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Ecstasy counteracts catalepsy in rats, an anti-parkinsonian effect?

Werner J Schmidt, Andreas Mayerhofer, Anja Meyer, Karl-A Kovar

Neuroscience Letters September 27, 2002 DOI: 10.1016/s0304-3940(02)00823-6 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical animal study Peer reviewed
Population Rats with haloperidol-induced parkinsonism
Intervention 3
Topics MDMA
Key points 3,4-Methylenedioxymethamphetamine ('Ecstasy') dose-dependently and potently reversed haloperidol-induced parkinsonism in rats. The authors argue that a supraadditive effect of the enantiomers indicates both enantiomers contribute to the antiparkinsonian effects at two different target sites.

Abstract

Parkinson's disease is due to a dopamine deficiency caused by the degeneration of midbrain dopamine neurons. Current therapies are aimed to substitute dopamine or to directly stimulate postsynaptic dopamine receptors. However, not all patients profit from current therapies to the same extent, even serious side effects such as dyskinesias are complicating the therapy. Therefore, there is still a need for better anti-parkinsonian drugs. Here we show that some compounds from the 'Ecstasy'-derivatives exert potent anti-parkinsonian activity. 3,4-Methylenedioxymethamphetamine, 'Ecstasy' dose-dependently and very potently reversed haloperidol-induced parkinsonism in the rat. From the supraadditive effect of the enantiomers it may be concluded that both enantiomers contribute to the antiparkinsonian effects at two different target sites.

Comparable studies

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