Kim Y S, Pyo M K, Park K M, Park P H, Hahn B S, Wu S J, Yun-Choi H S
Natural Products Research Institute, Seoul National University, Korea.
Thromb Res. 1998 Jul 1;91(1):33-8. doi: 10.1016/s0049-3848(98)00075-9.
The antiplatelet and antithrombotic effects of the oral combination treatment of ticlopidine and Ginkgo biloba extract (EGb 761) were studied in normal and thrombosis-induced rats. The ex vivo inhibitory effect on ADP-induced platelet aggregation of a small dose of ticlopidine (50 mg/kg/day) in combination with EGb 761 (40 mg/kg/day) was comparable to a larger dose of only ticlopidine (200 mg/kg/day). Bleeding time was also prolonged by 150%. Thrombus weight was also consistently decreased by a combination of ticlopidine and EGb 761 in an arterio-venous shunt model at two doses of ticlopidine (50 mg/kg) plus EGb 761 (20 mg/kg) and ticlopidine (50 mg/kg) plus EGb 761 (40 mg/kg). A combinatory treatment in acute thrombosis model in mice also showed a higher recovery than a single treatment.
在正常大鼠和诱导血栓形成的大鼠中研究了噻氯匹定与银杏叶提取物(EGb 761)联合口服治疗的抗血小板和抗血栓形成作用。小剂量噻氯匹定(50毫克/千克/天)与EGb 761(40毫克/千克/天)联合使用时,对ADP诱导的血小板聚集的体外抑制作用与较大剂量的单独噻氯匹定(200毫克/千克/天)相当。出血时间也延长了150%。在动静脉分流模型中,两种剂量的噻氯匹定(50毫克/千克)加EGb 761(20毫克/千克)以及噻氯匹定(50毫克/千克)加EGb 761(40毫克/千克)联合使用时,血栓重量也持续降低。在小鼠急性血栓形成模型中的联合治疗也显示出比单一治疗更高的恢复率。