Lynch J J, Sitko G R, Lehman E D, Vlasuk G P
Department of Pharmacology, Merck Research Laboratories, West Point, PA, USA.
Thromb Haemost. 1995 Aug;74(2):640-5.
The antithrombotic efficacies of the coagulation factor Xa inhibitor recombinant tick anticoagulant peptide (rTAP) and heparin were compared in a canine model of left circumflex (LCX) coronary artery electrolytic lesion. Intravenous infusions of saline (controls), rTAP (50 micrograms/kg/min continuous infusion) or heparin (200 U/kg bolus followed by 2 U/kg/min continuous infusion) were started 60 min prior to the initiation of LCX coronary artery electrolytic injury (150 microA continuous anodal current). All 6/6 saline-treated control animals developed occlusive thrombi at 49.8 +/- 13.6 min after the initiation of vessel injury, and possessed a residual thrombus mass of 20.7 +/- 3.3 mg. In the rTAP treatment group, 4/6 preparations developed occlusive thrombi, but with times to thrombosis delayed significantly compared to both the saline control as well as to the heparin treatment group (202.7 +/- 28.9 min; p < 0.01 to both saline and heparin groups). The remaining 2 rTAP-treated preparations remained patent despite the continued electrical stimulation of the coronary vessel for 5 h. Residual thrombus mass in the rTAP treatment group was reduced markedly compared to the saline control group (4.4 +/- 1.0 mg; p < 0.01). Heparin infusion resulted in a modest but statistically insignificant delay in occlusive LCX coronary artery thrombosis compared to saline controls, with all 6/6 heparin-treated preparations occluding at 79.7 +/- 16.5 min after the initiation of vessel injury. Residual thrombus mass in heparin-treated animals, however, was reduced compared to saline controls (9.4 +/- 1.4 mg; p < 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)
在犬左回旋支(LCX)冠状动脉电解损伤模型中,比较了凝血因子Xa抑制剂重组蜱抗凝血肽(rTAP)和肝素的抗血栓形成效果。在开始LCX冠状动脉电解损伤(150微安连续阳极电流)前60分钟,开始静脉输注生理盐水(对照组)、rTAP(50微克/千克/分钟持续输注)或肝素(200单位/千克推注,随后2单位/千克/分钟持续输注)。所有6只接受生理盐水治疗的对照动物在血管损伤开始后49.8±13.6分钟形成闭塞性血栓,残余血栓质量为20.7±3.3毫克。在rTAP治疗组中,6份制剂中有4份形成闭塞性血栓,但与生理盐水对照组以及肝素治疗组相比,血栓形成时间显著延迟(202.7±28.9分钟;与生理盐水和肝素组相比p均<0.01)。其余2份接受rTAP治疗的制剂尽管冠状动脉持续电刺激5小时仍保持通畅。与生理盐水对照组相比,rTAP治疗组的残余血栓质量显著降低(4.4±1.0毫克;p<0.01)。与生理盐水对照组相比,肝素输注使LCX冠状动脉闭塞性血栓形成出现适度但无统计学意义的延迟,所有6只接受肝素治疗的制剂在血管损伤开始后79.7±16.5分钟发生闭塞。然而,与生理盐水对照组相比,肝素治疗动物的残余血栓质量有所降低(9.4±1.4毫克;p<0.01)。(摘要截断于250字)