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doi:10.1073/pnas.1300873110

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S-glutathionylation reactions in mitochondria Non-enzymatic protein S-glutathionylation Protein cysteine SH groups can be subjected to a range of different redox modifications which are dependent on H 2 O 2 levels, GSSG concentration, presence of H 2 S, availability of nitric oxide, proximity of neighboring SH groups (for inter or intramolecular disulfide formation), proximity of amides or sulfenic acid residues (Goubern et al., 2013b)

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Conclusion: Hyperammonemia induced mitochondrial oxidative and intermediary metabolite abnormalities with impaired protein synthesis are mediated via HIF1, a novel target for potential therapeutics to treat sarcopenia in cirrhosis

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