Protease-activated receptors in cardiovascular health and diseases

被引:46
作者
Shah, Rahman [1 ]
机构
[1] Baylor Coll Med, Texas Heart Ctr, Off Clin Res, Dept Cardiovasc Med, Houston, TX 77030 USA
关键词
THROMBIN-RECEPTOR; ANTIPLATELET THERAPY; PLATELET ACTIVATION; MEDIATED MECHANISM; ANTAGONISTS; METAANALYSIS; INHIBITION; EXPRESSION; DISCOVERY; CELLS;
D O I
10.1016/j.ahj.2008.09.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Platelet, once thought to be solely involved in clot formation, is now known to be a key mediator in various other processes such as inflammation, thrombosis, and atherosclerosis. Therefore, antiplatelet agents have become paramount in the prevention and management of various cardiovascular diseases. However, the currently most widely used antiplatelet drugs, aspirin and clopidogrel, have been shown to reduce the risk of serious vascular events only by approximately one quarter. Similarly, oral glycoprotein llb/Illa antagonists have been associated with excess mortality, thus restricting the use of parental glycoprotein llb/Illa antagonists to the treatment of acute clinical conditions. Thus, for the prevention of cardiovascular diseases, there is still a clinical need for antiplatelet drugs with higher antithrombotic efficacy but with safety profiles that allow for a preventive long-term administration. Thrombin signaling through the protease-activated receptors (PARs) has been shown to influence a wide range of physiologic and pathologic responses in cardiovascular systems. Thus, interference with PARs appears to be a promising strategy to develop new antiplatelet agents with higher efficacy. This review focuses on the cardiovascular actions of PARS that play a role in normal cardiovascular physiology and that are likely to contribute to cardiovascular diseases. (Am Heart J 2009; 157:253-62.)
引用
收藏
页码:253 / 262
页数:10
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