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Aram B Cholanians

4 papers in the library · publishing 2014-2019

Papers

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Concurrent Inhibition of Vesicular Monoamine Transporter 2 Does Not Protect Against 3,4-Methylenedioxymethamphetamine (Ecstasy) Induced Neurotoxicity.

Toxicological sciences : an official journal of the Society of Toxicology July 1, 2019 Aram B Cholanians, Andy V Phan, Serrine S. Lau et al.

3, 4-Methylenedioxymethamphetamine (MDMA) is a hallucinogenic amphetamine derivative. The acute effects of MDMA are hyperthermia, hyperactivity, and behavioral changes, followed by long-term serotonergic neurotoxicity in rats and primates. However, the underlying mechanisms of MDMA neurotoxicity remain elusive. We reported that pretreatment of rats with Ro 4-1284, a reversible inhibitor of the...

Vesicular monoamine transporter 2 and the acute and long-term response to 3,4-(±)-methylenedioxymethamphetamine.

Toxicological sciences : an official journal of the Society of Toxicology January 2015 Lucina E Lizarraga, Aram B Cholanians, Andy V Phan et al.

3,4-(±)-Methylenedioxymethamphetamine (MDMA, Ecstasy) is a ring-substituted amphetamine derivative with potent psychostimulant properties. The neuropharmacological effects of MDMA are biphasic in nature, initially causing synaptic monoamine release, primarily of serotonin (5-HT). Conversely, the long-term effects of MDMA manifest as prolonged depletions in 5-HT, and reductions in 5-HT reuptake...

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

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.