Imura Y, Terashita Z, Nishikawa K
Life Sci. 1986 Jul 14;39(2):111-7. doi: 10.1016/0024-3205(86)90444-3.
The i.v. infusion of endotoxin (ET) (0.25 mg/kg/hr for 4 hr) induced disseminated intravascular coagulation (DIC) in rats; thrombocytopenia, prolongation of prothrombin time (PT) and partial thromboplastin time (PTT), hypofibrinogenemia and elevated levels of fibrinogen/fibrin degradation products (FDP) were observed. Platelet activating factor (PAF) (8 micrograms/kg/hr for 4 hr) also induced DIC-like changes, except in platelets. A specific PAF antagonist, CV-3988 (2 mg/kg bolus 5 min before ET + 1 or 2 mg/kg/hr for 4 hr of ET infusion) improved all the parameters that had been altered by both ET and PAF. CV-3988 (2 mg/kg bolus 2 hr after ET + 2 mg/kg/hr for 2 hr of ET infusion) also had beneficial effects on DIC. CV-3988 itself had no effects on the parameters of DIC. These results strongly suggest that PAF may play a role in the pathogenesis of DIC and CV-3988 may prove to be useful for the treatment of DIC.
静脉输注内毒素(ET)(0.25毫克/千克/小时,持续4小时)可诱导大鼠发生弥散性血管内凝血(DIC);观察到血小板减少、凝血酶原时间(PT)和部分凝血活酶时间(PTT)延长、纤维蛋白原血症降低以及纤维蛋白原/纤维蛋白降解产物(FDP)水平升高。血小板活化因子(PAF)(8微克/千克/小时,持续4小时)也可诱导类似DIC的变化,但血小板情况除外。一种特异性PAF拮抗剂CV - 3988(在ET前5分钟静脉推注2毫克/千克 + 在ET输注期间以1或2毫克/千克/小时持续4小时)改善了所有因ET和PAF而改变的参数。CV - 3988(在ET后2小时静脉推注2毫克/千克 + 在ET输注期间以2毫克/千克/小时持续2小时)对DIC也有有益作用。CV - 3988本身对DIC参数无影响。这些结果强烈表明PAF可能在DIC的发病机制中起作用,且CV - 3988可能被证明对DIC治疗有用。