Tubular injury in diabetic kidney disease: molecular mechanisms and potential therapeutic perspectives

被引:41
作者
Wang, Yu [1 ,2 ]
Jin, Mingyue [1 ]
Cheng, Chak Kwong [3 ]
Li, Qiang [1 ]
机构
[1] Shenzhen Univ, Dept Endocrinol & Metab, Gen Hosp, Shenzhen, Guangdong, Peoples R China
[2] City Univ Hong Kong, Dept Biomed Sci, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Sch Biomed Sci, Hong Kong, Peoples R China
来源
FRONTIERS IN ENDOCRINOLOGY | 2023年 / 14卷
关键词
tubular injury; diabetic kidney disease; mechanism; therapy; programmed cell death; stem cell; ENDOPLASMIC-RETICULUM STRESS; MESENCHYMAL STEM-CELLS; OXIDATIVE STRESS; MINERALOCORTICOID RECEPTOR; PROXIMAL TUBULE; DIPEPTIDYL PEPTIDASE-4; SGLT2; INHIBITORS; EPITHELIAL-CELLS; ANGIOTENSIN-II; AUTOPHAGY;
D O I
10.3389/fendo.2023.1238927
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetic kidney disease (DKD) is a chronic complication of diabetes and the leading cause of end-stage renal disease (ESRD) worldwide. Currently, there are limited therapeutic drugs available for DKD. While previous research has primarily focused on glomerular injury, recent studies have increasingly emphasized the role of renal tubular injury in the pathogenesis of DKD. Various factors, including hyperglycemia, lipid accumulation, oxidative stress, hypoxia, RAAS, ER stress, inflammation, EMT and programmed cell death, have been shown to induce renal tubular injury and contribute to the progression of DKD. Additionally, traditional hypoglycemic drugs, anti-inflammation therapies, anti-senescence therapies, mineralocorticoid receptor antagonists, and stem cell therapies have demonstrated their potential to alleviate renal tubular injury in DKD. This review will provide insights into the latest research on the mechanisms and treatments of renal tubular injury in DKD.
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页数:19
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