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The effect of optical isomers of 3,4-methylenedioxymethamphetamine (MDMA) on stereotyped behavior in rats.

M Hiramatsu, Toshitaka Nabeshima, T Kameyama, Y Maeda, A K Cho

Pharmacology, Biochemistry, and Behavior June 1989 DOI: 10.1016/0091-3057(89)90511-x (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Peer reviewed
Interventions S(+)-MDMA R(-)-MDMA p-chloroamphetamine
Topics MDMA
Key points S(+)-MDMA was more potent than R(-)-MDMA in eliciting stereotyped behaviors including sniffing, head-weaving, backpedalling, turning, and wet-dog shakes, consistent with the S(+) enantiomer's greater potency in releasing neurotransmitters. S(+)-MDA, the desmethyl derivative, was more potent than S(+)-MDMA and produced wet-dog shake behavior.

Abstract

The relative potencies of S(+)-, R(-)-3,4-methylenedioxymethamphetamine (MDMA) and S(+)-methylene-dioxyamphetamine (MDA) in inducing stereotyped behavior were determined in comparison with p-chloroamphetamine. S(+)-MDMA was more potent than R(-)-MDMA in eliciting stereotyped behaviors such as sniffing, head-weaving, backpedalling and turning and wet-dog shakes. These results are consistent with the actions of the drug on release of neurotransmitters in which the S(+) enantiomer is more potent. The desmethyl derivative of (+)MDMA, (+)MDA, was more potent than (+)MDMA in eliciting stereotyped behaviors, and produced wet-dog shake behavior.

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