Sasaki Y, Ishii I, Giddings J C, Yamamoto J
Laboratory of Physiology, Faculty of Nutrition, Kobe Gakuin University, Japan.
Haemostasis. 1996 May-Jun;26(3):150-6. doi: 10.1159/000217200.
The protective effects of ticlopidine and d,l-lysine acetylsalicylate (L-ASA), used alone and in combination, on the pathogenesis of thrombosis in cerebral blood vessels were investigated in a rat animal model using a He-Ne laser method. Ticlopidine and L-ASA, given orally at a concentration from 100 mg/kg, inhibited thrombus formation in a dose-dependent manner. Ticlopidine (300 mg/kg p.o.) inhibited thrombosis in arterioles and venules for 3 days after administration. The inhibitory activity of L-ASA (300 mg/kg p.o.) was less prolonged than that of ticlopidine and was observed for only approximately 24 h. Combined administration of ticlopidine and L-ASA significantly enhanced and prolonged the antithrombotic effects of either drug given alone. The results demonstrate that ticlopidine and L-ASA have potent antithrombotic properties in rat cerebral blood vessels in vivo.
在大鼠动物模型中,采用氦氖激光法研究了噻氯匹定和消旋赖氨酸乙酰水杨酸酯(L-ASA)单独使用及联合使用对脑血管血栓形成发病机制的保护作用。噻氯匹定和L-ASA以100mg/kg的浓度口服给药,呈剂量依赖性抑制血栓形成。噻氯匹定(300mg/kg口服)给药后3天抑制小动脉和小静脉血栓形成。L-ASA(300mg/kg口服)的抑制活性持续时间比噻氯匹定短,仅观察到约24小时。噻氯匹定和L-ASA联合给药显著增强并延长了单独使用任一药物的抗血栓作用。结果表明,噻氯匹定和L-ASA在大鼠体内脑血管中具有强大的抗血栓特性。