Bing R J
Cardiovasc Res. 2001 Jul;51(1):13-20. doi: 10.1016/s0008-6363(01)00250-4.
This report reviews the author's involvement in the growth of ideas and basic concepts in myocardial ischemia resulting in the histological changes of myocardial infarction. Concepts arising from the study of myocardial substrate utilization, activation of the inducible form of nitric oxide synthase and production of prostacyclin and thromboxane in the infarcted heart are presented. New approaches are discussed dealing with the effects of nonsteroidal anti-inflammatory drugs on myocardial production of nitric oxide and prostanoids, and with the relevance of the inducible form of cyclooxygenase. The review also records a number of significant similarities between angiogenesis in the ischemic heart and some cancers. Angiogenesis in both instances originates from inflammatory reactions, illustrating how different tissues and organs such as ischemic heart muscle and cancer react to similar pathological stimuli in an identical manner. This multifocal approach opens new concepts on myocardial ischemia and cancer.
本报告回顾了作者在心肌缺血相关思想和基本概念发展过程中的参与情况,这些思想和概念导致了心肌梗死的组织学变化。文中介绍了心肌底物利用研究、诱导型一氧化氮合酶的激活以及梗死心脏中前列环素和血栓素的产生所引发的概念。讨论了处理非甾体抗炎药对心肌一氧化氮和前列腺素产生的影响以及诱导型环氧化酶相关性的新方法。该综述还记录了缺血性心脏血管生成与某些癌症之间的一些显著相似之处。在这两种情况下,血管生成均源于炎症反应,说明了诸如缺血性心肌和癌症等不同组织和器官如何以相同方式对相似的病理刺激做出反应。这种多焦点方法为心肌缺血和癌症带来了新的概念。