恩帕吉菲
尿钠
后负荷
心力衰竭
医学
脂肪因子
背景(考古学)
利尿
糖尿病
内科学
药理学
2型糖尿病
内分泌学
肾
血压
生物
胰岛素抵抗
古生物学
作者
Subodh Verma,John J.V. McMurray
出处
期刊:Diabetologia
[Springer Science+Business Media]
日期:2018-07-20
卷期号:61 (10): 2108-2117
被引量:730
标识
DOI:10.1007/s00125-018-4670-7
摘要
Sodium-glucose cotransporter (SGLT)2 inhibitors have been demonstrated to reduce cardiovascular events, particularly heart failure, in cardiovascular outcome trials. Here, we review the proposed mechanistic underpinnings of this benefit. Specifically, we focus on the role of SGLT2 inhibitors in optimising ventricular loading conditions through their effect on diuresis and natriuresis, in addition to reducing afterload and improving vascular structure and function. Further insights into the role of SGLT2 inhibition in myocardial metabolism and substrate utilisation are outlined. Finally, we discuss two emerging themes: how SGLT2 inhibitors may regulate Na+/H+ exchange at the level of the heart and kidney and how they may modulate adipokine production. The mechanistic discussion is placed in the context of completed and ongoing trials of SGLT2 inhibitors in the prevention and treatment of heart failure in individuals with and without diabetes.
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