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MDMA: all studies

Page 199 of 345: studies 1,981 to 1,990 of 3,446, newest first. Back to the MDMA overview

Research

MDMA produces a conditioned place preference and elicits ejaculation in male rats: a modulatory role for the endogenous opioids.

Pharmacology, Biochemistry, and Behavior October 1, 1991 E J Bilsky, C L Hubbell, J D Delconte et al.

Methylenedioxymethamphetamine (MDMA) can produce a conditioned place preference (CPP) among rats. The ability of MDMA to produce a CPP was assessed while some rats were under the influence of naltrexone, 56 mg/kg, given 4 h before conditioning. Naltrexone attenuated MDMA's ability to produce a CPP without completely blocking MDMA's effects. Having noticed previously the production of seminal...

DOI: 10.1016/0091-3057(91)90577-o (opens in new tab) Animals Rats, inbred strains N-methyl-3,4-methylenedioxyamphetamine Naltrexone +8

Lasting Neuropsychiatric Sequelae of (??)Methylenedioxymethamphetamine (???Ecstasy???) in Recreational Users

Journal of Clinical Psychopharmacology October 1, 1991 Una D. Mccann, George A. Ricaurte, Domenic A. Ciraulo 137 citations

Two persons are described who demonstrated prolonged neuropsychiatric syndromes after the ingestion of large doses of (+-)-3,4-methylenedioxymethamphetamine (MDMA), a recreationally used amphetamine analog. These cases suggest that MDMA, known to be neurotoxic to serotonin neurons in several experimental animals, may also produce untoward effects in humans. In addition, they provide evidence...

Neuroanatomic specificity and time course of alterations in rat brain serotonergic pathways induced by MDMA (3,4‐methylenedioxymethamphetamine): Assessment using quantitative autoradiography

Synapse August 1, 1991 George Battaglia, John Sharkey, Michael J. Kuhar et al. 113 citations

Abstract The Widely abused “designer” durg MDMA (3,4‐methylenedioxymethamphetamine) has been shown to caused marked and long‐lasting changes in brain serotonergic systems. The present study uses quantitative in vitro autoradiography of 3 H‐paroxetine labeled 5‐HT uptake sites to assess the time‐dependent effects of MDMA on 5‐HT neurons in specific neuroanatomic loci. Following treatment with...

The neurochemical and stimulatory effects of putative metabolites of 3,4-methylenedioxyamphetamine and 3,4-methylenedioxymethamphetamine in rats.

Pharmacology, Biochemistry, and Behavior July 1991 S Y Yeh, F L Hsu

Rats were injected SC with a dose of 10 mg/kg (as base) of 3,4-methylenedioxyamphetamine (MDA), or 3,4-methylenedioxymethamphetamine (MDMA), 4-hydroxy-3-methoxyamphetamine, alpha-methyldopamine and alpha-methylnorepinephrine, metabolites of MDA, and alpha-methylepinephrine, a putative metabolite of MDMA, twice daily for either 5 or 7 consecutive doses. The rats were killed 24 h after the last...

The effects of repeated administration of MDMA on the expression of sexual behavior in the male rat.

Pharmacology, Biochemistry, and Behavior July 1, 1991 W A Dornan, J L Katz, George A. Ricaurte

3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy") is a potent neurotoxin which preferentially produces 5-HT nerve terminal degeneration in the CNS in both rodents and primates. Timely research on the behavioral effects of acute and long term treatment of MDMA is critical due to the neuropathological effects of MDMA and its abuse liability. Presently, there are no published reports that have...

DOI: 10.1016/0091-3057(91)90171-w (opens in new tab) Serotonin Hippocampus Corpus striatum Animals +8

New Age Seekers: MDMA Use as an Adjunct to Spiritual Pursuit

Journal of Psychoactive Drugs July 1, 1991 Lynne Watson, Jerome Beck 32 citations

The use of MDMA as an adjunct to spiritual pursuit among New Ager seekers is examined. These study respondents indicated that social worlds greatly influenced which qualities of the MDMA experience were most pursued and valued. In contrast to recreationally oriented respondents, who saw minimal long-term benefits accruing from MDMA use, New Agers typically believed that carefully planned...

Synthesis and pharmacological examination of 1-(3-methoxy-4-methylphenyl)-2-aminopropane and 5-methoxy-6-methyl-2-aminoindan: similarities to 3,4-(methylenedioxy)methamphetamine (MDMA)

Journal of Medicinal Chemistry May 1, 1991 Michael P. Johnson, Stewart Frescas, Robert Oberlender et al. 53 citations

The racemate and the enantiomers of 1-(3-methoxy-4-methyphenyl)-2- aminopropane (6) and racemic 5-methoxy-6-methyl-2-aminoindan (11) were tested for stimulus generalization in the two-lever drug-discrimination paradigm. Both 6 and 11 were found to substitute with high potency in 3,4-(methylenedioxy)methamphetamine (1) and (S)-1-(1,3-benzodioxol-5-yl)-2-(methylamino)butane (2) trained rats. In...

DOI: 10.1021/jm00109a020 (opens in new tab) MDMA Methylenedioxy Methamphetamine Stereochemistry +2

Chronic paranoid psychosis after misuse of MDMA ("ecstasy")

BMJ March 23, 1991 Philip Mcguire, Thomas Fahy 128 citations

Methylenedioxymetamphetamine (MDMA, "ecstasy") is a hallucinogenic amphetamine that combines the effects of amphetamines and lysergic acid diethylamide (LSD) and has become increasingly popular in the United Kingdom.We report two cases of chronic paranoid psychoses after heavy misuse of this drug. Case reports CASE I

Assessment of the role of alpha-methylepinine in the neurotoxicity of MDMA.

Pharmacology, Biochemistry, and Behavior February 1991 T D Steele, W K Brewster, M P Johnson et al.

To assess the potential involvement of metabolism of 3,4-methylenedioxymethamphetamine (MDMA) to the catechol alpha-methylepinine in producing serotonergic neurotoxicity, we attempted to correlate aspects of this reaction with the neurotoxicity profile of MDMA. In contrast to the stereoselectivity of S-(+)-MDMA in causing persistent declines in rat brain 5-hydroxyindole levels, no...

Selective 5-hydroxytryptamine2 receptor antagonists protect against the neurotoxicity of methylenedioxymethamphetamine in rats.

Journal of Pharmacology and Experimental Therapeutics November 1, 1990 Christopher J. Schmidt, Gina M. Abbate, Christine K. Black et al.

The serotonergic deficits resulting from methylenedioxymethamphetamine (MDMA)-induced neurotoxicity were prevented by the simultaneous administration of 5-hydroxytryptamine2 (5-HT2) receptor antagonists such as MDL 11,939 or ritanserin. This effect was not region specific as protection was observed in the cortex, hippocampus and striatum 1 week after the administration of a single dose of MDMA....