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静脉注射糖蛋白IIb-IIIa受体拮抗剂7E3可使犬冠状动脉急性血栓性闭塞再灌注。

Intravenous administration of the glycoprotein IIb-IIIa receptor antagonist 7E3 induces reperfusion of an acute thrombotic occlusion of the canine coronary artery.

作者信息

Shetler T J, Bailey B D, Jakubowski J A, Jackson C V

机构信息

Cardiovascular Research Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285-0524, USA.

出版信息

Thromb Res. 1998 Apr 15;90(2):95-100. doi: 10.1016/s0049-3848(98)00070-x.

Abstract

The ability of the F(ab')2 fragment of the murine monoclonal antibody 7E3 directed against the platelet glycoprotein IIb-IIIa receptor complex, to cause reperfusion of a totally occluding coronary artery thrombus was examined alone and in combination with aspirin and heparin in a canine model of coronary artery thrombosis. A localized thrombus was produced in the left circumflex coronary artery in open-chest dogs by electrolytic injury of the endothelium. Intravenous administration of a single injection of 5.0 mg/kg aspirin and heparin (80 U/kg bolus plus 30 U/kg/hr x 2 hr) maintained vessel patency for approximately 101 +/- 15 minutes. After vessels had been completely occluded for 5 minutes (in the presence of aspirin + heparin), a single intravenous injection of saline (10 ml) or 0.8 mg/kg 7E3 was administered. Reperfusion was observed in all dogs (6 of 6) receiving 7E3; 4 of 6 dogs maintained vessel patency throughout the course of the 2 hour observation period. Activated partial thromboplastin and thrombin times were elevated 1.4 and 9 fold, respectively, in groups that received heparin. Template bleeding times were significantly elevated in the groups receiving 7E3. In the control group, 2 of 5 dogs reperfused briefly, however neither were patent at the end of the observation period. A third group of 4 dogs which did not receive the aspirin + heparin regimen was allowed to occlude and 5 minutes later received a single intravenous injection of 0.8 mg/kg 7E3. None of the 4 dogs in this group reperfused at any time during the study. There were no significant differences between groups in regards to hematological or hemodynamic measurements during the experiment. We concluded from these findings that the monoclonal antibody, 7E3 can promote the dissolution of friable coronary artery thrombi that evolve during standard anticoagulant and antiplatelet therapy.

摘要

在犬冠状动脉血栓形成模型中,单独以及联合阿司匹林和肝素,研究了针对血小板糖蛋白IIb-IIIa受体复合物的鼠单克隆抗体7E3的F(ab')2片段使完全闭塞的冠状动脉血栓再通的能力。通过对开胸犬左旋冠状动脉内皮进行电解损伤,形成局部血栓。静脉注射单次剂量5.0mg/kg阿司匹林和肝素(80U/kg推注加30U/kg/小时×2小时)可使血管通畅约101±15分钟。在血管完全闭塞5分钟后(在阿司匹林+肝素存在的情况下),静脉注射单次剂量生理盐水(10ml)或0.8mg/kg 7E3。接受7E3的所有犬(6只中的6只)均观察到再灌注;6只犬中有4只在2小时观察期内全程保持血管通畅。接受肝素的组中,活化部分凝血活酶时间和凝血酶时间分别升高了1.4倍和9倍。接受7E3的组中,模板出血时间显著延长。在对照组中,5只犬中有2只短暂再灌注,但在观察期结束时均未保持通畅。第三组4只未接受阿司匹林+肝素方案的犬允许血管闭塞,5分钟后静脉注射单次剂量0.8mg/kg 7E3。该组4只犬在研究期间任何时候均未再灌注。实验期间,各组在血液学或血流动力学测量方面无显著差异。我们从这些发现中得出结论,单克隆抗体7E3可促进在标准抗凝和抗血小板治疗过程中形成的易碎冠状动脉血栓的溶解。

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