Altered Sulfide (H2S) Metabolism in Ethylmalonic Encephalopathy

被引:41
作者
Tiranti, Valeria [1 ]
Zeviani, Massimo [1 ]
机构
[1] Ist Ricovero & Cura Carattere Sci IRCCS Fdn, Pierfranco & Luisa Mariani Ctr Res Childrens Mito, Unit Mol Neurogenet, Inst Neurol Carlo Besta, Milan, Italy
关键词
CYSTATHIONINE-GAMMA-LYASE; HYDROGEN-SULFIDE; NITRIC-OXIDE; ENZYMATIC CAPACITY; N-ACETYLCYSTEINE; OXIDATION; ETHE1; MUTATIONS; SULFUR; TISSUE;
D O I
10.1101/cshperspect.a011437
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hydrogen sulfide (sulfide, H2S) is a colorless, water-soluble gas with a typical smell of rotten eggs. In the past, it has been investigated for its role as a potent toxic gas emanating from sewers and swamps or as a by-product of industrial processes. At high concentrations, H2S is a powerful inhibitor of cytochrome c oxidase; in trace amounts, it is an important signaling molecule, like nitric oxide (NO) and carbon monoxide (CO), together termed "gasotransmitters." This review will cover the physiological role and the pathogenic effects of H2S, focusing on ethylmalonic encephalopathy, a human mitochondrial disorder caused by genetic abnormalities of sulfide metabolism. We will also discuss the options that are now conceivable for preventing genetically driven chronic H2S toxicity, taking into account that a complete understanding of the physiopathology of H2S has still to be achieved.
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页数:11
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