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NMDA receptor antagonist --> prevents excitotoxicity (cell death!!) from too much glutamate in Alzheimer's |
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achetylcholinesterase inhibitor Alzheimer's |
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achetylcholinesterase inhibitor Alzheimer's |
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achetylcholinesterase inhibitor Alzheimer's |
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inhibits ability to store NE, A, 5-HT --> amine depletion Huntington's |
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promotes early degradation of DA --> amine depletion Huntington's |
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5-HT1B/1D agnoist coronary vasospasm -- not for CAD or Prinzmetal's angina |
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binds Ca2+ channels --> decreased glutamate/NE release neuropathic pain, fibromyalgia, partial seizures |
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Definition
ergot, dopamine receptor agonist |
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non-ergot, dopamine receptor agonist |
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non-ergot, dopamine receptor agonist |
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increase DA release (increase endogenous DA effect) |
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COMT inhibitor -- inhibit peripheral methylation --> more DA available centrally |
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Definition
COMT inhibitor -- inhibit peripheral AND central methylation --> more DA available centrally |
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antimuscarinic helps tremor/rigidity |
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alpha-agonist decrease aqueous humor secretion (2/2 vasoconstriction) mydriasis (NOT for closed-angle glaucoma!!), stinging |
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Definition
alpha-agonist decrease aqueous humor secretion no eye changes |
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timolol, betaxolol, carteolol |
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Definition
beta-blockers carteolol is non-selective (breaks A-->M rule!!) decrease aqueous humor secretion no eye changes |
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Definition
alpha-agonist decrease aqueous humor secretion (2/2 decreased HCO3) no eye changes |
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Definition
direct cholinomimetic increase outflow of aqueous humor, contract ciliary muscle and open traecular meshwork; use in emergencies!! miosis, cyclospasm |
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Definition
direct cholinomimetic increase outflow of aqueous humor, contract ciliary muscle and open trabecular meshwork miosis, cyclospasm |
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Definition
indirect cholinomimetic increase outflow of aqueous humor, contract ciliary muscle and open trabecular meshwork miosis, cyclospasm |
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Definition
indirect cholinomimetic increase outflow of aqueous humor, contract ciliary muscle and open trabecular meshwork miosis, cyclospasm |
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Definition
PGF2alpha indirect cholinomimetic increase outflow of aqueous humor darkens color of iris!! |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission for cough |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission for diarrhea |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission for diarrhea |
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Definition
opioid receptor agonists -- open K+ channels, close Ca2+ channels --> decrease synaptic transmission |
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Definition
acute pulm edema (decrease anxiety and preload) |
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Definition
partial agonist --> can cause withdrawal |
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Definition
very weak opioid agonist inhibits 5-HT and NE reuptake decreases seizure threshold |
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mixed agonist-antagonist --> can cause withdrawal |
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Definition
mu -- endorphins delta -- enkephalin kappa -- dynorphin |
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Definition
increase Na+ channel inactivation, inhibit glutamate release nystagmus/ataxia, SLE-like syndrome, gingival hyperplasia in kids, peripheral neuropathy, hirsutism, megaloblastic anemia, fetal hydantoin syndrome, generalized LAD (pseudolymphoma!!) first line for status prophylaxis |
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Definition
increase Na+ channel inactivation for trigeminal neuralgia blood stuff (agranulocytosiss, aplastic anemia), liver toxicity, Stevens-Johnson, SIADH |
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blocks voltage-gated Na+ channels Steven-Johnson |
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Definition
GABA analog, but really inhibits HVA Ca2+ channels for peripheral neuropathy, postherpetic neuralgia |
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Definition
blocks Na+ channels, increase GABA action |
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Definition
increase duration of Cl channel opening (GABA-A) for pregnant women, children contraindicated in porphyria |
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Definition
increase Na+ channel inactivation, increase GABA concentration for myoclonic seizures hepatotoxicity, neural tube defects |
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Definition
blocks thalamic T-type Ca2+ channels EFGH -- Ethosuximide, Fatigue, GI, Headache + Stevens-Johnson |
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Definition
increase frequency of Cl- channel opening (GABA-A)
don't take with barbituates, alcohol, neuroleptics, 1st gen antihistamines
short -- TOM = Triazolam, Oxazepam, Midazolam, + alprazolam intermediate -- chlordiazepoxide, prazepam, clonazepam, flurazepam, diazepam long -- LET = lorazepam, estazolam, temazepam |
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Definition
inhibits GABA reuptake partial seizures ONLY |
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Definition
irreversibly inhibits GABA transaminase partial seizures ONLY |
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Definition
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Definition
increase duration of Cl channel opening (GABA-A) contraindicated in porphyria |
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Definition
increase duration of Cl channel opening (GABA-A) high lipid solubility, rapid entry into brain, rapid redistribution into skeletal muscles and fat --> rapid recovery |
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Definition
increase duration of Cl channel opening (GABA-A) contraindicated in porphyria |
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Definition
non-benzo hypnotics, less dependence act at BZ1 receptor |
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Definition
non-benzo hypnotics, less dependence act at BZ1 receptor |
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Definition
non-benzo hypnotics, less dependence act at BZ1 receptor |
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Term
anesthetics -- solubility in blood -- solubility in lipids -- gas tension -- AV concentration gradient |
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Definition
-- high blood solubility, slower onset and recovery -- high lipid solubility, high potency, low MAC -- high gas tension, high RR, deep ventilation -- high AV concentration gradient, slower onset of action |
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Definition
inhaled anesthetic high lipid and blood solubility myocardial depression (hypotension, decreased renal perfusion), resp depression, increased cerebral blood flow (can cause cerebral edema!!) hepatic necrosis (rapid death, high AST/ALT, PT, WBC, eosinophils, normal albumin -- t1/2 = 20d), arrhythmias |
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Definition
inhaled anesthetic seizures |
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Definition
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Definition
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inhaled anesthetic nephrotoxic |
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Definition
inhaled anesthetic low lipid and blood solubility |
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Definition
arylcyclohexylamine (PCP analogs) block NMDA (glutamate) receptors cardiovascular stimulants!! |
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Definition
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esters -- allergic reactions, shorter duration of action amides -- 2 I's!! |
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local anesthetics (-caine) |
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Definition
-- block inside of activated Na+ channels -- acidic tissue (infection), alkaline anesthetics are changed and cannot penetrate membrane --> need higher dose -- small myelinated, then small unmyelinated, large myelinated, finally large unmyelinated -- lose pain, then temp, touch, finally pressure -- except for cocaine, given with epi (NOT nose, digits, penis, pinna) |
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Definition
depolarizing neuromuscular blocking agent Phase I -- prolonged depolarization (fasciculations), no antidote Phase II -- repolarized but blocked, antidote is cholinesterase inhibitors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
non-depolarizing neuromuscular blocking drugs competitively blocks ACh receptors |
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Definition
prevents Ca2+ release from sarcoplasmic reticulum for malignnt hyperthermia and meuroleptic malignant syndrome |
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Definition
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random thing about levodopa |
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Definition
B6 increases peripheral metabolism of levodopa --> decreased effectiveness!! |
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Definition
Train of Four
non-depolarizing neuromuscular blocking drugs |
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Definition
Train of Four
depolarizing neuromuscular blocking drugs
Note: usually succinylcholine lasts ~10min, but some people have atypicalcholinesterase and it takes hours!! (give antidote during Phase II!!) |
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random opioid side effect |
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Definition
biliary colic -- SM contraction of sphincter of Oddi --> increased GB pressure |
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