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Maria L Bastos

5 papers in the library · publishing 2006-2018

Papers

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Aged rats are more vulnerable than adolescents to "ecstasy"-induced toxicity.

Archives of Toxicology July 2018 R Feio-Azevedo, V M Costa, D J Barbosa et al.

3,4-Methylenedioxymethamphetamine (MDMA or "ecstasy") is a widespread drug of abuse with known neurotoxic properties. The present study aimed to evaluate the differential toxic effects of MDMA in adolescent and aged Wistar rats, using doses pharmacologically comparable to humans. Adolescent (post-natal day 40) (3 × 5 mg/kg, 2 h apart) and aged (mean 20 months old) (2 × 5 mg/kg, 2 h apart) rats...

DOI: 10.1007/s00204-018-2226-8 (opens in new tab) Full text (opens in new tab) Aged rats Cardiotoxicity Nephrotoxicity Neurotoxicity +2

Modeling chronic brain exposure to amphetamines using primary rat neuronal cortical cultures.

Neuroscience September 26, 2014 T B Nogueira, Silvana Da Costa Araújo, F Carvalho et al.

Amphetamine-type psychostimulants (ATS) are used worldwide by millions of patients for several psychiatric disorders. Amphetamine (AMPH) and "ecstasy" (3,4-methylenedioxymethamphetamine or MDMA) are common drugs of abuse. The impact of chronic ATS exposure to neurons and brain aging is still undisclosed. Current neuronal culture paradigms are designed to access acute ATS toxicity. We report for...

DOI: 10.1016/j.neuroscience.2014.07.009 (opens in new tab) Full text (opens in new tab) Amphetamines Chronic exposure Cortical neurons Long-term neuronal cultures +2

Mechanisms underlying the hepatotoxic effects of ecstasy.

Current Pharmaceutical Biotechnology August 1, 2010 Márcia Carvalho, Helena Pontes, Fernando Remião et al.

3,4-Methylenedioxymethamphetamine (MDMA or ecstasy) is a worldwide illegally used amphetamine-derived designer drug known to be hepatotoxic to humans. Jaundice, hepatomegaly, centrilobular necrosis, hepatitis and fibrosis represent some of the adverse effects caused by MDMA in the liver. Although there is irrefutable evidence of MDMA-induced hepatocellular damage, the mechanisms responsible for...

DOI: 10.2174/138920110791591535 (opens in new tab) Full text (opens in new tab) Liver Animals Humans N-methyl-3,4-methylenedioxyamphetamine +2

Neurotoxicity mechanisms of thioether ecstasy metabolites.

Neuroscience June 8, 2007 J P Capela, Carla Macedo, P S Branco et al.

3,4-Methylenedioxymethamphetamine (MDMA or "ecstasy"), is a widely abused, psychoactive recreational drug that is known to induce neurotoxic effects. Human and rat hepatic 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-methyl-alpha-methyldopamine (N-Me-alpha-MeDA) and alpha-methyldopamine...

Ecstasy-induced cell death in cortical neuronal cultures is serotonin 2A-receptor-dependent and potentiated under hyperthermia.

Neuroscience 2006 J P Capela, Karsten Ruscher, M Lautenschlager et al.

Studies on 3,4-methylenedioxymethamphetamine ("ecstasy")-induced neurotoxicity mainly focus on damage of serotonergic terminals. Less attention has been given to neuronal cell death produced by 3,4-methylenedioxymethamphetamine and other amphetamines in areas including the cortex, striatum and thalamus. In the present study we investigated 3,4-methylenedioxymethamphetamine-induced neurotoxicity...