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慢性犬模型中冠状动脉溶栓后再血栓形成的预防。I. 单克隆抗体7E3 F(ab')2片段的辅助治疗

Prevention of rethrombosis after coronary thrombolysis in a chronic canine model. I. Adjunctive therapy with monoclonal antibody 7E3 F(ab')2 fragment.

作者信息

Rote W E, Mu D X, Bates E R, Nedelman M A, Lucchesi B R

机构信息

Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48108-0626.

出版信息

J Cardiovasc Pharmacol. 1994 Feb;23(2):194-202.

PMID:7511747
Abstract

We examined the efficacy of the monoclonal antibody (MoAb) 7E3 F(ab')2 fragment, an inhibitor of the platelet glycoprotein (GP)IIb/IIIa receptor, to prevent coronary artery rethrombosis after successful thrombolysis with rt-PA. The circumflex coronary artery of anesthetized dogs was instrumented with a flow probe, an electrode, and a stenosis. After recovery from the surgical procedure, the animals were reanesthetized on post-operative day 9, and vessel wall injury was induced with current applied to the intimal surface of the circumflex coronary artery. The resulting occlusive thrombus was aged for 30 min, and recombinant tissue plasminogen activator (rt-PA) was administered. The animals were allocated to receive either placebo or a single dose of 7E3 [0.8 mg/kg intravenous (i.v.) bolus] as the sole adjunctive agent. Ex vivo platelet function and coronary artery blood flow velocity were recorded on each of 5 consecutive days. Reocclusion and mortality were reduced significantly in animals treated with 7E3 as compared with the placebo-treated group. Significant inhibition of ex vivo platelet aggregation persisted for 48 h after a single injection of 7E3. The MoAb 7E3 F(ab')2 fragment is effective as the sole adjunctive agent with rt-PA for prevention of rethrombosis. The present study is unique in that it examined the efficacy of GPIIb/IIIa inhibition in an experimental model for an extended time, demonstrating the duration of antiplatelet therapy required to prevent rethrombosis after thrombolysis.

摘要

我们研究了血小板糖蛋白(GP)IIb/IIIa受体抑制剂单克隆抗体(MoAb)7E3 F(ab')2片段预防rt-PA成功溶栓后冠状动脉再血栓形成的疗效。对麻醉犬的左旋冠状动脉安装流量探头、电极和狭窄装置。手术恢复后,在术后第9天再次麻醉动物,通过向左旋冠状动脉内膜表面施加电流诱导血管壁损伤。使形成的闭塞性血栓老化30分钟,然后给予重组组织型纤溶酶原激活剂(rt-PA)。将动物分为两组,分别接受安慰剂或单剂量7E3[0.8mg/kg静脉推注]作为唯一辅助药物。连续5天每天记录体外血小板功能和冠状动脉血流速度。与安慰剂治疗组相比,接受7E3治疗的动物再闭塞和死亡率显著降低。单次注射7E3后,体外血小板聚集受到显著抑制并持续48小时。MoAb 7E3 F(ab')2片段作为rt-PA的唯一辅助药物可有效预防再血栓形成。本研究的独特之处在于,它在一个实验模型中长时间研究了GPIIb/IIIa抑制的疗效,证明了溶栓后预防再血栓形成所需的抗血小板治疗持续时间。

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