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Prepulse inhibition of the startle reflex and its attentional modulation in the human S-ketamine and N,N-dimethyltryptamine (DMT) models of psychosis

Karsten Heekeren, Anna Neukirch, Jörg Daumann, Martina Stoll, Maja Obradovic, K.‐a. Kovar, Mark A. Geyer, Euphrosyne Gouzoulis‐mayfrank

Journal of Psychopharmacology May 1, 2007 DOI: 10.1177/0269881107077734 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Double-blind crossover study Peer reviewed
Sample size 15
Population Healthy volunteers
Interventions S-ketamine N N-dimethyltryptamine (DMT)
Topics Ketamine LSD Mescaline Psilocybin Serotonin Esketamine 5-MeO-DMT DMT
Keywords Hallucinogen Prepulse inhibition Moro reflex Psychosis Schizophrenia object-oriented programming Phencyclidine Startle response Habituation Startle reaction Nmda receptor
Citations 49
Key points S-ketamine increased PPI and decreased startle magnitude, while DMT had no significant effect on PPI, and neither drug attenuated PPI as seen in schizophrenia.

Abstract

Patients with schizophrenia exhibit diminished prepuLse inhibition (PPI) of the acoustic startle reflex and deficits in the attentional moduLation of PPI. Pharmacological challenges with hallucinogens are used as models for psychosis in both humans and animals. RemarkabLy, in contrast to the findings in schizophrenic patients and in animal hallucinogen modeLs of psychosis, previous studies with healthy volunteers demonstrated increased levels of PPI after administration of low to moderate doses of either the antiglutamatergic hallucinogen ketamine or the serotonergic hallucinogen psilocybin. The aim of the present study was to investigate the influence of moderate and high doses of the serotonergic hallucinogen N,N-dimethyltryptamine (DMT) and the N-methyl-D-aspartate antagonist S-ketamine on PPI and its attentional modulation in humans. Fifteen healthy volunteers were included in a double-blind cross-over study with two doses of DMT and S-ketamine. Effects on PPI and its attentional modulation were investigated. Nine subjects completed both experimental days with the two doses of both drugs. S-ketamine increased PPI in both dosages, whereas DMT had no significant effects on PPI. S-ketamine decreased and DMT tended to decrease startle magnitude. There were no significant effects of either drug on the attentional modulation of PPI. In human experimental hallucinogen psychoses, and even with high, clearly psychotogenic doses of DMT or S-ketamine, healthy subjects failed to exhibit the predicted attenuation of PPI. In contrast, PPI was augmented and the startle magnitude was decreased after S-ketamine. These data point to important differences between human hallucinogen models and both animal hallucinogen models of psychosis and naturally occurring schizophrenia.

Comparable studies

Other randomized controlled trials on 5-MeO-DMT, most cited first.

Study Year Design Participants
Dose-Response Study of N,N-Dimethyltryptamine in Humans Experienced hallucinogen users 1994 Double-blind, saline placebo-controlled, randomized study n = 12
Psychological Effects of (S)-Ketamine and N,N-Dimethyltryptamine (DMT): A Double-Blind, Cross-Over Study in Healthy Volunteers Healthy volunteers 2005 Double-blind crossover study n = 9
Differential tolerance to biological and subjective effects of four closely spaced doses of N,N-dimethyltryptamine in humans Experienced hallucinogen users 1996 Randomized controlled trial n = 13
Pharmacokinetics of N,N-dimethyltryptamine in Humans. Healthy adults 2023 Phase I component of a phase I/IIa randomised, double-blind, placebo-controlled, parallel-group, dose-escalation trial n = 24
Phase 1, placebo-controlled, single ascending dose trial to evaluate the safety, pharmacokinetics and effect on altered states of consciousness of intranasal BPL-003 (5-methoxy-N,N-dimethyltryptamine benzoate) in healthy participants. Healthy psychedelic-naïve participants 2024 Double-blind, placebo-controlled single ascending dose study n = 44

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