Multitarget Strategies to Reduce Myocardial Ischemia/Reperfusion Injury JACC Review Topic of the Week

被引:498
|
作者
Davidson, Sean M. [1 ]
Ferdinandy, Peter [2 ,3 ]
Andreadou, Ioanna [4 ]
Botker, Hans Erik [5 ]
Heusch, Gerd [6 ]
Ibanez, Borja [7 ,8 ,9 ]
Ovize, Michel [10 ,11 ]
Schulz, Rainer [12 ]
Yellon, Derek M. [1 ]
Hausenloy, Derek J. [1 ,13 ,14 ,15 ,16 ]
Garcia-Dorado, David [9 ,17 ,18 ]
机构
[1] UCL, Hatter Cardiovasc Inst, 67 Chenies Mews, London WC1E 6HX, England
[2] Semmelweis Univ, Dept Pharmacol & Pharmacotherapy, Budapest, Hungary
[3] Pharmahungary Grp, Szeged, Hungary
[4] Natl & Kapodistrian Univ Athens, Fac Pharm, Lab Pharmacol, Athens, Greece
[5] Aarhus Univ Hosp Skejby, Dept Cardiol, Aarhus N, Denmark
[6] Univ Essen Gesamthsch, Med Sch, West German Heart & Vasc Ctr, Inst Pathophysiol, Essen, Germany
[7] Ctr Nacl Invest Cardiovasc Carlos III, Madrid, Spain
[8] CIBER Enfermedades CardioVasc, Madrid, Spain
[9] IIS Fdn Jimenez Diaz Univ Hosp, Madrid, Spain
[10] Univ Lyon, CarMeN Lab, INSERM, U1060, Lyon, France
[11] Hosp Civils Lyon, Hop Louis Pradel, Explorat Fonct Cardiovasc, Lyon, France
[12] Justus Liebig Univ Giessen, Inst Physiol, Giessen, Germany
[13] Duke Natl Univ Singapore, Med Sch, Cardiovasc & Metab Disorders Program, Singapore, Singapore
[14] Natl Heart Res Inst Singapore, Natl Heart Ctr, Singapore, Singapore
[15] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore, Singapore
[16] Tecnol Monterrey, Escuela Ingn & Ciencias, Ctr Biotecnol FEMSA, Nuevo Leon, Mexico
[17] Vall dHebron Univ Hosp & Res Inst VHIR, Vasc Biol & Metab Area, Dept Cardiol, Barcelona, Spain
[18] Univ Autonoma Barcelona, Barcelona, Spain
基金
英国医学研究理事会;
关键词
cardioprotection; ischemia; myocardial infarction; reperfusion; ST-SEGMENT-ELEVATION; ISCHEMIA-REPERFUSION INJURY; PERCUTANEOUS CORONARY INTERVENTION; INFARCT SIZE; EUROPEAN-SOCIETY; NITRIC-OXIDE; ENHANCES CARDIOPROTECTION; CELLULAR BIOLOGY; HYDROGEN-SULFIDE; WORKING GROUP;
D O I
10.1016/j.jacc.2018.09.086
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Many treatments have been identified that confer robust cardioprotection in experimental animal models of acute ischemia and reperfusion injury. However, translation of these cardioprotective therapies into the clinical setting of acute myocardial infarction (AMI) for patient benefit has been disappointing. One important reason might be that AMI is multifactorial, causing cardiomyocyte death via multiple mechanisms, as well as affecting other cell types, including platelets, fibroblasts, endothelial and smooth muscle cells, and immune cells. Many cardioprotective strategies act through common end-effectors and may be suboptimal in patients with comorbidities. In this regard, emerging data suggest that optimal cardioprotection may require the combination of additive or synergistic multitarget therapies. This review will present an overview of the state of cardioprotection today and provide a roadmap for how we might progress towards successful clinical use of cardioprotective therapies following AMI, focusing on the rational combination of judiciously selected, multitarget therapies. This paper emerged as part of the discussions of the European Union (EU)-CARDIOPROTECTION Cooperation in Science and Technology (COST) Action, CA16225. (c) 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:89 / 99
页数:11
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