Polydatin protects against gouty nephropathy by inhibiting renal tubular cell pyroptosis. (3rd November 2022)

• Record Type: Journal Article
• Authors: Shi, Xingliang; Zhuang, Lili; Zhai, Zeqing; He, Yi; Sun, Erwei
• Is Part Of: International journal of rheumatic diseases. Volume 26:Number 1(2023)
• Page Start: 116
• Page End: 123
• Publication Date: 2022-11-03
• Subjects: gasdermin D -- gouty nephropathy -- NOD‐like receptor protein 3 -- polydatin -- pyroptosis; Rheumatology -- Periodicals; Rheumatology -- Asia -- Periodicals; Rheumatology -- Pacific Area -- Periodicals; Rheumatic Diseases -- Periodicals; Connective Tissue Diseases -- Periodicals; Immune System Diseases -- Periodicals; 616.723
• DOI: 10.1111/1756-185X.14463
• Languages: English
• ISSNs: 1756-1841

Abstract

Abstract: Objective: To investigate the protective effect and mechanism of polydatin (PD) against gouty nephropathy (GN) in mice. Methods: Twenty‐four mice were randomly divided into three groups: the control group (no treatment), the GN group (300 mg/kg hypoxanthine + 150 mg/kg potassium oxonate), and the GN + PD group (300 mg/kg hypoxanthine + 150 mg/kg potassium oxonate + 50 mg/kg PD). Histological changes in the kidneys and the levels of uric acid (UA), blood urea nitrogen (BUN), and serum creatinine (SCr) in the sera were measured. In addition, the expression of gasdermin D (GSDMD) protein in renal tubular epithelial cells, and the expression of NOD‐like receptor protein 3 (NLRP3), GSDMD, and caspase‐1 proteins in the kidney tissues were determined by immunohistochemistry, immunofluorescence, and Western blot. Results: In vitro, PD inhibited the expression of NLRP3, caspase‐1, and GSDMD and protected the renal tubular epithelial cells from pyroptosis. In vivo, PD treatment significantly ameliorated the pathological changes in kidney tissue, and reversed the decrease of serum UA and BUN in GN model mice. The expression of NLRP3, GSDMD, and caspase‐1 proteins was also decreased in the PD‐treated GN mice. Conclusion: The results suggest that PD has a protective effect on mice with GN, which may be related to the downregulation of NLRP3, GSDMD, and caspase‐1 proteins and the inhibition of renal tubular epithelial cells pyroptosis.