The FASEB Journal · 2004 · 874 citations · 33 references
Life SciencesNeurobiologyNeuroscienceMolecular NeuroscienceNeurochemistryRedox BiochemistryAntioxidant DefenseGlutathione MetabolismNeuronal MetabolismNeuroprotectionOxidative StressReactive Oxygen SpeciesGlutamate-induced NeurotoxicityGlutathione HomeostasisGlutathione ProtectionGlutathione S-transferasesGlutathione SystemNeural Cell DeathOxidative Stress DefenseOxidative Stress Injury
Hydrogen sulfide (H2S), which is a well-known toxic gas, is found in relatively high concentrations in the brain. Although a neuromodulatory role of H2S has been demonstrated, little is known of its other biological functions. Here we show that H2S protects primary cultures of neurons from death in a well-studied model of oxidative stress caused by glutamate, a process called oxidative glutamate toxicity--or oxytosis. We found that H2S increases the glutathione levels, which normally decrease during the cell death cascade, by enhancing the activity of gamma-glutamylcysteine synthetase and up-regulating cystine transport. Cystine (cysteine) is the rate-limiting substrate of glutathione synthesis. These observations reveal that H2S protects neurons from oxytosis by increasing the production of the antioxidant glutathione.
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Glutamate neurotoxicity and diseases of the nervous system
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The vasorelaxant effect of H2S as a novel endogenous gaseous KATP channel opener
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