Aoki T, Cox D, Senzaki K, Seki J, Tanaka A, Takasugi H, Motoyama Y
Department of Pharmacology, New Drug Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
Thromb Res. 1998 Feb 1;89(3):129-36. doi: 10.1016/s0049-3848(97)00308-3.
Antiplatelet and antithrombotic effects of FK633 (a GPIIb/IIIa antagonist) and aspirin were compared. FK633 at 0.32 mg/kg i.v. or aspirin at 10 mg/ kg i.v. inhibited ex vivo collagen-induced aggregation by >50% for 1 hour in guinea pigs. However, aspirin was very weak in inhibiting ADP-induced aggregation. In vivo antithrombotic effects of FK633 and aspirin were compared using a FeCl3-induced carotid artery thrombosis model in guinea pigs. Pretreatment with 0.32 mg/kg i.v. of FK633 significantly prevented occlusive thrombus formation, but aspirin at 10 mg/kg i.v. did not. In thrombolysis experiments, adjunctive use of FK633 (0.32 mg/kg i.v.) with rt-PA (0.3 mg/kg bolus+1.0 mg/kg/hr) achieved reperfusion in five of five animals without reocclusion. Aspirin (10O mg/kg i.v.) with rt-PA also achieved reperfusion in three of five animals with high incidence of reocclusion. These results suggest that FK633 may be a more effective antithrombotic agent than aspirin due to its agonist-independent antiplatelet effects.
比较了FK633(一种糖蛋白IIb/IIIa拮抗剂)和阿司匹林的抗血小板及抗血栓形成作用。静脉注射0.32mg/kg的FK633或10mg/kg的阿司匹林在豚鼠体内可使体外胶原诱导的血小板聚集在1小时内抑制率>50%。然而,阿司匹林对ADP诱导的血小板聚集抑制作用较弱。采用三氯化铁诱导的豚鼠颈动脉血栓形成模型比较了FK633和阿司匹林的体内抗血栓形成作用。静脉注射0.32mg/kg的FK633预处理可显著预防闭塞性血栓形成,但静脉注射10mg/kg的阿司匹林则无此作用。在溶栓实验中,FK633(静脉注射0.32mg/kg)与重组组织型纤溶酶原激活剂(rt-PA,0.3mg/kg推注+1.0mg/kg/小时)联合使用,五只动物中有五只实现再灌注且无再闭塞发生。阿司匹林(静脉注射100mg/kg)与rt-PA联合使用时,五只动物中有三只实现再灌注,但再闭塞发生率较高。这些结果表明,由于FK633具有不依赖激动剂的抗血小板作用,它可能是一种比阿司匹林更有效的抗血栓形成药物。