Sodium-Glucose Cotransporter-2 Inhibitors in Vascular Biology: Cellular and Molecular Mechanisms

被引:6
|
作者
Xiao, Lei [1 ]
Nie, Xin [2 ]
Cheng, Yanyan [2 ]
Wang, Nanping [3 ,4 ]
机构
[1] Xi An Jiao Tong Univ, Cardiovasc Res Ctr, Sch Basic Med Sci, Xian 710061, Peoples R China
[2] Dalian Med Univ, Adv Inst Med Sci, Dalian 116044, Peoples R China
[3] Peking Univ, Hlth Sci Ctr, Key Lab Mol Cardiovasc Sci, Minist Educ, Beijing 100191, Peoples R China
[4] Peking Univ, Hlth Sci Ctr, Inst Cardiovasc Sci, Beijing 100191, Peoples R China
基金
美国国家科学基金会;
关键词
Sodium-glucose cotransporter-2 inhibitor; Vascular biology; Type 2 diabetes mellitus; Pharmacology; Mechanisms; INTIMA-MEDIA THICKNESS; PULSE-WAVE VELOCITY; SERUM URIC-ACID; INADEQUATE GLYCEMIC CONTROL; TYPE-2; DIABETIC-PATIENTS; SGLT2; INHIBITORS; BLOOD-PRESSURE; CARDIOVASCULAR EVENTS; OXIDATIVE STRESS; ATHEROSCLEROSIS PROGRESSION;
D O I
10.1007/s10557-021-07216-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sodium-glucose cotransporter-2 (SGLT2) inhibitors are new antidiabetic drugs that reduce hyperglycemia by inhibiting the glucose reabsorption in renal proximal tubules. Clinical studies have shown that SGLT2 inhibitors not only improve glycemic control but also reduce major adverse cardiovascular events (MACE, cardiovascular and total mortality, fatal or nonfatal myocardial infarction or stroke) and hospitalization for heart failure (HF), and improve outcome in chronic kidney disease. These cardiovascular and renal benefits have now been confirmed in both diabetes and non-diabetes patients. The precise mechanism(s) responsible for the protective effects are under intensive investigation. This review examines current evidence on the cardiovascular benefits of SGLT2 inhibitors, with a special emphasis on the vascular actions and their potential mechanisms.
引用
收藏
页码:1253 / 1267
页数:15
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