Shebuski R J, Storer B L, Fujita T
Dept. of Pharmacology, Smith Kline & French Laboratories, King of Prussia, PA 19406.
Thromb Res. 1988 Dec 1;52(5):381-92. doi: 10.1016/0049-3848(88)90022-9.
The thrombolytic efficacy of recombinant tissue-type plasminogen activator (tPA) in the presence and absence of a thromboxane synthase inhibitor was studied in a model of femoral artery thrombosis in the anesthetized rabbit. The thrombus was formed by injection of thrombin and whole blood into an isolated segment of the femoral artery. After 30 min of stable thrombotic occlusion of the femoral artery, sodium heparin (300 U/kg, i.v.) was administered and tPA was infused locally to the site of the thrombus for 30 min at 0.01, 0.10 or 1.0 microgram/kg/min. In other experiments, CGS 13080, a selective thromboxane synthase inhibitor, was administered at a dose of 2 mg/kg i.v., 5 min before tPA was infused and at the end of the 30 min tPA infusion. Pretreatment with CGS 13080 resulted in a shorter time to tPA-induced reperfusion, greater incidence of reperfusion and increased the magnitude of femoral artery blood flow achieved after effective thrombolysis. Furthermore, pretreatment with CGS 13080 resulted in a greater than 10-fold enhancement in the effective dose of tPA. These data indicate that thromboxane synthase inhibition may be beneficial as an adjunct to thrombolytic therapy with tPA.
在麻醉兔股动脉血栓形成模型中,研究了重组组织型纤溶酶原激活剂(tPA)在存在和不存在血栓素合酶抑制剂的情况下的溶栓效果。通过将凝血酶和全血注入股动脉的分离段来形成血栓。在股动脉稳定血栓闭塞30分钟后,静脉注射肝素钠(300 U/kg),并以0.01、0.10或1.0微克/千克/分钟的速度将tPA局部注入血栓部位30分钟。在其他实验中,在注入tPA前5分钟及tPA注入30分钟结束时,静脉注射选择性血栓素合酶抑制剂CGS 13080,剂量为2毫克/千克。用CGS 13080预处理可缩短tPA诱导再灌注的时间,增加再灌注发生率,并增加有效溶栓后股动脉血流的幅度。此外,用CGS 13080预处理可使tPA的有效剂量提高10倍以上。这些数据表明,抑制血栓素合酶作为tPA溶栓治疗的辅助手段可能是有益的。