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Mahmoud M. Iravani

Queen Mary University of London

2 papers in the library · 161 citations · publishing 2000-2003

Papers

3,4-Methylenedioxymethamphetamine (Ecstasy) Inhibits Dyskinesia Expression and Normalizes Motor Activity in 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Treated Primates

Journal of Neuroscience October 8, 2003 Mahmoud M. Iravani, Michael S. Jackson, Mikko Kuoppamäki et al. 105 citations

MDMA (ecstasy) reduced dyskinesia and extended the effect of L-DOPA in a single Parkinson's disease patient. In MPTP-treated marmosets primed with L-DOPA, MDMA given alone transiently relieved motor disability but worsened symptoms over 60 minutes. When combined with L-DOPA, MDMA markedly decreased dyskinesia by reducing chorea and, to a lesser extent, dystonia, and lowered locomotor activity to normal levels. MDMA also alleviated dyskinesia induced by the dopamine D2/3 agonist pramipexole. These effects were fully blocked by the serotonin reuptake inhibitor fluvoxamine and partially inhibited by 5-HT1a/b antagonists, indicating MDMA's antidyskinetic action is mediated through serotonin systems.

Direct effects of 3,4‐methylenedioxymethamphetamine (MDMA) on serotonin or dopamine release and uptake in the caudate putamen, nucleus accumbens, substantia nigra pars reticulata, and the dorsal raphé nucleus slices

Synapse April 27, 2000 Mahmoud M. Iravani, Daniel Asari, Jyoti C. Patel et al. 56 citations

MDMA does not directly cause the release of serotonin or dopamine in brain slices from rats, contrary to some earlier assumptions. Instead, it acts as a potent inhibitor of the reuptake of both neurotransmitters, slowing their removal from the synapse. MDMA also potentiated electrically stimulated serotonin release in the substantia nigra pars reticulata and dopamine release in the caudate putamen, but had no effect on stimulated release in the dorsal raphé nucleus or nucleus accumbens. These findings clarify MDMA's mechanism of action as distinct from that of amphetamine.