Adrenergic Pharmacology Flashcards
What catalyzes the conversion of l-DOPA to Dopamine?
A. Tyrosine hydroxylase
B. DOPA decarboxylase (AAADC)
C. Dopamine B-hydroxylase
D. Phenylethanolamine N-methyltransferase
B - aromatic l-amino acid decarboxylase (AAADC) catalyzes conversion
What inhibits the synthesis of l-DOPA to dopamine?
A. Carbidopa
B. tyrosine hydroxylase
C. a-methyltyrosine
D. a-methyldopa
A
______________ is used for pre-operative reduction of catecholamine synthesis in pheochromocytoma, a neuroendocrine tumor of the medulla.
A. Carbidopa
B. tyrosine hydroxylase
C. a-methyltyrosine
D. a-methyldopa
C - a-methyl tyrosine is a synthetic analog of tyrosine that inhibits tyrosine hydroxylase
_______ is a synthetic analog of tyrosine that inhibits tyrosine hydroxylase.
A. Carbidopa
B. DOPA decarboxylase
C. a-methyltyrosine
D. a-methyldopa
C
During autoregulation of neurotransmission, stimulation of ______________ adrenergic receptors inhibits norepinephrine release.
A. pre-synaptic a2
B. post-synaptic a2
C. pre-synaptic a1
D. pre-synaptic B2
E. post-synaptic B2
A
During autoregulation of neurotransmission, stimulation of ______________ adrenergic receptors potentiates norepinephrine release.
A. pre-synaptic a2
B. post-synaptic a2
C. pre-synaptic a1
D. pre-synaptic B2
E. post-synaptic B2
D
If a large amount of norepinephrine is released into the bloodstream, NE may act on distant effect cells. NE spillover is __________ in congestive heart failure.
A. increases
B. unchanged
C. decreases
A
What two types of drugs inhibit neuronal uptake of norepinephrine?
- Cocaine
- Tricyclic antidepressants
Active transport of norepinephrine through th emembrane by other tissues/organs/transporters is inhibited by ____________.
steroid hormones/corticosterone
The major metabolite from the final metabolic disposition of catecholamines is ____________.
vanillylmandelic acid
a-Methyldopa is a ___________ that functions as an anti-hypertensive.
A. presynaptic a1 agonist
B. presynaptic a2 agonist
C. postsynaptic a1 agonist
D. presynpatic a1 antagonist
E. postsynaptic a2 antagonist
B - a2 reduces central sympathetic outflow as an a2 agonist “false neurotransmitter”
Which functions to deplete NE from adrenergic terminals via inhibition of transporter systems of storage vesicles?
A. Bretilium
B. Guanethidine
C. Reserpine
D. Cocaine
E. a-methyldopa
C - resepine promots depletion and destruction of NE.
Which causes accumulation of NE at the receptor site due to inhibition of NE re-uptake?
A. Cocaine
B. TCAs
C. Bretilium
D. Guanethidine
E. A and B
F. C and D
E
Which drugs function to replace NE in vesicles and prevent norepinephrine release from storage vesicles?
A. Cocaine
B. TCAs
C. Bretilium
D. Guanethidine
E. A and B
F. C and D
F
a2 post-synaptic adrenergic receptors are located elsewhere on the vascular muscle cells and activated mainly by circulating catecholamines, but predominantly __________.
A. Epinephrine
B. Norepinephrine
C. Dopamine
D. None of these
A
__________ receptors are located close to the site of NE release and are mainly responsible for neuronal NE mediated vasoconstriction of smooth muscle.
A. a1 presynaptic
B. a1 postsynaptic
C. a2 presynaptic
D. a2 postsynaptic
B