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Pharmacologic Similarities and Differences Among Hallucinogens

Kristin Waters

The Journal of Clinical Pharmacology August 1, 2021 DOI: 10.1002/jcph.1917 (opens in new tab)

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AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics LSD Psilocybin Serotonin
Keywords Hallucinogen Pharmacology Dopamine
Citations 18
Key findings Hallucinogens vary in their mechanisms of action, with classical serotonergic hallucinogens differing from those acting via NMDA antagonism, opioid agonism, or monoamine reuptake inhibition, and this pharmacologic diversity influences their physical and psychiatric effects and toxicities.

Abstract

Abstract Hallucinogens constitute a unique class of substances that cause changes in the user's thoughts, perceptions, and mood through various mechanisms of action. Although the serotonergic hallucinogens such as lysergic acid diethylamide, psilocybin, and N,N‐ dimethyltryptamine have been termed the classical hallucinogens , many hallucinogens elicit their actions through other mechanisms such as N‐methyl‐D‐aspartate receptor antagonism, opioid receptor agonism, or inhibition of the reuptake of monoamines including serotonin, norepinephrine, and dopamine. The aim of this article is to compare the pharmacologic similarities and differences among substances within the hallucinogen class and their impact on physical and psychiatric effects. Potential toxicities, including life‐threatening and long‐term effects, will be reviewed.

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