نتایج جستجو برای: mdma

تعداد نتایج: 1792  

Journal: :The Journal of pharmacology and experimental therapeutics 2010
K S Murnane W E Fantegrossi J R Godfrey M L Banks L L Howell

3,4-Methylenedioxymethamphetamine (MDMA) is an amphetamine derivative that elicits complex biological effects in humans. One plausible mechanism for this phenomenon is that racemic MDMA is composed of two stereoisomers that exhibit qualitatively different pharmacological effects. In support of this, studies have shown that R(-)-MDMA tends to have hallucinogen-like effects, whereas S(+)-MDMA ten...

Journal: :Genes, brain, and behavior 2012
N Fernàndez-Castillo M J Orejarena M Ribasés E Blanco M Casas P Robledo R Maldonado B Cormand

3,4-Methylenedioxymethamphetamine (MDMA, 'ecstasy') is a recreational drug widely used by adolescents and young adults. Although its rewarding effects are well established, there is controversy on its addictive potential. We aimed to compare the consequences of active and passive MDMA administration on gene expression in the mouse brain since all previous studies were based on passive MDMA admi...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Irene Antolino-Lobo Jan Meulenbelt Sandra M Nijmeijer Peter Scherpenisse Martin van den Berg Majorie B M van Duursen

Metabolism plays an important role in the toxic effects caused by 3,4-methylenedioxymethamphetamine (MDMA). Most research has focused on the involvement of CYP2D6 enzyme in MDMA bioactivation, and less is known about the contribution of other cytochrome P450 (P450) and phase II metabolism. In this study, we researched the differential roles of phase I P450 enzymes CYP1A2, CYP3A4, and CYP2D6 and...

1999
ANDREW C. McCREARY MICHAEL G. BANKSON KATHRYN A. CUNNINGHAM

The 5-hydroxytryptamine1B/1D (5-HT1B/1D) antagonist 29-methyl49-(5-methyl-[1,2,4]oxadiazol-3-yl)-biphenyl-4-carboxylic acid [4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-amide (GR 127935) and 5-HT1A antagonist N-(2-(4-(2-methoxyphenyl)-1piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide (WAY 100635) were used to assess whether hyperactivity induced by 3 mg/kg (1)-3,4-methylenedioxymetham...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2003
Mahmoud M Iravani Michael J Jackson Mikko Kuoppamäki Lance A Smith Peter Jenner

Ecstasy [3,4-methylenedioxymethamphetamine (MDMA)] was shown to prolong the action of L-3,4-dihydroxyphenylalanine (L-DOPA) while suppressing dyskinesia in a single patient with Parkinson's disease (PD). The clinical basis of this effect of MDMA is unknown but may relate to its actions on either dopaminergic or serotoninergic systems in brain. In normal, drug-naive common marmosets, MDMA admini...

Journal: :Brain research. Molecular brain research 2002
Weiping Peng Arumugam Premkumar Rainald Mossner Mitsunori Fukuda K Peter Lesch Rabi Simantov

3,4-Methylenedioxymethamphetamine (MDMA or Ecstasy) is a widely abused drug. In brains of mice exposed to MDMA, we recently detected altered expression of several cDNAs and genes by using the differential display polymerase chain reaction (PCR) method. Expression of one such cDNA, which exhibited 98% sequence homology with the synaptic vesicle protein synaptotagmin IV, decreased 2 h after MDMA ...

Journal: :Human brain mapping 2001
E Frei A Gamma R Pascual-Marqui D Lehmann D Hell F X Vollenweider

3,4-Methylenedioxymethamphetamine (MDMA; 'Ecstasy') is a psychostimulant drug producing heightened mood and facilitated social communication. In animal studies, MDMA effects are primarily mediated by serotonin (5-HT), but also by dopamine (DA) and possibly noradrenaline (NA). In humans, however, the neurochemical and neurophysiological basis of acute MDMA effects remains unknown. The distributi...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
João Paulo Capela Andreas Meisel Artur Reis Abreu Paula Sério Branco Luísa Maria Ferreira Ana Maria Lobo Fernando Remião Maria Lurdes Bastos Félix Carvalho

3,4-Methylenedioxymethamphetamine (MDMA or "Ecstasy") is a widely abused, psychoactive recreational drug. There is growing evidence that the MDMA neurotoxic profile may be highly dependent on both its hepatic metabolism and body temperature. Metabolism of MDMA involves N-demethylation to 3,4-methylenedioxyamphetamine (MDA), which is also a drug of abuse. MDMA and MDA are O-demethylenated to N-m...

Journal: :iranian red crescent medical journal 0
mitra behroozaghdam department of genetics, faculty of sciences, sciences and research branch, islamic azad university, tehran, ir iran mehrdad hashemi department of genetics, tehran medical sciences branch, islamic azad university, tehran, ir iran; department of genetics, tehran medical sciences branch, islamic azad university, tehran, ir iran. tel: +98-2122006664, fax: +21-22008049 gholamreza javadi department of genetics, faculty of sciences, sciences and research branch, islamic azad university, tehran, ir iran reza mahdian molecular medicine department, biotechnology research center, pasteur institute of iran, tehran, ir iran mansoureh soleimani cellular and molecular research center, iran university of medical sciences, tehran, ir iran; department of anatomy, iran university of medical sciences, tehran, ir iran

background 3-4methylenedioxymethamphetamine (mdma) is a synthetic and psychoactive drug, which is known popularly as ecstasy and has toxic effects on human organs. objectives considering the potential toxic interaction, this study was performed to quantify the expression of bax and bcl2 genes in mdma-induced hepatotoxicity on rat liver. subsequently, we evaluated pentoxifylline as a possible pr...

Objective(s): 3,4-Methylenedioxymethamphetamine (MDMA) is one of the most popular drugs of abuse in the world with hallucinogenic properties that has been shown to induce apoptosis in  liver cells. The present study aimed to investigate the effects of pentoxifylline (PTX) on liver damage induced by acute administration of MDMA in Wistar rat. Materials and Methods: Animals were administered wit...

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