Department of Internal Medicine-Medical Semiotics, "Victor Babeș" University of Medicine and Pharmacy of Timișoara, E. Murgu Sq. No. 2, 300041 Timișoara, Romania.
Doctoral School Medicine-Pharmacy, "Victor Babeș" University of Medicine and Pharmacy of Timișoara, E. Murgu Sq., No. 2, 300041 Timișoara, Romania.
Int J Mol Sci. 2024 Jul 14;25(14):7711. doi: 10.3390/ijms25147711.
Sodium-glucose cotransporter 2 inhibitors (SGLT2i), a novel class of glucose-lowering drugs, have revolutionized the management of heart failure with reduced and preserved ejection fraction, regardless of the presence of diabetes, and are currently incorporated in the heart failure guidelines. While these drugs have consistently demonstrated their ability to decrease heart failure hospitalizations in several landmark clinical trials, their cardioprotective effects are far from having been completely elucidated. In the past decade, a growing body of experimental research has sought to address the molecular and cellular mechanisms of SGLT2i in order to provide a better understanding of the off-target acute and chronic cardiac benefits, beyond the on-target renal effect responsible for blood glucose reduction. The present narrative review addresses the direct cardioprotective effects of SGLT2i, delving into the off-target mechanisms of the drugs currently approved for heart failure therapy, and provides insights into future perspectives.
钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)是一类新型的降糖药物,无论是否患有糖尿病,它都彻底改变了射血分数降低和保留的心力衰竭的治疗方法,目前已被纳入心力衰竭指南。虽然这些药物在几项具有里程碑意义的临床试验中一致证明了它们能够降低心力衰竭住院率,但它们的心脏保护作用还远未完全阐明。在过去的十年中,越来越多的实验研究试图阐明 SGLT2i 的分子和细胞机制,以便更好地了解除了负责降低血糖的靶肾效应之外的药物的非靶急性和慢性心脏益处。本综述探讨了 SGLT2i 的直接心脏保护作用,深入研究了目前批准用于心力衰竭治疗的药物的非靶机制,并为未来的研究提供了新的视角。