氧化应激
心肌保护
肾葡萄糖重吸收
活性氧
药理学
化学
平衡
医学
协同运输机
内皮功能障碍
葡萄糖稳态
内科学
达帕格列嗪
血糖性
内分泌学
2型糖尿病
糖尿病
生物化学
钠
胰岛素抵抗
缺血
有机化学
作者
Gloria M. Gager,Dirk von Lewinski,Harald Sourij,Bernd Jilma,Ceren Eyileten,Krzysztof Filipiak,Martin Hülsmann,Jacek Kubica,Marek Postuła,Jolanta M. Siller‐Matula
标识
DOI:10.1016/j.biopha.2021.112169
摘要
Sodium-glucose cotransporter 2 (SGLT2) inhibitors present a class of antidiabetic drugs, which inhibit renal glucose reabsorption resulting in the elevation of urinary glucose levels. Within the past years, SGLT2 inhibitors have become increasingly relevant due to their effects beyond glycemic control in patients with type 2 diabetes (T2DM). Although dedicated large trials demonstrated cardioprotective effects of SGLT2 inhibitors, the exact mechanisms responsible for those benefits have not been fully identified. Alterations in Ca2+ signaling and oxidative stress accompanied by excessive reactive oxygen species (ROS) production, fibrosis and inflammatory processes form cornerstones of potential molecular targets for SGLT2 inhibitors. This review focused on three hypotheses for SGLT2 inhibitor-mediated cardioprotection: ion homeostasis, oxidative stress and endothelial dysfunction.
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