Psychological effects of MDE in normal subjects. Are entactogens a new class of psychoactive agents?
L Hermle, M Spitzer, D Borchardt, K A Kovar, E Gouzoulis
Neuropsychopharmacology February 1993 DOI: 10.1038/npp.1993.19 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Double-blind placebo-controlled psychometric study Peer reviewed |
|---|---|
| Sample size | 14 |
| Population | Healthy normal control volunteers (8 male in the first study; 3 male and 3 female in the second) |
| Dose | 140 mg |
| Duration | Testing at -1, +2, +5, +24 hours and +7 days in the first study; -1, +8.5, +24 hours and +7 days in the second |
| Key points | MDE (140 mg) produced a partially controllable state of enhanced insight, empathy, and peaceful feelings along with stimulation, increased psychomotor drive, talkativeness, and facilitated communication, resembling prior anecdotal reports of MDMA/MDE. Adverse effects included one toxic psychosis, one dysphoric reaction, and one volunteer with anxiety episodes for several days. The authors state the findings support the hypothesis that MDMA and MDE represent a novel pharmacologic class. |
Abstract
The so-called entactogens 3,4-methylenedioxymethamphetamine ([MDMA] also known as "Ecstasy," or "Adam") and its analog 3,4-methylenedioxyethamphetamine ([MDE] also known as "Eve") exert similar psychotropic effects in humans. Two double-blind placebo-controlled psychometric studies with normal control subjects were conducted. Placebo or MDE (140 mg) was administered orally to eight male volunteers at 1:30 P.M. and to six subjects (3 male, 3 female) at 11 P.M. Psychologic tests and clinical ratings were performed 1 hour before the administration of the drugs, as well as 2, 5, and 24 hours after drug intake and 7 days thereafter in the first study. In the second study, measures were taken at times -1, +8.5, +24 hours, and +7 days. The majority of the psychotropic effects resembled those that have already been described in anecdotal reports. The substance produced a partially controllable state of enhanced insight, empathy, and peaceful feelings. All subjects displayed a general stimulation with increased psychomotor drive, logorrhea, and facilitation of communication. One of the fourteen volunteers developed a toxic psychosis. One volunteer displayed a dysphoric reaction, one suffered from episodes of anxiety for some days after the experiment. The findings support the hypothesis that MDMA and MDE represent a novel pharmacologic class.
Citations in the library
Cited by 39
- Gender differences in the subjective effects of MDMA Psychopharmacology March 5, 2001
- Human psychopharmacology of Ecstasy (MDMA): a review of 15 years of empirical research Human Psychopharmacology: Clinical and Experimental December 1, 2001
- Human Pharmacology of 3,4-Methylenedioxymeth-amphetamine ("Ecstasy"): Psychomotor Performance and Subjective Effects Journal of Clinical Psychopharmacology August 1, 2000
- Neurometabolic Effects of Psilocybin, 3,4-Methylenedioxyethylamphetamine (MDE) and d-Methamphetamine in Healthy Volunteers A Double-Blind, Placebo-Controlled PET Study with [18F]FDG Neuropsychopharmacology June 1, 1999
- MDMA-Assisted Psychotherapy Using Low Doses in a Small Sample of Women with Chronic Posttraumatic Stress Disorder Journal of Psychoactive Drugs September 1, 2008
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Cites 8
- Differences Between the Mechanism of Action of MDMA, MBDB, and the Classic Hallucinogens. Identification of a New Therapeutic Class: Entactogens Journal of Psychoactive Drugs October 1, 1986
- Subjective Reports of the Effects of MDMA in a Clinical Setting Journal of Psychoactive Drugs October 1, 1986
- 'Eve' and 'Ecstasy'. A report of five deaths associated with the use of MDEA and MDMA JAMA March 27, 1987
- The Background and Chemistry of MDMA Journal of Psychoactive Drugs October 1, 1986
- Sleep EEG effects of 3,4-methylenedioxyethamphetamine (MDE; "eve") in healthy volunteers. Biological Psychiatry December 15, 1992
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