S-Nitrosoglutathione ameliorates acute renal dysfunction in a rat model of lipopolysaccharide-induced sepsis

Author:

Samuvel Devadoss J1,Shunmugavel Anandakumar2,Singh Avtar K1,Singh Inderjit2,Khan Mushfiquddin2

Affiliation:

1. Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA

2. Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA

Abstract

Abstract Objective Sepsis induces an inflammatory response that results in acute renal failure (ARF). The current study is to evaluate the role of S-Nitrosoglutathione (GSNO) in renoprotection from lipopolysaccharide (LPS)-induced sepsis. Methods Rats were divided to three groups. First group received LPS (5 mg/kg body weight), second group was treated with LPS + GSNO (50 μg/kg body weight), and third group was administered with vehicle (saline). They were sacrificed on day 1 and 3 post-LPS injection. Serum levels of nitric oxide (NO), creatinine and blood urea nitrogen (BUN) were analysed. Tissue morphology, T lymphocyte infiltrations, and the expression of inflammatory (TNF-α, iNOS) and anti-inflammatory (IL-10) mediators as well as glutathione (GSH) levels were determined. Key finding Lipopolysaccharide significantly decreased body weight and increased cellular T lymphocyte infiltration, caspase-3 and iNOS and decreased PPAR-γ in renal tissue. NO, creatinine and BUN were significantly elevated after LPS challenge, and they significantly decreased after GSNO treatment. TNF-α level was found significantly increased in LPS-treated serum and kidney. GSNO treatment of LPS-challenged rats decreased caspase-3, iNOS, TNF-α, T lymphocyte infiltration and remarkably increased levels of IL-10, PPAR-γ and GSH. Conclusion GSNO can be used as a renoprotective agent for the treatment of sepsis-induced acute kidney injury.

Funder

Heather Perkins Trew Foundation

NIH

National Center for Research Resources

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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