Gkaliagkousi Eugenia, Ritter James, Ferro Albert
Department of Clinical Pharmacology, Cardiovascular Division, School of Medicine, King's College London, London SE1 9NH, UK.
Circ Res. 2007 Sep 28;101(7):654-62. doi: 10.1161/CIRCRESAHA.107.158410.
Nitric oxide (NO) exerts important vasodilatory, antiplatelet, antioxidant, antiadhesive, and antiproliferative effects. Although endothelium derived NO has been shown to be of prime importance in cardio- and vasculoprotection, until recently little was known about the role of platelet-derived NO. New evidence suggests that NO synthesized by platelets regulates platelet functions, in particular suppressing platelet activation and intravascular thrombosis. Moreover, platelet NO biosynthesis may be decreased in patients with cardiovascular risk factors or with coronary heart disease, and this may contribute to arterial thrombotic disease in these patients. Here, we review the current state of knowledge as regards the role of platelet-derived NO, both in normal physiology and in cardiovascular disease states, and compare platelet NO signaling and regulation with that in endothelial cells.
一氧化氮(NO)具有重要的血管舒张、抗血小板、抗氧化、抗黏附和抗增殖作用。尽管内皮源性NO已被证明在心脏和血管保护中至关重要,但直到最近,关于血小板源性NO的作用仍知之甚少。新证据表明,血小板合成的NO调节血小板功能,特别是抑制血小板活化和血管内血栓形成。此外,有心血管危险因素或冠心病患者的血小板NO生物合成可能减少,这可能导致这些患者发生动脉血栓性疾病。在此,我们综述了血小板源性NO在正常生理和心血管疾病状态中的作用的当前知识状态,并将血小板NO信号传导和调节与内皮细胞中的进行比较。