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3,4-Methylenedioxyethylamphetamine (MDE), a novel analogue of MDMA, produces long-lasting depletion of serotonin in the rat brain.

George A. Ricaurte, K F Finnegan, D E Nichols, L E DeLanney, I Irwin, J W Langston

European Journal of Pharmacology June 4, 1987 DOI: 10.1016/0014-2999(87)90233-0 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Animal study Peer reviewed
Population Rats
Interventions 3 4-methylenedioxyethylamphetamine (MDE)
Topics MDMA Serotonin
Key points MDE produced a long-lasting, dose-related depletion of serotonin in rat brain, but did not reduce dopamine or norepinephrine levels on a long-term basis even at high doses. MDE was approximately one fourth as potent as MDMA at causing long-term serotonin depletion, suggesting it may be selectively toxic to central serotonergic neurons.

Abstract

The present study was carried out to asses possible toxic effects of 3,4-methylenedioxyethylamphetamine (MDE) on serotonergic, dopaminergic or noradrenergic neurons in the rat brain. It was found that MDE produced a long-lasting, dose-related depletion of serotonin (5HT). However, even at high dosage, MDE did not reduce the concentration of either dopamine (DA) or norepinephrine (NE) on a long-term basis. When compared to 3,4-methylenedioxymethylamphetamine (MDMA), MDE was approximately one fourth as potent as producing a long-term depletion of 5HT. These results suggest that MDE, like MDMA, may be selectively toxic to central serotonergic neurons.

Comparable studies

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

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