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79 Cards in this Set
- Front
- Back
blocks VMAT2? |
reserpine |
|
blocks DAT? |
cocaine |
|
sympathetic neurons do not have which NT breakdown catalyst? |
COMT |
|
tri-cyclic antidepressants block? |
NET |
|
additional enzyme required to synthesize epinephrine? |
PNMT |
|
12 membrane spanning domains describe what? |
VMAT2, DAT, NET (transporters) |
|
VMAT2 needs what to function? |
protons inside vesicle and ATP powered proton pump to pump them out |
|
what do the transporters DAT and NET depend on? |
sodium gradient |
|
which forms of MAO exist? |
A and B |
|
what can those on MAO's not eat? |
dairy products |
|
oxymetazoline |
adrenergic agonist, direct-acting, non-selective, alpha-1,2 |
|
ephedrine |
adrenergic agonist, mixed-acting, alpha-1,2, beta-1,2 and releasing agent |
|
amphetamine |
adrenergic agonist, indirect-acting, releasing agent |
|
tyramine |
adrenergic agonist, indirect-acting, releasing agent |
|
cocaine |
adrenergic agonist, indirect-acting, uptake inhibitor |
|
selegiline |
adrenergic agonist, indirect-acting, MAO inhibitor (B form) |
|
corgyline |
adrenergic agonist, indirect-acting, MAO inhibitor (A form) |
|
pargyline |
adrenergic agonist, indirect-acting, MAO inhibitor (B form) |
|
entacapone |
adrenergic agonist, indirect-acting, COMT inhibitor |
|
pyrogallol |
adrenergic agonist, indirect-acting, COMT inhibitor |
|
tropolone |
adrenergic agonist, indirect-acting, COMT inhibitor |
|
responses are not reduced by prior treatment with reserpine or guanethidine but may be potentiated by cocaine, reserpine, and guanethidine for which categories? |
selective and non-selective, direct acting, adrenergic agonists |
|
response is reduced by prior treatment with reserpine or guanethidine? |
mixed acting, adrenergic agonists (ephedrine) |
|
responses are abolished by prior treatment with reserpine or guanethidine? |
indirect-acting, adrenergic agonists that are releasing agents (amphetamine, tyramine) |
|
phenoxybenzamine |
adrenergic antagonist, alpha receptor, non-selective irreversible via covalent modification |
|
phentolamine |
adrenergic antagonist, alpha receptor, non-selective reversible |
|
prazosin* |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control more effective in alpha-1 than alpha-2 (1000 times) lasts 7-10 hours |
|
terazosin* |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control better for BPH than prazosin because higher affinity for alpha-1a receptor |
|
doxazosin* |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control good for BPH, high selectivity for alpha-1, long lasting (not necessarily good) |
|
alfuzosin* |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control good for BPH, similar affinity for all alpha-1 receptors, shorter acting |
|
tamsulosin* |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control used to treat BPH w/ little effect on BP, selective for alpha-1a,d over b |
|
indoramin |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control |
|
urapidil |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control |
|
bunazosin |
adrenergic antagonist, alpha receptor, alpha-1 selective vascular resistance control |
|
yohimbine* |
adrenergic antagonist, alpha receptor, alpha-2 selective pulled off market, now supplement increase in blood pressure and HR |
|
nadolol* |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels treats HTN, angina and is long acting |
|
penbutolol |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels |
|
pindolol* |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels treats HTN, angina, 4 hr half life |
|
propranolol* |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels treats HTN, angina, arrhythmias/tachycardia some intrinsic sympathetic activity causing bronchodilation in normal pt |
|
timolol* |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels treats HTN, CHF, acute MI, migraine, open angle glaucoma, intraocular HTN |
|
sotalol |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels |
|
