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Empagliflozin Enhances Autophagy, Mitochondrial Biogenesis, and Antioxidant Defense and Ameliorates Renal Ischemia/Reperfusion in Nondiabetic Rats

Moein Ala, Mohammad Reza Fallahpour Khoshdel, Ahmad Reza Dehpour

Oxidative Medicine and Cellular Longevity, 2022

71 citations

Abstract

Background . Recent meta‐analyses have shown that sodium‐glucose cotransporter 2 (SGLT‐2) inhibitors alleviate chronic kidney disease and acute kidney injury in diabetic patients. In this study, we aimed to investigate the effect of empagliflozin on renal ischemia/reperfusion (I/R) in nondiabetic rats and find the possible mechanisms. Experimental Approach . Eighteen male Wistar rats were randomly divided into three groups, including healthy control, ischemic control, and empagliflozin‐treated group. Thirty minutes of bilateral renal ischemia was induced by clamping the renal hilum. Forty‐eight hours after reopening the clamps, rats’ blood samples and tissue specimens were collected. Empagliflozin 10 mg/kg was administered by gavage, 2 hours before ischemia and 24 hours after the first dose. Results . I/R injury led to a significant rise in serum creatinine and blood urea nitrogen which was significantly decreased after treatment with empagliflozin. Empagliflozin also alleviated tubulointerstitial and glomerular damage and significantly decreased tissue histology scores. Empagliflozin decreased the increased levels of malondialdehyde, interleukin 1 β , and tumor necrosis factor α . SGLT2 inhibition increased the decreased expression of nuclear factor erythroid 2‐related factor 2 and PPARG coactivator 1 alpha that conduct antioxidant defense and mitochondrial biogenesis, respectively. Furthermore, empagliflozin markedly increased LC3‐II/LC3‐I and bcl2/bax ratios, showing its…

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