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Sodium-Glucose Co-transporter-2 Inhibitor of Dapagliflozin Attenuates Myocardial Ischemia/Reperfusion Injury by Limiting NLRP3 Inflammasome Activation and Modulating Autophagy.达格列净的钠-葡萄糖协同转运蛋白2抑制剂通过限制NLRP3炎性小体激活和调节自噬减轻心肌缺血/再灌注损伤。
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Association of Sodium-Glucose Cotransporter 2 Inhibitors With Cardiovascular Outcomes in Patients With Type 2 Diabetes and Other Risk Factors for Cardiovascular Disease: A Meta-analysis.钠-葡萄糖共转运蛋白 2 抑制剂与 2 型糖尿病及其他心血管疾病危险因素患者心血管结局的相关性:一项荟萃分析。
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Guidelines for in vivo mouse models of myocardial infarction.心肌梗死体内小鼠模型的指南。
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Sodium-Glucose Cotransporter 2 Inhibitors, All-Cause Mortality, and Cardiovascular Outcomes in Adults with Type 2 Diabetes: A Bayesian Meta-Analysis and Meta-Regression.钠-葡萄糖共转运蛋白 2 抑制剂在 2 型糖尿病成人患者中的全因死亡率和心血管结局:贝叶斯荟萃分析和荟萃回归。
J Am Heart Assoc. 2021 Sep 21;10(18):e019918. doi: 10.1161/JAHA.120.019918. Epub 2021 Sep 13.
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Cardioprotective effects of empagliflozin after ischemia and reperfusion in rats.依帕格列净对大鼠缺血再灌注后的心脏保护作用。
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Sodium-glucose cotransporter 2 inhibitors reduce myocardial infarct size in preclinical animal models of myocardial ischaemia-reperfusion injury: a meta-analysis.钠-葡萄糖共转运蛋白 2 抑制剂可减少心肌缺血再灌注损伤的临床前动物模型中的心肌梗死面积:一项荟萃分析。
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2型糖尿病的新治疗选择及其对缺血性心脏病的影响。

New Therapeutic Options for Type 2 Diabetes Mellitus and Their Impact Against Ischemic Heart Disease.

作者信息

Almutairi Malak, Chan Jordan S F, Ussher John R

机构信息

Saudi Food and Drug Authority, Riyadh, Saudi Arabia.

Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, AB, Canada.

出版信息

Front Physiol. 2022 Jun 27;13:904626. doi: 10.3389/fphys.2022.904626. eCollection 2022.

DOI:10.3389/fphys.2022.904626
PMID:35832485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9271769/
Abstract

Type 2 diabetes mellitus (T2DM) greatly increases risk for cardiovascular disease, including ischemic heart disease and myocardial infarction. With the completion of several cardiovascular outcomes trials (CVOTs) for new glucose-lowering therapies, including the sodium-glucose cotransporter-2 (SGLT2) inhibitors and glucagon-like peptide-1 receptor (GLP-1R) agonists, we now have strong evidence alluding to the cardioprotective nature of these agents in people with T2DM. These agents have frequently been observed to reduce rates for 3-point major adverse cardiovascular events, which encompass death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. Herein we will provide an overview on whether reductions in nonfatal myocardial infarction and ischemic heart disease status are a key component of the improved cardiovascular outcomes in people with T2DM treated with either SGLT2 inhibitors or GLP-1R agonists. Observations from preclinical studies will be compared to their clinical counterparts, while being further interrogated to define potential mechanisms that may account for SGLT2 inhibitor or GLP-1R agonist-induced cardioprotection against ischemic heart disease. A better understanding of the role these agents have in impacting the progression of ischemic heart disease in individuals with T2DM will have a substantial impact in our management of this patient population.

摘要

2型糖尿病(T2DM)会大幅增加心血管疾病的风险,包括缺血性心脏病和心肌梗死。随着多项针对新型降糖疗法的心血管结局试验(CVOT)的完成,包括钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂和胰高血糖素样肽-1受体(GLP-1R)激动剂,我们现在有充分证据表明这些药物对T2DM患者具有心脏保护作用。这些药物经常被观察到能降低3点主要不良心血管事件的发生率,这些事件包括心血管原因导致的死亡、非致命性心肌梗死或非致命性中风。在此,我们将概述非致命性心肌梗死和缺血性心脏病状况的改善是否是使用SGLT2抑制剂或GLP-1R激动剂治疗的T2DM患者心血管结局改善的关键组成部分。将临床前研究的观察结果与其临床对应结果进行比较,同时进一步探究可能解释SGLT2抑制剂或GLP-1R激动剂诱导的针对缺血性心脏病的心脏保护作用的潜在机制。更好地理解这些药物在影响T2DM患者缺血性心脏病进展中所起的作用,将对我们管理这一患者群体产生重大影响。