Violi F, Alessandri C, Frattaroli S, Ghiselli A, Balsano F
Thromb Haemost. 1982 Oct 29;48(2):166-8.
A double blind study was performed on 20 atherosclerotic patients. A placebo was administered to one group of 10 patients (group A) and ticlopidine (500 mg/day) was administered to another group of 10 patients (group B) for one month. ADP and collagen-induced platelet aggregation (PA), platelet malondialdehyde (MDA) produced by thrombin stimulation and plasma beta-thromboglobulin (beta TG) levels, prothrombin time, activated partial thromboplastin time (APTT) fibrinogen, antithrombin (AT) III fibrin(ogen) degradation products, alpha 2-antiplasmin and plasminogen were evaluated in both groups before and after treatment. No changes in PA, MDA and beta TG were seen in group A. Group B showed a significant decrease of PA, beta TG and a significant increase of MDA. No changes on blood coagulation data were seen in either group. This study suggests that ticlopidine is able to inhibit platelet function in vivo.
对20名动脉粥样硬化患者进行了一项双盲研究。给一组10名患者(A组)服用安慰剂,给另一组10名患者(B组)服用噻氯匹定(500毫克/天),持续一个月。在治疗前后评估两组患者的二磷酸腺苷(ADP)和胶原诱导的血小板聚集(PA)、凝血酶刺激产生的血小板丙二醛(MDA)和血浆β-血小板球蛋白(β-TG)水平、凝血酶原时间、活化部分凝血活酶时间(APTT)、纤维蛋白原、抗凝血酶(AT)Ⅲ、纤维蛋白(原)降解产物、α2-抗纤溶酶和纤溶酶原。A组的PA、MDA和β-TG未见变化。B组的PA、β-TG显著降低,MDA显著升高。两组的凝血数据均未见变化。本研究表明,噻氯匹定能够在体内抑制血小板功能。