The Hatter Cardiovascular Institute, University College London, 67 Chenies Mews, London, United Kingdom.
Antioxid Redox Signal. 2011 Mar 1;14(5):893-907. doi: 10.1089/ars.2010.3360. Epub 2010 Oct 26.
The discovery of ischemic postconditioning (IPost) has rejuvenated the field of cardioprotection. As an interventional strategy to be applied at the onset of myocardial reperfusion, the transition of IPost from a bench-side curiosity to potential clinical therapy has been impressively rapid. Its existence also confirms the existence of lethal myocardial reperfusion injury in man, suggesting that 40%-50% of the final reperfused myocardial infarct may actually be due to myocardial reperfusion injury. Intensive analysis of the signal transduction pathways underlying IPost has identified similarities with the signaling pathways underlying its preischemic counterpart, ischemic preconditioning. In this article, the reperfusion injury salvage kinase pathway and the more recently described survivor activating factor enhancement pathway, two apparently distinct signaling pathways that actually interact to convey the IPost stimulus from the cell surface to the mitochondria, where many of the prosurvival and death signals appear to converge. The elucidation of the reperfusion signaling pathways underlying IPost may result in the identification of novel pharmacological targets for cardioprotection.
缺血后适应(IPost)的发现使心肌保护领域重获生机。作为一种在心肌再灌注开始时应用的介入策略,IPost 从一个实验台上的好奇事物迅速转变为潜在的临床治疗方法。它的存在也证实了人类存在致命性心肌再灌注损伤,这表明最终再灌注心肌梗死的 40%-50%实际上可能是由于心肌再灌注损伤引起的。对 IPost 相关信号转导通路的深入分析表明,其与缺血预处理的信号通路相似。在本文中,再灌注损伤挽救激酶通路和最近描述的存活激活因子增强通路,这两种明显不同的信号通路实际上相互作用,将 IPost 刺激从细胞膜传递到线粒体,许多生存和死亡信号似乎在那里汇聚。阐明 IPost 相关的再灌注信号通路可能会发现新的心肌保护药理学靶点。