Hypothalamus and pituitary lecture Flashcards
What is the coordinating center of the endocrine system
hypothalamus
Where is the pituitary gland
sella tursica in the sphenoid bone
another name for anterior pituitary
adenohypophysis
what is the anterior pituitary
highly vascularized
regulates thyroid, adrenal, mammary glands
regulated GH, gonads, melanocytes
adrenal glands- major
thyroid, adrenals, gonads
anterior pituitary cell types
somatotrops (30-40%) most abundant, secretes GH
Croticotropes (20%) secretes ACTH
Thyrotropes (5%) secretes TSH
Gonadotropes (5%) secretes LH and FSH
Lactrotropes (5%) secretes prolactin
The posterior pituitary is aka
neurohypophysis
produces adh and oxytocin
where is blood supplied from when it goes to the hypothalamus, AP, and PP
hypothalamus- superior hypophyseal artery
AP- long portal vessels
PP- inferior hypophyseal artery
names and function of the nuclei in the hypothalamus
paraventricular- oxytocin (pitocin)
supraoptic nucleus- ADH
what is the master gland
pituitary gland
anterior pituitary secretes:
FLAT PG
fsh
lh
acth
thyroid/ tsh
prolactin
gh
stimulus for adh release- what is activated?
high plasma osmolarity >290 activate
osmoreceptor in hypothalamus
decreased ecf volume
increased na, low bp, at2, nicotine, pain, ppv,
DI
adh deficiency
neurogenic (common) or nephrogenic
what can cause nephrogenic di
ckd
lithium toxicity
hypercalcemia
hypokalemia
drugs (tubulointerstitial disease)
genetics
anesthesia and hypernatremia
increased mac
decreased ecf requires lower iv doses
postpone if over 150
lethargy, hyperreflexia, restlessness
siadh
water
adh overload
restrict fluids, demeclocycline
anesthesia and hyponatremia (stop level, mac, symptoms, tx)
cancel if below 130
<130 decrease in mac
agitation, confusion, somnolence
3% saline, lasix
risk factors for central pontine myelinolysis
sodium >120 for 48 hours
aggressive iv fluid therapy with 3%
development of hypernatremia during treatment
monitor q1h
where is oxytocin secreted from
paraventricular nucleus of posterior pituitary
what is the action of oxytocin
contract uterus during labor- used after labor to stop blood loss after birth
contract lactating breast
risks of oxytocin
fetal distress due to hyperstimulation
uterine tetany
maternal water intoxication
rapid infusion can cause htn, tachy, nv, seizures
how do pituitary tumors present
eye issues
bitemporal hemianopsia
excess GH presentation
acromegaly, difficult mask and intubation
excess tsh presentation
hyperthyroid, tachy, weight loss
acth excess presentaiton
cushings, difficult airway and access
treatment for panhypopituitarism
cortisol
t4
ddavp
pituitary surgery approach
most done with transphenoidal approach
some may require craniotomy
risks (and tx) of pituitary surgery
di
suspect with urine spec gravity <1.005
treat with ddavp 2mcg iv or sq and volume
anesthetic considerations for pituitary surgery
normotensive and normocapneic
hypocapnea will lower icp
deep extubate
oral rae
acromegaly presentation
large tongue, large epiglottis, enlarged mandible, distorted anatomy
subglottic narrowing, vocal cord enlargement
downszie ett
osa, htn, cmp, lvh common
skeletal overgrowth
glucose intolerance
entrapment nueropathys
most common cause of di
pituitary surgery
but also
tbi
sah
ddavp dose for di
sc- 0.5-2mcg bid
nasal- 5-40 mcg qd
treatment for siadh
fluid restriction
3%
demeclocycline
most common cause of siadh
tbi - most
small cell lung carcinoma
carbamazepine
another name for growth hormone
somatotropin
main cause of acromegaly
pituitary adenoma
acromegaly vs gigantism
acromegaly- after adolescence
gigantism- before puberty
t3 vs t4
t3- more potent, shorter half life, less protein bound
t4- prohormone, less potent, more concentrations in the blood
half life of t3 and t4
t3- 1 day
t4- 7 days
acromegaly considerations
distorted facial features- difficult mask ventilation
Large tongue, teeth, epiglottis- difficult laryngoscopy
subglottic narrow and vocal cord enlargement- use smaller tube
turbinate enlargements- risk of epistaxis, avoid nasal intubation if possible
osa common
htn, cad, rhythm disturbance
glucose intolerance
sm weakness
entrapment neuropathy- ulnar
what do patients with hyperparathyroid present with often?
increased PTH and hypophosphatemia
clinical feature of primary hyperparathyroidism
shortened qt from hypercalemia
pathological fx from bone resportion
hypocalcemia can cause
laryngospams
myocardial depression