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MDMA: all studies

Page 96 of 346: studies 951 to 960 of 3,454, newest first. Back to the MDMA overview

Research

Catechol-o-methyltransferase and 3,4-({+/-})-methylenedioxymethamphetamine toxicity.

Toxicological sciences : an official journal of the Society of Toxicology May 2014 Joseph M Herndon, Aram B Cholanians, Lucina E Lizarraga et al.

Metabolism of 3,4-(±)-methylenedioxymethamphetamine (MDMA) is necessary to elicit its neurotoxic effects. Perturbations in phase I and phase II hepatic enzymes can alter the neurotoxic profile of systemically administered MDMA. In particular, catechol-O-methyltransferase (COMT) plays a critical role in determining the fraction of MDMA that is converted to potentially neurotoxic metabolites....

DOI: 10.1093/toxsci/kfu035 (opens in new tab) Full text (opens in new tab) 3,4-±-methylenedioxymethamphetamine Catechol-o-methyltransferase Hyperthermia

Plasma oxytocin concentrations following MDMA or intranasal oxytocin in humans

Psychoneuroendocrinology April 19, 2014 M. Kirkpatrick, Sunday M. Francis, Royce Lee et al. 106 citations

MDMA (±3,4-methylenedioxymethamphetamine, ‘ecstasy’) is reportedly used recreationally because it increases feelings of sociability and interpersonal closeness. Prior work suggests that the pro-social effects of MDMA may be mediated by release of oxytocin. A direct examination of plasma levels of oxytocin after acute doses of oxytocin and MDMA, in the same individuals, would provide further...

Elucidating the neurotoxic effects of MDMA and its analogs.

Life Sciences April 17, 2014 Senthilkumar S Karuppagounder, Dwipayan Bhattacharya, Manuj Ahuja et al.

There is a rapid increase in the use of methylenedioxymethamphetamine (MDMA) and its structural congeners/analogs globally. MDMA and MDMA-analogs have been synthesized illegally in furtive dwellings and are abused due to its addictive potential. Furthermore, MDMA and MDMA-analogs have shown to have induced several adverse effects. Hence, understanding the mechanisms mediating this neurotoxic...

DOI: 10.1016/j.lfs.2014.02.010 (opens in new tab) Full text (opens in new tab) Drugs of abuse MDMA & Analogs Mitochondrial dysfunction Neurotoxicity +1

MDMA alters emotional processing and facilitates positive social interaction

Psychopharmacology April 12, 2014 Margaret C. Wardle, Harriet de Wit 97 citations

±3,4-Methylenedioxymethamphetamine (MDMA, “ecstasy”) produces “prosocial” effects, such as feelings of empathy and closeness, thought to be important to its abuse and its value in psychotherapy. However, it is not fully understood how MDMA alters basic emotional processes to produce these effects, or whether it produces corresponding changes in actual social behavior. Here, we examined how MDMA...

‘Ecstasy’ as a social drug: MDMA preferentially affects responses to emotional stimuli with social content

Social Cognitive and Affective Neuroscience March 27, 2014 Margaret C. Wardle, Matthew G. Kirkpatrick, Harriet de Wit 52 citations

3,4-Methylenedioxymethamphetamine (MDMA, 'ecstasy') is used recreationally to improve mood and sociability, and has generated clinical interest as a possible adjunct to psychotherapy. One way that MDMA may produce positive 'prosocial' effects is by changing responses to emotional stimuli, especially stimuli with social content. Here, we examined for the first time how MDMA affects subjective...

Altered energy production, lowered antioxidant potential, and inflammatory processes mediate CNS damage associated with abuse of the psychostimulants MDMA and methamphetamine.

European Journal of Pharmacology March 15, 2014 Luke A. Downey, Jennifer M Loftis

Central nervous system (CNS) damage associated with psychostimulant dependence may be an ongoing, degenerative process with adverse effects on neuropsychiatric function. However, the molecular mechanisms regarding how altered energy regulation affects immune response in the context of substance use disorders are not fully understood. This review summarizes the current evidence regarding the...

DOI: 10.1016/j.ejphar.2014.01.032 (opens in new tab) Full text (opens in new tab) 2-fluoro-2-deoxy-d-glucose pubchem cid 3,4-Methylenedioxy-N-Methylamphetamine MDMA Bioenergetics Cocaine pubchem cid +4

MDMA effects consistent across laboratories

Psychopharmacology March 15, 2014 M. Kirkpatrick, Matthew J. Baggott, John Mendelson et al. 78 citations

Several laboratories have conducted placebo-controlled drug challenge studies with 3,4-methylenedioxymethamphetamine (MDMA), providing a unique source of data to examine the reliability of the acute effects of the drug across subject samples and settings. We examined the subjective and physiological responses to the drug across three different laboratories and investigated the influence of...

Methamphetamine and MDMA: ‘Safe’ drugs of abuse

March 1, 2014 Allana M. Krolikowski, A. Koyfman

Methamphetamine and MDMA have been called safe drugs of abuse. Worldwide there is an increased consumption of these drugs, which has become a focus of research in South Africa. As the number of methamphetamine users has increased in many African countries, it is essential that emergency care practitioners are able to diagnose and manage intoxication with methamphetamine, MDMA, and other...

Glial cell response to 3,4-(+/-)-methylenedioxymethamphetamine and its metabolites.

Toxicological sciences : an official journal of the Society of Toxicology March 2014 Joseph M Herndon, Aram B Cholanians, Serrine S. Lau et al.

3,4-(±)-Methylenedioxymethamphetamine (MDMA) and 3,4-(±)-methylenedioxyamphetamine (MDA), a primary metabolite of MDMA, are phenylethylamine derivatives that cause serotonergic neurotoxicity. Although several phenylethylamine derivatives activate microglia, little is known about the effects of MDMA on glial cells, and evidence of MDMA-induced microglial activation remains ambiguous. We...

DOI: 10.1093/toxsci/kft275 (opens in new tab) Full text (opens in new tab) 3,4-±-methylenedioxymethamphetamine Metabolites Microglial activation.

MDMA is certainly damaging after 25 years of empirical research: a reply and refutation of Doblin et al. (2014).

Human Psychopharmacology: Clinical and Experimental March 2014 Andrew C. Parrott

Human Psychopharmacology recently published my review into the increase in empirical knowledge about the human psychobiology of MDMA over the past 25 years (Parrott, 2013a). Deficits have been demonstrated in retrospective memory, prospective memory, higher cognition, complex visual processing, sleep architecture, sleep apnoea, pain, neurohormonal activity, and psychiatric status. Neuroimaging...