In vivo models of myocardial ischemia and reperfusion injury - Application to drug discovery and evaluation

被引:29
作者
Black, SC [1 ]
机构
[1] Pfizer Inc, Global Res & Dev, Dept Cardiovasc & Metab Dis, Groton, CT 06340 USA
关键词
ischemia; reperfusion; neutrophil; sodium-hydrogen exchange; in vivo; infarct size; adenosine;
D O I
10.1016/S1056-8719(00)00102-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review discusses the pharmacology of regional myocardial ischemia and reperfusion (I/R) injury and the utilization of in vivo animal models in the preclinical development of novel therapeutic compounds. The manuscript aims to provide an overview of a number of different cardioprotective strategies that have been successful from a preclinical perspective and to also present where possible results of clinical trials of the respective compounds. Myocardial ischemia reperfusion injury may be manifested as myocardial stunning, ventricular arrhythmias, coronary vascular dysfunction, or the development of a myocardial infarct. This review is principally concerned with preclinical studies related to reduction of infarct size. The pathophysiology of the reperfusion injury process is complex, including primarily cellular and humoral components of inflammation, as well as myocellular ionic and metabolic disturbances. This review will discuss strategies directed at oxygen-derived free radicals, neutrophils, adenosine, and the sodium-hydrogen exchanger (NHE). The results of preclinical cardioprotective studies are influenced by the paradigm used therefore methodological considerations will also be presented where appropriate. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:153 / 167
页数:15
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