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超越再灌注治疗保护急性缺血心肌:我们距离实现消除梗死面积的梦想更近了吗?

Protecting the acutely ischemic myocardium beyond reperfusion therapies: are we any closer to realizing the dream of infarct size elimination?

作者信息

Tissier R, Cohen M V, Downey J M

机构信息

Ecole nationale vétérinaire d'Alfort, Maisons-Alfort.

出版信息

Arch Mal Coeur Vaiss. 2007 Sep;100(9):794-802.

Abstract

Patients currently treated for acute myocardial infarction receive reperfusion therapy as their only anti-infarct intervention. Although pharmacologic agents have been evaluated in the past for their ability to salvage ischemic myocardium when administered at reperfusion, until very recently none has demonstrated clear efficacy in clinical trials. However, a new generation of interventions has emerged which protects the heart by activating the reperfusion-induced salvage kinase (RISK) pathway. Unlike the disappointing results documented with previously touted putative cardioprotective agents, the preclinical experience with these newer interventions is very consistent indicating that there is a high likelihood that they will be effective clinically. Ischemic postconditioning, which also acts by activating the RISK pathway, has shown marked reduction in infarct size in small-scale trials. Finally, if a strategy for rapidly cooling the heart can be devised so that the in-hospital normothermic ischemic time can be significantly reduced, then infarct size can be even further decreased. In our opinion it is well within our reach using existing technologies to see the day when infarction can be virtually eliminated in the patient with acute coronary occlusion.

摘要

目前接受急性心肌梗死治疗的患者将再灌注治疗作为其唯一的抗梗死干预措施。尽管过去曾评估过药物在再灌注时挽救缺血心肌的能力,但直到最近,尚无药物在临床试验中显示出明确疗效。然而,新一代干预措施已经出现,这些措施通过激活再灌注诱导的挽救激酶(RISK)途径来保护心脏。与先前备受吹捧的假定心脏保护剂所记录的令人失望的结果不同,这些新干预措施的临床前经验非常一致,表明它们在临床上很有可能有效。缺血后处理同样通过激活RISK途径起作用,在小规模试验中已显示梗死面积显著减小。最后,如果能够设计出一种快速冷却心脏的策略,从而显著缩短院内常温缺血时间,那么梗死面积甚至可以进一步减小。我们认为,利用现有技术,我们完全有可能看到急性冠状动脉闭塞患者几乎能够消除梗死的那一天。

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