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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