Exam 4 - Hallucinogens Flashcards

1
Q

In the early use of hallucinogens, what were they mainly used for? Where could they be found?

A
  • often used in religious ceremonies, used to predict the future
  • found in wide variety of plants like iboga plant, psilocybin mushroom, peyote cactus
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2
Q

When was LSD discovered?

A

by Albert Hofmann in 1938

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3
Q

What are the pharmacokinetics of LSD?

A
  • peak plasma levels reached in 2 hours
  • rapidly absorbed and crosses BBB
  • half life ranges btwn 2-3 hours, and can last up to 12
  • extremely potent, but has no confirmed LD
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4
Q

What are the pharmacodynamics of LSD?

A
  • partial serotonin agonist, creates sensory overload due to concentrations in prefrontal area, somatosensory areas, brain stem, etc
  • hallucinogenic effects mediated by the 5-HT2A receptor
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5
Q

What are the effects of serotonergic hallucinogens?

A
  • activation of sympathetic nervous system
    • pupil dilation
    • increased HR and BP
    • increased temp and sweating
  • magical thinking
  • mood interferences
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6
Q

What are the adverse effect of hallucinogens?

A
  • acute panic or paranoid reaction
  • hallucinogen persisting perception disorder (HPPD) - an element of the experience occurs a period of time later, flashback
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7
Q

MDMA

A
  • developed in 1914
  • similar effects of amphetamines by influencing serotonin (depletes) and dopamine transmission
  • produces no or few visual hallucinations
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8
Q

What are the somatic effects of MDMA?

A
  • dramatic increase in BP and temp
  • sympathomimetic
  • jaw clenching, suppressed appetite, restlessness, insomnia, impaired gait, restless legs, convulsions
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9
Q

What are the adverse effects of MDMA?

A
  • lack of energy/fatigue, difficulty concentrating
  • can lead to death or kidney failure
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10
Q

Neurotoxicity of MDMA

A
  • can damage serotonin and dopamine axon terminals
  • damage can continue up to 2 years after cessation
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11
Q

MDMA psychiatric problems

A
  • withdrawal can cause depression
  • impairments in memory, both verbal and visual
  • impairments in decision making
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12
Q

Dissociative anesthetic hallucinogens

A
  • PCP and ketamine
  • awake but not cognisant
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13
Q

Pharmacokinetics of PCP and ketamine

A
  • antagonist for glutamate/NMDA receptors
  • remains unmetabolized for more than 2 days, detectable in urine for several weeks
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14
Q

Effects of PCP

A
  • altered body image (depersonalization)
  • aloneness/isolation
  • cognitive disorganization
  • drowsiness and apathy
  • negativism/hostility
  • euphoria/inebriation
  • hypnagogic (dreamlike) states
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15
Q

PCP intoxication - Acute brain syndrome

A
  • disorientation, confusion, poor judgement, abstract/absence of thought
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16
Q

PCP intoxication - Catatonic syndrome

A

rigidity or catalepsy, psychosocial withdrawal, excitement (agitation, violence)

17
Q

PCP intoxication - Toxic psychosis

A

hallucinations and/or delusions, w/ or w/o acute brain syndrome

18
Q

PCP intoxication - Coma

A

periods of coma that can last more than a day