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• W1999041029 abstract "Hydrogen sulfide (H2S) is a novel endogenous gaseous signal transducer (gasotransmitter). Its emerging role in multiple facets of inter- and intra-cellular signaling as a metabolic, inflammatory, neuro and vascular modulator has been increasingly realized. Although H2S is known for its effects as an anti-hypertensive, anti-inflammatory and anti-oxidant molecule, the relevance of these effects in skeletal muscle biology during health and during metabolic syndromes is unclear. H2S has been implicated in vascular relaxation and vessel tone enhancement, which might lead to mitigation of vascular complications caused by the metabolic syndromes. Metabolic complications may also lead to mitochondrial remodeling by interfering with fusion and fission, therefore, leading to mitochondrial mitophagy and skeletal muscle myopathy. Mitochondrial protection by H2S enhancing treatments may mitigate deterioration of muscle function during metabolic syndromes. In addition, H2S might upregulate uncoupling proteins and might also cause browning of white fat, resulting in suppression of imbalanced cytokine signaling caused by abnormal fat accumulation. Likewise, as a source for H+ ions, it has the potential to augment anaerobic ATP synthesis. However, there is a need for studies to test these putative H2S benefits in different patho-physiological scenarios before its full-fledged usage as a therapeutic molecule. The present review highlights current knowledge with regard to exogenous and endogenous H2S roles in skeletal muscle biology, metabolism, exercise physiology and related metabolic disorders, such as diabetes and obesity, and also provides future directions." @default.
• W1999041029 created "2016-06-24" @default.
• W1999041029 creator A5003454740 @default.
• W1999041029 creator A5062805172 @default.
• W1999041029 date "2015-04-01" @default.
• W1999041029 modified "2023-10-16" @default.
• W1999041029 title "Role of hydrogen sulfide in skeletal muscle biology and metabolism" @default.
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• W1999041029 doi "https://doi.org/10.1016/j.niox.2014.11.012" @default.
• W1999041029 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4361234" @default.
• W1999041029 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25461301" @default.
• W1999041029 hasPublicationYear "2015" @default.
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