Department of Cardiology, the Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Key Laboratory of Medical Electrophysiology of Ministry of Education and Medical Electrophysiological Key Laboratory of Sichuan Province, Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease, Institute of Cardiovascular Research, Southwest Medical University, Luzhou, 646000, Sichuan, China.
J Cardiovasc Transl Res. 2024 Oct;17(5):1018-1035. doi: 10.1007/s12265-024-10513-x. Epub 2024 May 20.
Ischemic heart disease (IHD) is a common clinical cardiovascular disease with high morbidity and mortality. Sodium glucose cotransporter protein inhibitor (SGLTi) is a novel hypoglycemic drug. To date, both clinical trials and animal experiments have shown that SGLTi play a protective role in IHD, including myocardial infarction (MI) and ischemia/reperfusion (I/R). The protective effects may be involved in mechanisms of energy metabolic conversion, anti-inflammation, anti-fibrosis, ionic homeostasis improvement, immune cell development, angiogenesis and functional regulation, gut microbiota regulation, and epicardial lipids. Thus, this review summarizes the above mechanisms and aims to provide theoretical evidence for therapeutic strategies for IHD.
缺血性心脏病(IHD)是一种常见的临床心血管疾病,具有较高的发病率和死亡率。钠-葡萄糖共转运蛋白抑制剂(SGLTi)是一种新型的降糖药物。迄今为止,临床试验和动物实验均表明 SGLTi 在缺血性心脏病(包括心肌梗死(MI)和缺血/再灌注(I/R))中发挥保护作用。这种保护作用可能涉及能量代谢转换、抗炎、抗纤维化、离子稳态改善、免疫细胞发育、血管生成和功能调节、肠道微生物群调节和心外膜脂质等机制。因此,本综述总结了上述机制,旨在为 IHD 的治疗策略提供理论依据。