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Hydrogen Sulfide: Recent Progression and Perspectives for the Treatment of Diabetic Nephropathy

Hai-Jian Sun, Zhi-Yuan Wu, Lei Cao and 6 more

Molecules · 2019

doi:10.3390/molecules24152857 (opens in a new tab)

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Abstract

Diabetic kidney disease develops in approximately 40% of diabetic patients and is a major cause of chronic kidney diseases (CKD) and end stage kidney disease (ESKD) worldwide. Hydrogen sulfide (H<sub>2</sub>S), the third gasotransmitter after nitric oxide (NO) and carbon monoxide (CO), is synthesized in nearly all organs, including the kidney. Though studies on H<sub>2</sub>S regulation of renal physiology and pathophysiology are still in its infancy, emerging evidence shows that H<sub>2</sub>S production by renal cells is reduced under disease states and H<sub>2</sub>S donors ameliorate kidney injury. Specifically, aberrant H<sub>2</sub>S level is implicated in various renal pathological conditions including diabetic nephropathy. This review presents the roles of H<sub>2</sub>S in diabetic renal disease and the underlying mechanisms for the protective effects of H<sub>2</sub>S against diabetic renal damage. H<sub>2</sub>S may serve as fundamental strategies to treat diabetic kidney disease. These H<sub>2</sub>S treatment modalities include precursors for H<sub>2</sub>S synthesis, H<sub>2</sub>S donors, and natural plant-derived compounds. Despite accumulating evidence from experimental studies suggests the potential role of the H<sub>2</sub>S signaling pathway in the treatment of diabetic nephropathy, these results need further clinical translation. Expanding understanding of H<sub>2</sub>S in the kidney may be vital to translate H<sub>2</sub>S to be a novel therapy for diabetic renal disease.

Abstract licence: CC BY

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