Pharmacology Flashcards

1
Q

1) THC metabolism
2) drugs that increase THC effect

A

1) CYP2C19, CYP3A4, CYP2C9
2) fluoxetine, ketoconazole

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2
Q

BZD mechanism of action

A

facilitates inhibition at GABA-A receptors

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3
Q

CYP2D6 plays a role in what opiate/opioid metabolism?

A

1) codeine –> morphine
2) hydrocodone –> hydromorphone
3) oxycodone –>oxymorphone
4) noroxycodone –> noroxymorphone

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4
Q

Ketamine mechanisms of action

A

mainly non-competitive antagonist at NMDA glutamate receptor

also
- antagonist at muscarinic and nicotinic acetylcholine receptors
- block sodium and potassium channels
- activate high-affinity D2 dopamine receptors and L-type voltage gated calcium channels
- facilitate GABA inhibition

ultimately INCREASE DOPAMINE, NE, and SEROTONIN in brain

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5
Q

buspirone MOA

A

partial agonist at serotonin 5-HT1a

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6
Q

disulfiram

A

1) blocks dopamine beta hydroxylase in brain
2) irreversibly binds/blocks alcetaldehyde dehydrogenase

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7
Q

pregabalin

A

calcium channel antagonist

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8
Q

1) baclofen
2) carisoprodol

A

1) GABA-B agonist
2) GABA-A activity (like BZD)

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9
Q

acamprosate

A

antagonist of glutaminergic activity at NMDA receptros

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10
Q

naltrexone

A

mu opioid receptor antagonist

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11
Q

MAOI inhibitor

A

selegine

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12
Q

bupropion

A

block uptake of NE and dopamine, some action on nicotinic and serotonergic receptors

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13
Q

SSRI

A

block serotonin reuptake (5-HT)

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14
Q

mirtazapine

A

antagonism at H1 and alpha -1 receptors

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15
Q

phencyclidine

A

1A) noncompetitive NMDA receptor antagonist;
1B) (ant at NMDA glutamate receptor)
2) also inhibits reuptake of dopamine, NE, and 5-HT

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16
Q

Dissociatives MOA:
PCP, ketamine, detromethorphan (DXM)

A

noncompetitive NMDA receptor antagonist
(dissociatives, subclass of hallucinogens)

17
Q

Cocaine (A) and Amphetamine (B) MOA

A

1A) Cocaine: DOPAMINE transporter reuptake inhibitor
1B) amphetamine: DOPAMINE stimulation
2) increase circulation of corticotropin-releasing factor (CRF) and nuropeptide Y (NPY) throughout brain regions affecting entire addiction pathway

18
Q

barbituates (ex phenobarbital)

A

1) enhance inhibitory control of GABA-A (like bzd, except bzds increase freq of calcium channel opening, and barbs increase duration of ca channel opening)
2) decrease glutamate excitation by decreasing ampa and kainate activity

19
Q

MDMA
onset
peak
1/2 life
time to 95% clearance

A

MDMA onset 20m - 1h, peak 2h, 1/2 life 8 hours, 40h and 5 1/2 lives to 95% clearance

20
Q

haloperidol

A

dopamine D2 antagonist antipsychotic
helpful in etoh psychosis

21
Q

EtOH MOA

A

1) GABAa receptor up
2) inhibit NMDA glutamate receptor function

22
Q

nicotine MOA

A

agonist at nicotine acetylcholine receptors

23
Q

cannabinoids MOA

A

agonist at CB1 (brain) and CB2 (immune) cannabinoid receptors

24
Q

opioid MOA

A

agonism at mu, kappa, and delta opioid receptors

25
Q

A) hallucinogens MOA: LSD, MDMA, psilocybin, mescaline, DMT
B) hallucinogen outlier salvia MOA

A

A) partial agonist at 5-HT3, 5-HT2 serotonin receptors