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保存再灌注心肌的新方法和新视角。

New and revisited approaches to preserving the reperfused myocardium.

机构信息

Cardiovascular Research Institute, Huntington Medical Research Institutes, 99 North El Molino Avenue, Pasadena, California 91101, USA.

Division of Cardiovascular Medicine and Department of Medicine, Keck School of Medicine, University of Southern California, 1975 Zonal Avenue, Los Angeles, California 90033, USA.

出版信息

Nat Rev Cardiol. 2017 Nov;14(11):679-693. doi: 10.1038/nrcardio.2017.102. Epub 2017 Jul 27.

DOI:10.1038/nrcardio.2017.102
PMID:28748958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5991096/
Abstract

Early coronary artery reperfusion improves outcomes for patients with ST-segment elevation myocardial infarction (STEMI), but morbidity and mortality after STEMI remain unacceptably high. The primary deficits seen in these patients include inadequate pump function, owing to rapid infarction of muscle in the first few hours of treatment, and adverse remodelling of the heart in the months that follow. Given that attempts to further reduce myocardial infarct size beyond early reperfusion in clinical trials have so far been disappointing, effective therapies are still needed to protect the reperfused myocardium. In this Review, we discuss several approaches to preserving the reperfused heart, such as therapies that target the mechanisms involved in mitochondrial bioenergetics, pyroptosis, and autophagy, as well as treatments that harness the cardioprotective properties of inhaled anaesthetic agents. We also discuss potential therapies focused on correcting the no-reflow phenomenon and its effect on healing and adverse left ventricular remodelling.

摘要

早期冠状动脉再灌注可改善 ST 段抬高型心肌梗死(STEMI)患者的预后,但 STEMI 患者的发病率和死亡率仍然高得令人无法接受。这些患者的主要缺陷包括泵功能不足,这是由于在治疗的最初几个小时内肌肉迅速梗死,以及在随后的几个月中心脏发生不良重塑。鉴于在临床试验中,试图在早期再灌注的基础上进一步减少心肌梗死面积的尝试迄今令人失望,因此仍然需要有效的治疗方法来保护再灌注的心肌。在这篇综述中,我们讨论了几种保护再灌注心脏的方法,例如针对线粒体生物能学、细胞焦亡和自噬相关机制的治疗方法,以及利用吸入麻醉剂的心脏保护特性的治疗方法。我们还讨论了一些潜在的治疗方法,这些方法侧重于纠正无复流现象及其对愈合和不良左心室重塑的影响。

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本文引用的文献

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The Highly Selective Caspase-1 Inhibitor VX-765 Provides Additive Protection Against Myocardial Infarction in Rat Hearts When Combined With a Platelet Inhibitor.高选择性半胱天冬酶-1抑制剂VX-765与血小板抑制剂联合使用时,对大鼠心脏心肌梗死具有额外的保护作用。
J Cardiovasc Pharmacol Ther. 2017 Nov;22(6):574-578. doi: 10.1177/1074248417702890. Epub 2017 Apr 12.
2
Ischemic postconditioning during primary percutaneous coronary intervention.初次经皮冠状动脉介入治疗期间的缺血后适应
Catheter Cardiovasc Interv. 2017 Dec 1;90(7):1059-1067. doi: 10.1002/ccd.26965. Epub 2017 Mar 15.
3
Meta-analysis of remote ischemic conditioning in patients with acute myocardial infarction.急性心肌梗死患者的远程缺血预处理的荟萃分析。
Sci Rep. 2017 Mar 8;7:43529. doi: 10.1038/srep43529.
4
The effects of remote ischemic conditioning in patients with ST-segment elevation myocardial infarction treated with primary percutaneous coronary intervention: a meta-analysis.远程缺血预处理对接受直接经皮冠状动脉介入治疗的ST段抬高型心肌梗死患者的影响:一项荟萃分析。
Minerva Med. 2017 Aug;108(4):370-380. doi: 10.23736/S0026-4806.17.04631-6. Epub 2017 Feb 17.
5
Silica nanoparticles induce cardiotoxicity interfering with energetic status and Ca handling in adult rat cardiomyocytes.二氧化硅纳米颗粒通过干扰成年大鼠心肌细胞的能量状态和钙处理诱导心脏毒性。
Am J Physiol Heart Circ Physiol. 2017 Apr 1;312(4):H645-H661. doi: 10.1152/ajpheart.00564.2016. Epub 2017 Jan 27.
6
Meta-Analysis of Randomized Trials on Remote Ischemic Conditioning During Primary Percutaneous Coronary Intervention in Patients With ST-Segment Elevation Myocardial Infarction.ST段抬高型心肌梗死患者直接经皮冠状动脉介入治疗期间远程缺血预处理的随机试验的Meta分析
Am J Cardiol. 2017 Mar 15;119(6):832-838. doi: 10.1016/j.amjcard.2016.11.036. Epub 2016 Dec 21.
7
Pharmacological Inhibition of NLRP3 Inflammasome Attenuates Myocardial Ischemia/Reperfusion Injury by Activation of RISK and Mitochondrial Pathways.NLRP3炎性小体的药理学抑制通过激活RISK和线粒体途径减轻心肌缺血/再灌注损伤
Oxid Med Cell Longev. 2016;2016:5271251. doi: 10.1155/2016/5271251. Epub 2016 Dec 8.
8
Therapeutic microparticles functionalized with biomimetic cardiac stem cell membranes and secretome.功能化的治疗性微颗粒,具有仿生心脏干细胞膜和分泌组。
Nat Commun. 2017 Jan 3;8:13724. doi: 10.1038/ncomms13724.
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Expert consensus document: Mitochondrial function as a therapeutic target in heart failure.专家共识文件:心力衰竭中作为治疗靶点的线粒体功能。
Nat Rev Cardiol. 2017 Apr;14(4):238-250. doi: 10.1038/nrcardio.2016.203. Epub 2016 Dec 22.
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J Thorac Cardiovasc Surg. 2017 Apr;153(4):934-943. doi: 10.1016/j.jtcvs.2016.10.077. Epub 2016 Nov 15.