Dapagliflozin alleviates renal inflammation and protects against diabetic kidney diseases, both dependent and independent of blood glucose levels

• Published in: Frontiers in immunology Vol. 14; p. 1205834
• Main Authors: Cai, Anxiang, Shen, Jianxiao, Yang, Xiaoqian, Shao, Xinghua, Gu, Leyi, Mou, Shan, Che, Xiajing
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 2023
• Subjects: Animals; Blood Glucose - metabolism; Diabetes Mellitus, Experimental - complications; Diabetes Mellitus, Experimental - drug therapy; diabetic kidney disease; Diabetic Nephropathies - drug therapy; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - prevention & control; inflammation; Inflammation - pathology; macrophage; Mice; Nephritis - complications; renal tubular cell; sodium-glucose cotransporter 2 inhibitors; Sodium-Glucose Transporter 2 Inhibitors - pharmacology; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use; diabetic kidney disease; sodium-glucose cotransporter 2 inhibitors; renal tubular cell; macrophage; inflammation
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2023.1205834

Diabetic kidney disease (DKD) has become the leading cause of end-stage renal disease worldwide. Therefore, efforts to understand DKD pathophysiology and prevent its development at the early phase are highly warranted. Here, we analyzed kidneys from healthy mice, diabetic mice, and diabetic mice treated with the sodium-glucose cotransporter 2 inhibitor dapagliflozin using ATAC and RNA sequencing. The findings were verified at the protein levels and in cultured cells. Our combined method of ATAC and RNA sequencing revealed , , and as the key candidate genes associated with hyperglycemia, azotemia, and albuminuria. Their protein levels were altered together with multiple other inflammatory cytokines in the diabetic kidney, which was alleviated by dapagliflozin treatment. Cell culture of immortalized renal tubular cells and macrophages unraveled that dapagliflozin could directly effect on these cells as an anti-inflammatory agent independent of glucose concentrations. We further proved that dapagliflozin attenuated ischemia/reperfusion-induced chronic kidney injury and renal inflammation in mice. Overall, our data emphasize the importance of inflammatory factors to the pathogenesis of DKD, and provide valuable mechanistic insights into the renoprotective role of dapagliflozin.