Journal of Biological Chemistry · 2010 · 749 citations · 45 references
Life SciencesBiochemistryPhysiologyMetabolismMitochondrial BiologyRedox BiochemistryMetabolic Pathway DefectsMitochondrial Redox BiologyOxidative PhosphorylationReactive Oxygen SpeciesRedox MetabolismRedox SignalingCytochrome Electron TransferCytochrome Redox ChemistryHydrogen Sulfide ChemistryHydrogen Sulfide MetabolismOxidative Phosphorylation DeficiencyOxidative Phosphorylation DysfunctionOxidative Phosphorylation Redox ControlRedox Metabolism In Cardiovascular Disease
H(2)S, the most recently discovered gasotransmitter, might in fact be the evolutionary matriarch of this family, being both ancient and highly reduced. Disruption of gamma-cystathionase in mice leads to cardiovascular dysfunction and marked hypertension, suggesting a key role for this enzyme in H(2)S production in the vasculature. However, patients with inherited deficiency in gamma-cystathionase apparently do not present vascular pathology. A mitochondrial pathway disposes sulfide and couples it to oxidative phosphorylation while also exposing cytochrome c oxidase to this metabolic poison. This report focuses on the biochemistry of H(2)S biogenesis and clearance, on the molecular mechanisms of its action, and on its varied biological effects.
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