hormone (ANH)
atria of heart
glucagon
a cells pancreas
vasopression (ADH)
supraoptic n of hypothalamus
calcitonin
parafollicular cells (c-cells)
epi and norepi
chromaffin cells of adrenal medulla
estradiol, estriol, estrone
ovaries, placenta, adipose
somatostatin
d-cells of pancreas
mineralocorticoids (aldosterone)
zona glomerulosa of adrenal cortex
clinical findings in man with high sex hormone binding globulin
gynecomastia (low testosterone)
clinical findings in woman with low sex hormone binding globulin
hirsutism (high testosterone)
which ant. pituitary hormones share the a subunit
TSH, LH, FSH, hCG
most likely clinical presentation of empty sella
asymptomatic
might have pit deficiency
most common presentation of hyperprolactinemia in female
premenopause: hypogonadism-infertility, oligo/amenorrhea
postmenopause: usually asymptomatic
might have galactorrhea in both
clinical features of acromegaly
increased size hands, feet, head,
coarse facial features
impaired glucose tolerance
inability to breastfeed, amenorrhea, cold intolerance
Sheehan syndrome
infertility, galactorrhea, and bitemporal hemianopsia
prolactinoma
adrenal gland from what tissue types
cortex: mesoderm
medulla: neural crest
adrenal secretory products
GFR
glomerulosa: aldosterone (mineralocorticoids)
fasciculata: cortisol, sex hormones (glucocorticoids)
reticularis: sex hormones (androgens)
medulla: chromaffin cells secrete catecholamines
adrenal steroid metabolism enzyme deficiency shortcut
if enzyme begins with #1: HTN
if second number in enzyme is 1: masculinization
ex: 11 hydroxylase def: HTN and masculinization
cortisol function
BBIIG maintains Blood pressure decreases Bone formation Immunosuppression/anti-Inflammatory increases Insulin resistance increases Gluconeogenesis
side effects of glucocorticoid use
BAM CUSHINGOID
buffalo hump, amenorrhea, moon facies, crazy, ulcers, skin changes, HTN, infection, necrosis of femoral head, glaucoma, osteoporosis, immunosuppression, diabetes
most common causes of Cushing syndrome
exogenous steroid use
ectopic ACTH secretion (small cell lung)
ACTH pit adenoma (Cushing Disease)
cortisol secreting adrenal tumor
treatment for nephrogenic DI
HCTZ, amiloride, indomethacin
HTN, hypokalemia, and metabolic alkalosis
hyperaldosteronism
hyperaldosteronism
Primary: adrenal hyperplasia or aldo adrenal adenoma (Conn’s)
Tx: surgery and/or spironolactone
Secondary: renal perceives low blood volume
Tx: spironolactone
hypotension, hyperkalemia, metabolic acidosis
adrenal insufficiency
Waterhouse-Friderichsen syndrome
acute primary adrenal insufficiency due to hemorrhage of adrenal cortex due to N. meningitidis
Addison’s disease
chronic primary adrenal insufficiency due to adrenal atrophy or destruction by disease