Thyrotropin-releasing hormone (TRH) infusion causes
-   stimulation of prolactin release by the pituitary
 -   inhibition of thyroxine production
 -   stimulation of ACTH production by the pituitary
 -   stimulation of growth hormone production
 -   all of the above
 
 
Serum thyrotropin levels in hyperthyroidism:
-   enhanced
 -   suppressed
 
 
TSH fails to rise after TRH administration: this clinical condition is most likely:
-   primary hyperthyroidism
 -   secondary (pituitary) hypothyroidism
 -   both
 -   neither
 
 
Unusual pituitary tumor cell responses to TRH may result in:
-   acromegaly
 -   Cushing's disease
 -   prolactin release failure
 -   none of the above
 -   A, B & C
 
 
Thyroid-stimulating hormone (thyrotropin, TSH) is synthesized at this site:
-   hypothalamus
 -   anterior pituitary
 
 
TSH subunit that confers thyroid specificity:
-   alpha
 -   beta
 -   both
 -   neither
 
 
Mechanism of thyrotropin action -- results in ultimately increased thyroid hormone production:
-   activation of thyroid cell IP3 system
 -   activation of guanylyl cyclase system
 -   activation of adenylyl cyclase system
 -   blockade of beta adrenergic receptors
 -   through alpha adrenergic receptor antagonism
 
 
Primary thyrotropin (TSH) degradation site:
-   liver
 -   kidney
 -   excreted unchanged; no degradation
 
 
Hypothalamic hormone causing pituitary release of beta-endorphins and ACTH:
-   TRH
 -   TSH
 -   CRH
 -   adrenocorticotropin
 
 
ACTH adrenocortical stimulation results in:
-   cholesterol esterases activity
 -   reduced mineralocorticoid production
 -   adrenal atrophy
 -   skin depigmentation