Moa Flashcards

0
Q

Competitive antagonist of BZD at GABAa receptor

A

Flumazenil

ALT: doxopram, nicetamide

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1
Q

Has a GABA mimetic activity by acting in the BZD receptor at GABA receptor CI complex, thus prolonging the inhibitory effects of GABA

A

Benzodiazepines

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2
Q

Enhance GABA’s acxn by binding to a different site on the GABA receptor-chloride channel, but less specific than BZD

A

Barbiturates

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3
Q

Partial agonist at brain 5-HT1a receptor

A

Buspirone

For generalized anxiety stage

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4
Q

Not a BZD but act on the same site as BZD

A

Zolpidem

-pure hynotic acxn

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5
Q

Enhances GABA at GABAa receptor,
Inhibits the ability of glutamate to open the cation channel assoc w/ NMDA(N-methyl-D-Aspartate) subtype of glutamate receptor

A

Alcohol

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6
Q

H1 receptor antagonist

A

Antihistamine

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7
Q

Inhibition of phosphodiesterase thus inc cAMP; inc Ca permeability; blocks adenosine receptors

A

Methylxanthines

+ chrono and inotropic effects on heart

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8
Q

Stops MAO, inc rel. of NE

A

Amphetamines

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9
Q

Has the ability to to have vasoconstriction by itself; potentiates and prolongs CNS and peripheral acxns of cathecolamine

A

Cocaine

-intense euphoria

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10
Q

Inhibits reuptake of DOPA, SE and NE

A

PCP “angel dust”

-Analog of ketamine

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11
Q

Interacts w/ several 5HT receptor subtypes in the brain

A

LSD

-w brilliant color SE

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12
Q

Inc reuptake of Ne into adrenergic nerve endings and dec the rel of NE; alters cellular conc of IP3

A

Lithium

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13
Q

Activate the myocardial beta1 receptor and thus inc the force of contraction of the failing heart; inc CO

A

Dopamine and dobutamine

Used in CHF

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14
Q

Displace NE from presynaptic terminals and bind to adrenergic receptors

A

Mixes sympathomimetics

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15
Q

Decreases catecholamine release (reuptake to the vesicles then replace NE)

A

Guanethidine

16
Q

Depletes catecholamines

A

Reserpine

17
Q

Competitive cholinesterase antagonist

A

Edrophonium

18
Q

Compete w/ Ach for the active site of the enzyme

A

Carbamates

19
Q

Have a high affinity for the active site of the enzyme (cholinesterase inh)

A

OrganoPO4

20
Q

Block nicotinic receptors both in the sympathetic and parasympathetic ganglia

A

Ganglionic blockers

22
Q

Inhibits uptake and release of NE from brain synapse but does not influence GABA uptake; blocks Na channels in the brain, also potentiates acxn of GABA

A

Carbamazepine

23
Q

potentiates the inhibitory acxn effects of GABA; blocks excitatory responses induced by glutamate

A

phenobarbital

24
Q

inactivates Na channels (anticonv)

A

lamotrigine

25
Q

has a weak effects on Na channels and little effect on GABA

A

Felbamate

26
Q

similar to carbamazepine and phenytoin; potentiates inh effect of GABA by acting at different receptor from BZD or barbi site

A

topiramate

27
Q

inhibits GABA uptake

A

tiagabine

28
Q

inhibits GABA-T in the brain

A

valproic acid

29
Q

reduce T-type Ca currents in thalamic neurons

A

oxazolidinediones

30
Q

most effective in status epilepticus

A

diazepam

31
Q

also used in status epilepticus

A

alprazolam

32
Q

used in absence seizure, infantile spasm, myoclonic seizure, and atonic seizure

A

clonazepam

33
Q

adjunct medication in comples partial seizure

A

clorazepate

34
Q

used in infantile spasm aand myoclonic seizure

A

nitrazepam

35
Q

diminish the depolarizing acxn of bicarbonate ions moving out of neurons via GABA receptor ion channel

A

acetazolamide