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Ethanol-like effects of thiopental and ketamine in healthy humans

D. Dickerson, Brian Pittman, E. Ralevski, A. Perrino, D. Limoncelli, J. Edgecombe, G. Acampora, JH Krystal, Ismene L. Petrakis

Journal of Psychopharmacology February 1, 2010 DOI: 10.1177/0269881108098612 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Peer reviewed
Sample size 28
Population Healthy adults aged 21-30 with no personal or family histories of alcoholism
Interventions Thiopental Ketamine
Topics Esketamine Ketamine
Key findings Both thiopental and ketamine produced significant ethanol-like effects and subjective intoxication, but ketamine's effects were more intense and included perceptual alterations not seen with thiopental. The authors propose that GABA-A receptor facilitation contributes to social drinking effects, while NMDA antagonism contributes more to intoxication features.

Abstract

The γ-aminobutyric acid-A (GABA A ) and N-methyl-D-aspartate (NMDA) receptors mediate aspects of the behavioural effects of alcohol. Prior studies reported drugs that block NMDA receptors or facilitate GABA A receptor function produce ethanol-like effects in humans. The purpose of this study was to compare the ethanol-related effects of two pharmacological agents with known NMDA and GABA A receptor activity. As part of an ongoing, larger study, 28 subjects (age, 21—30) with no personal or family histories of alcoholism were administered subanesthetic doses of the GABA A receptor agonist thiopental, the NMDA receptor antagonist, ketamine and placebo on three separate test days. Various ethanol-related measures were administered. At doses of thiopental and ketamine that produced similar levels of sedation and cognitive effects, both agents produced significant ethanol-like effects and subjective intoxication. However, the intensity of the ethanol-like effects of ketamine was greater than that of thiopental. In addition, ketamine produced alterations in perception that were not produced by thiopental. These data provide further support for a model where GABA A receptor facilitation may contribute significantly to ethanol effects associated with social drinking, whereas NMDA receptor antagonism may contribute to relatively greater extent to features of ethanol ‘intoxication’.

Comparable studies

Other randomized controlled trials on ketamine, most cited first.

Study Year Design Participants
Subanesthetic Effects of the Noncompetitive NMDA Antagonist, Ketamine, in Humans Healthy human subjects recruited from the community 1994 Randomized controlled trial n = 19
Antidepressant Efficacy of Ketamine in Treatment-Resistant Major Depression: A Two-Site Randomized Controlled Trial Patients with treatment-resistant major depression experiencing a major depressive episode 2013 Randomized controlled trial n = 73
Remifentanil-induced Postoperative Hyperalgesia and Its Prevention with Small-dose Ketamine Patients undergoing major abdominal surgery 2005 Randomized controlled trial n = 75
Efficacy of Intravenous Ketamine for Treatment of Chronic Posttraumatic Stress Disorder Patients with chronic PTSD related to a range of trauma exposures 2014 Randomized controlled trial n = 41
Ketamine-Induced Deficits in Auditory and Visual Context-Dependent Processing in Healthy Volunteers Healthy volunteers 2000 Single-blind placebo-controlled study n = 20

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