AtheroThrombosis Research Unit, Cardiovascular Institute, Mount Sinai School of Medicine, New York, New York 10029, USA.
Thromb Haemost. 2010 Nov;104(5):949-54. doi: 10.1160/TH10-03-0195. Epub 2010 Sep 30.
Atherosclerosis and its clinical manifestations (i.e. myocardial infarction, stroke) are major causes of mortality and morbidity in Western countries. Endothelial dysfunction is considered the first step in the cascade leading up to coronary events. Increasing evidence suggests that direct inhibition of thromboxane A2/prostaglandin (TP)-receptors may not only have anti-platelet effects but also impact endothelial dysfunction as well as inflammatory component of atherosclerosis. While TP-receptor involvement in platelet function has received the greatest attention, more recent findings support the critical role of TP-receptor in other pathophysiological aspects of atherothrombosis. Prostanoids (i.e. TxA2, F2-isoprostanes, prostaglandins endoperoxides PGG2/PGH2) are known to promote the initiation and progression of atherosclerosis, not only via platelet activation, but through leukocyte-endothelial interactions and vasoconstriction. Dysfunctional endothelium, characterised by increased COX-activity, releases prostanoids that promote endothelial exposure to adhesion molecules and induce smooth muscle cell contraction. Plaque macrophages synthesise PGH2/PGG2 via COX-2; these potent prostanoids can trigger platelet activation and aggregation despite COX-1 inhibition by aspirin. TP-receptor inhibition has been reported to exert anti-atherosclerotic effects in pre-clinical model of disease. Reduction of plaque burden was associated with plaque stabilisation documented by the reduction in the content of macrophages, apoptotic cells, MMPs and endothelin-1, and the increase in smooth muscle cells content. TP-receptor blockade might have an anti-atherosclerotic and plaque stabilisation effect. The possibility of combining anti-platelet activity with an anti-atherosclerotic effect via selective TP-receptor inhibitors could have important implications especially in clinical conditions associated with increased production of prostanoids, such as diabetes.
动脉粥样硬化及其临床表现(如心肌梗死、中风)是西方国家死亡率和发病率的主要原因。内皮功能障碍被认为是导致冠状动脉事件级联反应的第一步。越来越多的证据表明,直接抑制血栓素 A2/前列腺素(TP)受体不仅具有抗血小板作用,而且还可以影响内皮功能障碍以及动脉粥样硬化的炎症成分。虽然 TP 受体在血小板功能中的作用受到了最大的关注,但最近的研究结果支持 TP 受体在动脉血栓形成的其他病理生理方面的关键作用。前列腺素(如血栓素 A2、F2-异前列腺素、前列腺素内过氧化物 PGG2/PGH2)已知可促进动脉粥样硬化的起始和进展,不仅通过血小板激活,还通过白细胞-内皮相互作用和血管收缩。功能失调的内皮细胞,其特征是 COX 活性增加,释放促进内皮暴露于粘附分子并诱导平滑肌细胞收缩的前列腺素。斑块巨噬细胞通过 COX-2 合成 PGH2/PGG2;这些强效前列腺素可以触发血小板激活和聚集,尽管 COX-1 被阿司匹林抑制。据报道,TP 受体抑制在疾病的临床前模型中具有抗动脉粥样硬化作用。斑块负荷的减少与斑块稳定性有关,这可通过减少巨噬细胞、凋亡细胞、基质金属蛋白酶和内皮素-1的含量以及增加平滑肌细胞含量来证明。TP 受体阻断可能具有抗动脉粥样硬化和斑块稳定作用。通过选择性 TP 受体抑制剂将抗血小板活性与抗动脉粥样硬化作用相结合的可能性具有重要意义,特别是在与前列腺素产生增加相关的临床情况下,如糖尿病。