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The effect of MDA and MDMA ("Ecstasy") isomers in combination with pirenpirone on operant responding in mice.

John A. Rosecrans, Richard A Glennon

Pharmacology, Biochemistry, and Behavior September 1987 DOI: 10.1016/0091-3057(87)90008-6 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Peer reviewed
Sample size 27
Population Mice trained to bar-press for a liquid food reinforcement
Interventions R(-)-MDA S(+)-MDA S(+)-MDMA pirenpirone saline
Topics MDMA
Key findings Pirenpirone significantly attenuated the behaviorally disruptive effects of R(-)-MDA but not those of S(+)-MDA, R(-)-MDA, or S(+)-MDMA. The authors suggest that R(-)-MDA may produce its behavioral disruption via an action on 5-HT-2 receptors, consistent with prior research.

Abstract

The behaviorally disruptive effects of the optical isomers of 1-(3,4-methylenedioxyphenyl-2-aminopropane) (MDA) and its N-methyl derivative (MDMA) were evaluated in 27 mice trained to bar-press for a liquid food reinforcement. In addition, a second study was conducted in which mice were pretreated with either saline or the 5-HT-2 antagonist, pirenpirone, prior to the administration of either MDMA or MDA using the same behavioral procedure. The results indicated that the behaviorally disruptive effects produced only by R(-)-MDA, but not those of S(+)-MDA, R(-)-MDA, nor of S(+)-MDMA, were significantly attenuated by pirenpirone. These findings support previous research findings which indicate that this isomer may be producing its behaviorally disruptive effects via an action on 5-HT-2 receptors.

Comparable studies

Other preclinical and animal studies on MDMA, most cited first.

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