The mixture of "ecstasy" and its metabolites is toxic to human SH-SY5Y differentiated cells at in vivo relevant concentrations

• Tipo: Artigo em Revista Científica Internacional
• Data: 2014

Autores

Daniel Jose Barbosa (Autor) Outra; Joao Paulo Capela (Autor) Outra; Renata Silva (Autor) Outra; Vania Vilas Boas (Autor) Outra; Luisa Maria Ferreira (Autor) Outra; Paula Serio Branco (Autor) Outra; Eduarda Fernandes (Autor) FFUP; Maria de Lourdes Bastos (Autor) FFUP; Felix Carvalho (Autor) FFUP

Revista

Título: Archives of Toxicology

Vol. 88

Páginas: 455-473

ISSN: 0340-5761

Editora: Springer Nature

Indexação

ISI Web of Knowledge - 24 Citações

Scopus - 35 Citações

Classificação Científica

FOS: Ciências médicas e da saúde > Medicina básica

Outras Informações

ID Authenticus: P-009-5GN

DOI: 10.1007/s00204-013-1120-7

Abstract (EN): The neurotoxicity of "ecstasy" (3,4-methylenedioxymethamphetamine, MDMA) is thought to involve hepatic metabolism, though its real contribution is not completely understood. Most in vitro neurotoxicity studies concern isolated exposures of MDMA or its metabolites, at high concentrations, not considering their mixture, as expected in vivo. Therefore, our postulate is that combined deleterious effects of MDMA and its metabolites, at low micromolar concentrations that may be attained into the brain, may elicit neurotoxicity. Using human SH-SY5Y differentiated cells as dopaminergic neuronal model, we studied the neurotoxicity of MDMA and its MDMA metabolites alpha-methyldopamine and N-methyl-alpha-methyldopamine and their correspondent glutathione and N-acetylcysteine monoconjugates, under isolated exposure and as a mixture, at normothermic or hyperthermic conditions. The results showed that the mixture of MDMA and its metabolites was toxic to SH-SY5Y differentiated cells, an effect potentiated by hyperthermia and prevented by N-acetylcysteine. As a mixture, MDMA and its metabolites presented a different toxicity profile, compared to each compound alone, even at equimolar concentrations. Caspase 3 activation, increased reactive oxygen species production, and intracellular Ca2+ raises were implicated in the toxic effect. The mixture increased intracellular glutathione levels by increasing its de novo synthesis. In conclusion, this study demonstrated, for the first time, that the mixture of MDMA and its metabolites, at low micromolar concentrations, which represents a more realistic approach of the in vivo scenario, elicited toxicity to human SH-SY5Y differentiated cells, thus constituting a new insight into the context of MDMA-related neurotoxicity.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 19