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MDMA: all studies

Page 132 of 346: studies 1,311 to 1,320 of 3,454, newest first. Back to the MDMA overview

Research

Methylenedioxymethamphetamine (MDMA)-related fatalities in Australia: demographics, circumstances, toxicology and major organ pathology.

Drug and Alcohol Dependence October 1, 2009 Sharlene Kaye, Shane Darke, Johan Duflou

To examine the demographic characteristics, circumstances, toxicology and major organ pathology of MDMA-related deaths in Australia. Retrospective review of cases in which MDMA was a cause of death, as identified from the National Coronial Information System. 82 cases over a 5-year period were identified. The majority of decedents were male (83%), with a median age of 26 years. Deaths were...

Further studies on the role of metabolites in (+/-)-3,4-methylenedioxymethamphetamine-induced serotonergic neurotoxicity.

Drug Metabolism and Disposition October 2009 Melanie Mueller, Jie Yuan, Anne Felim et al.

The mechanism by which the recreational drug (+/-)-3,4-methylenedioxymethamphetamine (MDMA) destroys brain serotonin (5-HT) axon terminals is not understood. Recent studies have implicated MDMA metabolites, but their precise role remains unclear. To further evaluate the relative importance of metabolites versus the parent compound in neurotoxicity, we explored the relationship between...

MDMA pretreatment leads to mild chronic unpredictable stress-induced impairments in spatial learning.

Behavioral Neuroscience October 1, 2009 Jacobi I. Cunningham, Jamie Raudensky, John Tonkiss et al. 27 citations

3,4-Methylenedioxymethamphetamine (MDMA) is a drug of abuse worldwide and a selective serotonin (5-HT) neurotoxin. An important factor in the risk of drug abuse and relapse is stress. Although multiple parallels exist between MDMA abuse and stress, including effects on 5-HTergic neurotransmission, few studies have investigated the consequences of combined exposure to MDMA and chronic stress....

DOI: 10.1037/a0016716 (opens in new tab) MDMA Serotonergic Serotonin transporter Hippocampus +3

Enzymatic–nonenzymatic cellular antioxidant defense systems response and immunohistochemical detection of MDMA, VMAT2, HSP70, and apoptosis as biomarkers for MDMA (Ecstasy) neurotoxicity

Journal of Neuroscience Research October 1, 2009 Irene Riezzo, Daniela Cerretani, Carmela Fiore et al. 47 citations

Abstract 3,4‐Methylenedioxymethamphetamine (MDMA)‐induced neurotoxicity leads to the formation of quinone metabolities and hydroxyl radicals and then to the production of reactive oxygen species (ROS). We evaluated the effect of a single dose of MDMA (20 mg/kg, i.p.) on the enzymatic and nonenzymatic cellular antioxidant defense system in different areas of rat brain in the early hours (<6 hr)...

Neurocognitive impairments in MDMA and other drug users: MDMA alone may not be a cognitive risk factor

Journal of Clinical and Experimental Neuropsychology September 30, 2009 Karen L. Hanson, Mónica Luciana 34 citations

This study and our previous report (Hanson, Luciana, & Sullwold, 2008) suggest that moderate MDMA use does not lead to persistent impairments above and beyond that associated with generally heavy drug use, but polydrug use may lead to dose-related temporal and frontoparietal dysfunction. Marijuana use may be particularly problematic. Cause-effect relations are unclear.

Neurotoxicity of drugs of abuse - the case of methylenedioxy amphetamines (MDMA, ecstasy ), and amphetamines

Dialogues in Clinical Neuroscience September 30, 2009 Euphrosyne Gouzoulis‐mayfrank, Jörg Daumann 115 citations

Ecstasy (MDMA, 3,4-methylendioxymethamphetamine) and the stimulants methamphetamine (METH, speed) and amphetamine are popular drugs among young people, particularly in the dance scene. When given in high doses both MDMA and the stimulant amphetamines are clearly neurotoxic in laboratory animals. MDMA causes selective and persistent lesions of central serotonergic nerve terminals, whereas...

MDMA-induced serotonergic neurotoxicity enhances aggressiveness in low- but not high-aggressive rats.

European Journal of Pharmacology September 15, 2009 Alinde E Wallinga, Anna M Ten Voorde, Sietse F De Boer et al.

Ecstasy or 3,4-methylenedioxymethamphetamine (MDMA) is a frequently (ab)used recreational drug for its acute euphoric effects but on the long-term may cause neurotoxic damage to serotonin (5-hydroxytryptamine; 5-HT) nerve endings in the brain. Since decreased brain 5-HT function has been strongly associated with several impulse control disorders like hostility and violent aggression, ecstasy...

PRECLINICAL STUDY: Acquisition and reinstatement of MDMA‐induced conditioned place preference in mice pre‐treated with MDMA or cocaine during adolescence

Addiction Biology September 8, 2009 Manuel Daza‐losada, Marta Rodríguez‐arias, María A. Aguilar et al. 37 citations

ABSTRACT Those who take ecstasy are more likely to consume other drugs than non‐users with cocaine abuse being reported by 75.5% of high school student MDMA (± 3,4‐methylenedioxymetamphetamine hydrochloride) users. The aim of this work was to evaluate the effects of exposure during adolescence to MDMA, cocaine or to both drugs on the MDMA‐induced conditioned place preference (CPP) in adult...

Neuroendocrine and subjective responses to pharmacological challenge with citalopram: a controlled study in male and female ecstasy/MDMA users.

Journal of Psychopharmacology September 2009 K Allott, B K Canny, J H Broadbear et al.

Despite evidence that +/-3,4-methylenedioxymethamphetamine (MDMA; 'ecstasy') causes persistent alterations to the serotonergic system of animals, evidence for long-term neurological effects of ecstasy/MDMA in humans remains equivocal. The current study assessed serotonin functioning of nine male and 11 female recreational ecstasy polydrug users by measuring neuroendocrine (prolactin, cortisol)...