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Brain mechanisms of hallucinogens and entactogens

Franz X. Vollenweider

Dialogues in Clinical Neuroscience December 31, 2001 DOI: 10.31887/dcns.2001.3.4/fxvollenweider (opens in new tab)

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AI-extracted from the abstract
Characteristics Review Peer reviewed
Population Humans and rats
Topics MDMA Mescaline Psilocybin Serotonin
Keywords Hallucinogen Psychotomimetic Thalamus Amygdala Sensory gating Prefrontal cortex
Citations 127
Key findings Classic hallucinogens and dissociative anesthetics produce overlapping psychotic syndromes and disrupt sensory gating via a common pathway involving cortico-striato-thalamic circuitry, while MDMA produces a distinct emotional state with different brain activation patterns.

Abstract

This review focuses on recent brain imaging and behavioral studies of sensory gating functions, which assess similarities between the effects of classic hallucinogens (eg, psilocybin), dissociative anesthetics (eg, ketamine), and entactogens (eg, 3,4-methylenedioxymethamphetamine [MDMA]) in humans. Serotonergic hallucinogens and psychotomimetic anesthetics produce overlapping psychotic syndromes associated with a marked activation of the prefrontal cortex (hyperfrontality) and other overlapping changes in temporoparietal, striatal, and thalamic regions, suggesting that both classes of drugs act upon a common final pathway. Together with the observation that both hallucinogens and N-methyl-oaspartate (NMDA) antagonists disrupt sensory gating in rats by acting on 5-hydroxytryptamine (serotonin) 5-HT(2) receptors located in cortico-striato-thalamic circuitry these findings suggest that disruption of cortico-subcortical processing leading to sensory overload of the cortex is a communality of these psychoses. In contrast to hallucinogens, the entactogen MDMA produces an emotional state of positive mood, concomitant with an activation of prefrontolimbiclparalimbic structures and a deactivation of amygdala and thalamus.

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