Sodium-glucose cotransporter inhibitors and oxidative stress: An update

被引:119
|
作者
Yaribeygi, Habib [1 ,2 ]
Atkin, Stephen L. [3 ]
Butler, Alexandra E. [4 ]
Sahebkar, Amirhossein [5 ,6 ,7 ]
机构
[1] Baqiyatallah Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Chron Kidney Dis Res Ctr, Tehran, Iran
[3] Weill Cornell Med Qatar, Doha, Qatar
[4] Antidoping Lab Qatar, Life Sci Res Div, Doha, Qatar
[5] Mashhad Univ Med Sci, Neurogen Inflammat Res Ctr, Mashhad, Iran
[6] Mashhad Univ Med Sci, Pharmaceut Technol Inst, Biotechnol Res Ctr, Mashhad, Iran
[7] Mashhad Univ Med Sci, Sch Pharm, Mashhad, Iran
关键词
diabetes; free radicals; glycosuria; oxidative stress; SGLT2; inhibitors; GLYCATION END-PRODUCTS; SGLT2; INHIBITORS; VITAMIN-C; MITOCHONDRIAL DYSFUNCTION; EMPAGLIFLOZIN IMPROVES; CARDIOVASCULAR-DISEASE; SELECTIVE INHIBITOR; TUBULAR CELL; INFLAMMATION; ANTIOXIDANT;
D O I
10.1002/jcp.26760
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are therapeutic agents that have been used recently to reduce tubular absorption of glucose, leading to enhanced glycosuria, resulting in the reduction of blood glucose and improved diabetes control. Recent data suggest that SGLT2 inhibitors have antioxidant properties that may be key to the reduction in cardiovascular death found in clinical trials. Oxidative stress is involved in the development and progression of atherosclerosis, as well as underlying diabetes complications, and may result from either increased free-radical production, a reduction in antioxidative capacity, or a combination of both. In this report, we have reviewed the recent evidence of the impact that SGLT2 inhibition may have on improved oxidative stress by either amelioration of free-radical generation or potentiation of cellular antioxidative capacity, and its importance in the prevention of cardiovascular and diabetes complications.
引用
收藏
页码:3231 / 3237
页数:7
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