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Science 6 September 1985:
Vol. 229. no. 4717, pp. 986 - 988
DOI: 10.1126/science.4023719

Articles

Science, Vol 229, Issue 4717, 986-988
Copyright © 1985 by American Association for the Advancement of Science


articles

Hallucinogenic amphetamine selectively destroys brain serotonin nerve terminals

G Ricaurte, G Bryan, L Strauss, L Seiden, and C Schuster

(+/-)-3,4-Methylenedioxyamphetamine (MDA), an amphetamine analog with hallucinogenic activity, produced selective long-lasting reductions in the level of serotonin, the number of serotonin uptake sites, and the concentration of 5-hydroxyindoleacetic acid in rat brain. Morphological studies suggested that these neurochemical deficits were due to serotonin nerve terminal degeneration. These results show that MDA has toxic activity for serotonin neurons in rats and raise the question of whether exposure to MDA and related hallucinogenic amphetamines can produce serotonin neurotoxicity in the human brain.


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Symptoms of anxiety and depression in childhood and use of MDMA: prospective, population based study.
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Effect of Glucoprivation on Serotonin Neurotoxicity Induced by Substituted Amphetamines.
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J. Pharmacol. Exp. Ther. 303, 831-839
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U. D. McCann, K. A. Lowe, and G. A. Ricaurte (1997)
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A Case of Toxic Psychosis Induced by 'Eve' (3,4-Methylenedioxyethylam-phetamine).
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Cloning of a serotonin transporter affected by antidepressants.
B. Hoffman, E Mezey, and M. Brownstein (1991)
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The Complications of 'Ecstasy' (MDMA).
K. Verebey, J. Alrazi, and J. H. Jaffe (1988)
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New data intensify the agony over ecstasy.
D. Barnes (1988)
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'Eve' and 'Ecstasy' A Report of Five Deaths Associated With the Use of MDEA and MDMA.
G. P. Dowling, E. T. McDonough III, and R. O. Bost (1987)
JAMA 257, 1615-1617
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