levobunolol |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels |
|
metipranolol |
adrenergic antagonist, beta receptor, non-selective, first generation membrane stabilization properties via blockage of voltage gated Na channels |
|
acebutolol* |
adrenergic antagonist, beta receptor, beta-1 selective, second generation treats HTN, ventricular/atrial arrhythmias, acute MI, some intrinsic sympathetic activity and membrane stabilization activity |
|
atenolol* |
adrenergic antagonist, beta receptor, beta-1 selective, second generation treats HTN, CHD, angina, no intrinsic sympathetic activity and membrane stabilization activity |
|
bisoprolol* |
adrenergic antagonist, beta receptor, beta-1 selective, second generation treats HTN, has better beta-1 selectivity than other drugs besides nebivolol so better for COPD (check?), no intrinsic sympathetic activity and membrane stabilization activity |
|
esmolol* |
adrenergic antagonist, beta receptor, beta-1 selective, second generation treat critically ill pt (given IV) with need for rapid onset and short duration, watch out for bradycardia, heart failure, hypotension, no intrinsic sympathetic activity and membrane stabilization activity |
|
metoprolol* |
adrenergic antagonist, beta receptor, beta-1 selective, second generation treats essential HTN, preventing MI, adjunct for hyperthyroidism, migraine, no intrinsic sympathetic activity or membrane stabilization |
|
carteolol* |
adrenergic antagonist, beta receptor, non-selective, third generation beta-2 agonist properties |
|
carvedilol* |
adrenergic antagonist, beta receptor, non-selective, third generation alpha-1 adrenergic receptor blockade Ca2+ entry blockade antioxidant and anti-inflammatory action |
|
bucindolol |
adrenergic antagonist, beta receptor, non-selective, third generation |
|
labetalol* |
adrenergic antagonist, beta receptor, non-selective, third generation alpha-1 adrenergic receptor blockade |
|
betaxolol* |
adrenergic antagonist, beta receptor, beta-1 selective, third generation treats HTN, angina, glaucoma (reduces production of aqueous humor), slight membrane stabilization activity |
|
celiprolol* |
adrenergic antagonist, beta receptor, beta-1 selective, third generation increased production of NO beta-2 agonist properties |
|
nebivolol* |
adrenergic antagonist, beta receptor, beta-1 selective, third generation increased production of NO |
|
nipradolol* |
increased production of NO |
|
tilisolol* |
opening of K+ channels |
|
phenylephrine |
adrenergic agonist, direct acting, selective, alpha-1 |
|
metaraminol |
adrenergic agonist, direct acting, selective, alpha-1 rapid |
|
midodrine |
adrenergic agonist, direct acting, selective, alpha-1 prodrug, do not give to elderly |
|
clonidine |
adrenergic agonist, direct acting, selective, alpha-2 |
|
apraclonidine |
adrenergic agonist, direct acting, selective, alpha-2 |
|
brimonidine |
adrenergic agonist, direct acting, selective, alpha-2 |
|
guanabenz |
adrenergic agonist, direct acting, selective, alpha-2 |
|
tizanidine |
adrenergic agonist, direct acting, selective, alpha-2 |
|
dobutamine |
adrenergic agonist, direct acting, selective, beta-1 |
|
terbutaline |
adrenergic agonist, direct acting, selective, beta-2 SABA |
|
albuterol |
adrenergic agonist, direct acting, selective, beta-2 SABA |
|
salmeterol |
adrenergic agonist, direct acting, selective, beta-2 LABA |
|
formoterol |
adrenergic agonist, direct acting, selective, beta-2 LABA |
|
epinephrine |
adrenergic agonist, direct acting, non-selective, alpha-1,2, beta-1,2 greater affinity for beta-2 |
|
norepinephrine |
adrenergic agonist, direct acting, non-selective, alpha-1,2, beta-1 greater affinity for alpha-1,2, beta-1 |
|
isoproterenol |
adrenergic agonist, direct acting, non-selective, beta-1,2 |
|
alpha-1 adrenergic receptor blockade drugs |
labetalol, carvedilol |
|
increased production of NO drugs |
celiprolol, nebivolol, nipradolol |
|
beta-2 agonist properties |
celiprolol, carteolol |
|
Ca2+ entry blockade |
carvedilol |
|
opening of K+ channels |
tilisolol |
|
antioxidant and anti-inflammatory action |
carvedilol |