Journal
NEUROREPORT
Volume 23, Issue 4, Pages 216-219Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WNR.0b013e32834fe6d6
Keywords
beta-N-methylamino-L-alanine; glutathione; methylmercury; oxidative stress
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Determination of the environmental factors involved in neurodegenerative diseases has been elusive. Methylmercury and beta-N-methylamino-L-alanine (BMAA) have both been implicated in this role. Exposure of primary cortical cultures to these compounds independently induced concentration-dependent neurotoxicity. Importantly, concentrations of BMAA (10-100 mu M) that caused no toxicity alone potentiated methylmercury (3 mu M) toxicity. In addition, concentrations of BMAA and methylmercury that had no effect by themselves on the main cellular antioxidant glutathione together decreased glutathione levels. Furthermore, the combined toxicity of methylmercury and BMAA was attenuated by the cell permeant form of glutathione, glutathione monoethyl ester. The results indicate a synergistic toxic effect of the environmental neurotoxins BMAA and methylmercury, and that the interaction is at the level of glutathione depletion. NeuroReport 23:216-219 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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