Rebello S S, Blank H S, Lucchesi B R
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, USA.
Thromb Res. 2000 Jun 15;98(6):531-40. doi: 10.1016/s0049-3848(00)00210-3.
We examined the adjunctive benefit of recombinant nematode anticoagulant peptide (rNAP5), a factor Xa inhibitor, in a canine model of recombinant (rt)-PA-induced thrombolysis. In anesthetized dogs, a stable occlusive thrombus was formed by electrolytic injury of the vessel wall, after which the animals were administered rt-PA (1.44 mg/kg, i.v.) and rNAP5 (0.1 mg/kg, s.c.: n=13), or rt-PA plus vehicle (1-2 ml, s.c.; n=13). Hemodynamic and coagulation parameters were monitored for 360 minutes. Single subcutaneous administration of rNAP5 resulted in a prolonged and sustained increase in the activated partial thromboplastin time (>100-fold), whereas prothrombin time was unchanged. The template bleeding time was not altered significantly throughout the protocol (maximum 1.4-fold). The incidence of reperfusion was similar in the two groups with a trend toward faster reperfusion in the rNAP5 group (34+/-4 minutes) compared to the vehicle group (63+/-15 minutes; p=0.07). After reperfusion, 80% of the vessels in the vehicle group reoccluded, whereas only 14% of vessels reoccluded in the rNAP5-treated group. Times to reocclusion were 65+/-21 minutes and 221+/-28 minutes, respectively (p<0.05). Single subcutaneous administration of rNAP5 sustained the coronary artery blood flow after reperfusion, such that at the end of protocol the flow was 47% of the preocclusion value as compared to the vehicle group in which the flow was 11% (p<0.05). Cyclic flow reductions were most prominent during rt-PA-induced reperfusion and were similar in both groups. The results indicate that a single subcutaneous administration of rNAP5 provides a sustained antithrombotic effect in maintaining the coronary artery patency during rt-PA-induced thrombolysis.
我们在重组组织型纤溶酶原激活剂(rt-PA)诱导的溶栓犬模型中研究了重组线虫抗凝血肽(rNAP5,一种Xa因子抑制剂)的辅助益处。在麻醉的犬中,通过血管壁的电解损伤形成稳定的闭塞性血栓,之后给动物静脉注射rt-PA(1.44mg/kg)和皮下注射rNAP5(0.1mg/kg,n = 13),或rt-PA加赋形剂(1 - 2ml,皮下注射;n = 13)。监测血流动力学和凝血参数360分钟。单次皮下注射rNAP5导致活化部分凝血活酶时间延长并持续增加(>100倍),而凝血酶原时间未改变。在整个实验过程中模板出血时间无显著改变(最大1.4倍)。两组的再灌注发生率相似,rNAP5组的再灌注趋势比赋形剂组更快(34±4分钟),而赋形剂组为(63±15分钟;p = 0.07)。再灌注后,赋形剂组80%的血管再次闭塞,而rNAP5治疗组只有14%的血管再次闭塞。再次闭塞的时间分别为65±21分钟和221±28分钟(p<0.05)。单次皮下注射rNAP5在再灌注后维持冠状动脉血流,使得在实验结束时血流为闭塞前值的47%,而赋形剂组血流为11%(p<0.05)。rt-PA诱导的再灌注期间循环血流减少最为显著,且两组相似。结果表明,单次皮下注射rNAP5在rt-PA诱导的溶栓过程中维持冠状动脉通畅方面提供了持续的抗血栓作用。