Drugs of Abuse Flashcards

1
Q
  • used and abused to increase wakefulness, attention, and physical performance, also anorexogenics
  • caffeine (adenosine antagonist), nicotine agonist (relaxation, increased alertness
A

stimulants

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2
Q

antidepressant used for smoking cessation

A

buproprion

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3
Q

nicotinic partial agonist, smoking cessation

A

varenicline

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4
Q
  • stimulate sympathetic nervous system, increase wakefulness and attention
  • pupil dilation, reinforcing euphoric effects and addictive potential due to stimulation of mesolimbic dopamine system
A

sympathomimetics/psychostimulants

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5
Q
  • inhibits dopamine reuptake, and norepi and serotonin
  • short duration of action
  • less associated with tolerance than other addictive drugs, but cravings strong
  • increases risk of intracranial hemorrhage, ischemic stroke, MI, arrhythmias, and seizures
  • used as topical local anesthetic for mucous membranes
A

cocaine

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6
Q
  • releases and blocks reuptake of dopamine, norepi, and serotonin
  • dopaminergic and serotonergic neurotoxin
  • tolerance can lead to dose escalation
  • long term use can lead to psychosis
  • withdrawal: dysphoria, drowsiness, insomnia, irritability
  • used for ADHD, narcolepsy, obesity
A

d-amphetamine

methamphetamine

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7
Q
  • amphetamine derivative w/ greater serotonergic activity (positive mood, empathy, extraversion, sensory awareness)
  • hallucinogenic effects
  • tolerance with repeated use
  • jaw clenching, tachy, muscle aches, hyperthermia, serotonin syndrome
  • withdrawal: depression, increased aggression
A

MDMA, ecstasy

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8
Q
  • alter cognition and perception (visual hallucinations, perceptual disturbances, intellectual insights, paranoia)
  • pupil dilation, nausea
  • increased glutamate release in cortex
  • rapid tolerance, no addiction
  • LSD, mescaline, psilocybin
A

psychedelic hallucinogens

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9
Q
  • feeling of disconnection from the body, hallucinations, emotional withdrawal, impaired memory
  • noncompetitive NMDA antagonist, binds specific site in NMDA receptor ion channel, acts at sigma site, no physiologic dependence
  • phencylcidine, ketamine
A

dissociative hallucinogens

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10
Q

phenycyclidine, ketamine

A

dissociative hallucinogens

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11
Q
  • euphoria, relaxation, giddiness
  • increased appetite, antiemetic
  • decrease intraocular pressure
  • dose dependent drowsiness and diminished coordination
  • stimulation of CNS receptor, immune modulation
A

cannabinoids

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12
Q

accumulates in adipose, detectable in urine for 3 weeks after cessation

A

THC

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13
Q

nonpsychoactive, anticonvulsant

A

cannabidiol

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14
Q
  • complete CNS depressant
  • decreases anxiety, removes inhibitions, lengthens reaction time
  • directly irritating to GI mucosa
  • vasodilation, decrease in BP
  • cirrhosis
  • crosses BBB and placenta
  • hepatic metabolism
A

ethanol

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15
Q
  • coma, hypothermia, decreased respiration, vomiting
  • hallucinosis, paranoid
  • withdrawal: seizures, tremors, treat w/ benzodiazepines
  • Wernicke Korsakoff due to thiamine deficiency
  • cirrhosis of liver
A

ethanol toxicity

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16
Q

inhibits conversion of acetaldehyde to acetate, causes toxicity (increased HR, dizziness, vomiting, unconsciousness)

A

disulfiram

17
Q
  • structural analog of homotaurine and GABA

- indicated for maintenance of abstinence from alcohol in patients who are abstinent at treatment initiation

A

acamprosate

18
Q

opioid antagonist, decreases cravings for ethanol and prevents relapse

A

naltrexone