Second Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1 West-16, Sapporo 060-8543, Japan.
Cardiovasc Diabetol. 2012 Jun 13;11:67. doi: 10.1186/1475-2840-11-67.
In spite of the current optimal therapy, the mortality of patients with ischemic heart disease (IHD) remains high, particularly in cases with diabetes mellitus (DM) as a co-morbidity. Myocardial infarct size is a major determinant of prognosis in IHD patients, and development of a novel strategy to limit infarction is of great clinical importance. Ischemic preconditioning (PC), postconditioning (PostC) and their mimetic agents have been shown to reduce infarct size in experiments using healthy animals. However, a variety of pharmacological agents have failed to demonstrate infarct size limitation in clinical trials. One of the possible reasons for the discrepancy between the results of animal experiments and clinical trials is that co-morbidities, including DM, modified myocardial responses to ischemia/reperfusion and to cardioprotective agents. Here we summarize observations of the effects of DM on myocardial infarct size and ischemic PC and PostC and discuss perspectives for protection of DM hearts.
尽管目前的治疗方法最佳,但缺血性心脏病(IHD)患者的死亡率仍然很高,特别是在合并糖尿病(DM)的情况下。心肌梗死面积是 IHD 患者预后的主要决定因素,开发一种限制梗死的新策略具有重要的临床意义。缺血预处理(PC)、后处理(PostC)及其模拟剂已被证明可减少健康动物实验中的梗死面积。然而,许多药物在临床试验中未能证明梗死面积的限制。动物实验结果与临床试验结果不一致的一个可能原因是合并症,包括糖尿病,改变了心肌对缺血/再灌注和心脏保护剂的反应。在这里,我们总结了 DM 对心肌梗死面积和缺血性 PC 和 PostC 的影响的观察结果,并讨论了保护 DM 心脏的前景。