Uchiyama S, Yamazaki M, Maruyama S
Department of Neurology, Tokyo Women's Medical College.
Nihon Rinsho. 1992 Feb;50(2):372-8.
Clopidogrel is a new thieno-pyridine derivative and has a more potent inhibitory effect on platelet aggregation, dependent on ADP rather than ticlopidine. In a phase I study performed in Japan, significant inhibition of ADP-induced platelet aggregation and prolongation of bleeding time was observed in the dose range of 25, 50 and 75 mg. These effects were comparable to 200 or 300 mg of ticlopidine. Antithrombotic effects have also been shown in experimental animal models. Clopidogrel is expected to reduce the incidence of neutropenia since smaller doses are sufficient to suppress platelet aggregation compared to ticlopidine. Clopidogrel has been proven to be a potent and well-tolerated antiplatelet agent for atherosclerosis patients at risk of thrombosis, in Europe.
氯吡格雷是一种新型噻吩并吡啶衍生物,对血小板聚集具有更强的抑制作用,其作用依赖于二磷酸腺苷(ADP),而非噻氯匹定。在日本进行的一项I期研究中,在25、50和75毫克的剂量范围内观察到对ADP诱导的血小板聚集有显著抑制作用,且出血时间延长。这些作用与200或300毫克噻氯匹定相当。在实验动物模型中也已显示出抗血栓形成作用。由于与噻氯匹定相比,较小剂量的氯吡格雷就足以抑制血小板聚集,因此预计氯吡格雷可降低中性粒细胞减少症的发生率。在欧洲,氯吡格雷已被证明是一种对有血栓形成风险的动脉粥样硬化患者有效的、耐受性良好的抗血小板药物。