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Thrombolytic and Antiplatelet Effects of a Novel Plasminogen Activator from the Venom of Gloydius Brevicaudus Viper

机译:新型Glasyius Brevicaudus毒蛇毒液中纤溶酶原激活剂的溶栓和抗血小板作用

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Aim : To investigate the thrombolytic and antiplatelet effects of a novel plasminogen activator from the venom of the Gloydius brevicaudus viper (GBV-PA) in vitro and in vivo . Methods : Thrombolytic experiments were performed in rabbit models of ear vein thrombosis and carotid artery thrombosis and in dog model of acute cerebral infarction. Inhibition of thrombus formation was evaluated in rat inferior vena cava thrombosis model and ferric chloride-induced arterial thrombosis. In vitro , we assayed the antithrombotic effect of GBV-PA on rabbit blood clots, euglobulin lysis time (ELT) of rabbit plasma, and ADP-induced platelet aggregation. Results : GBV-PA intravenous administration significantly reduced vascular recanalization times of rabbit ear veins thrombosis and thrombus weight of rabbit carotid artery thrombosis. The arterial recanalization rates were dose- and time-dependently improved after the administration of GBV-PA in canine acute cerebral infarction model. Thrombus length and weight were significantly reduced by GBV-PA both in rat inferior vena cava and ferric chloride-induced arterial thrombosis models. Thrombus formation in the blood of rabbits that were administered of GBV-PA was also inhibited. GBV-PA radically reduced plasma ELT of the rabbit's blood clots. ADP-induced platelet aggregation was inhibited by GBV-PA in a dose-dependent manner with a half-maximal inhibitory concentration of 19.9 μg/mL. Conclusion : This study demonstrates that GBV-PA is a thrombolytic and antiplatelet agent. It has significant antithrombotic effects on various in vitro and in vivo experimental models of thrombosis. The mechanisms that underline its antithrombotic effects were related to GBV-PA's capabilities of increasing fibrinolytic activity and inhibition of platelet aggregation.
机译:目的:在体外和体内研究一种新型的纤溶酶原激活物,从短臂Glo蛇毒(GBV-PA)的毒液中溶栓和抗血小板作用。方法:在兔耳静脉血栓形成和颈动脉血栓形成模型以及犬急性脑梗死模型中进行溶栓实验。在大鼠下腔静脉血栓形成模型和氯化铁诱导的动脉血栓形成模型中评估了血栓形成的抑制作用。在体外,我们测定了GBV-PA对兔血凝块,兔血浆球蛋白溶解时间(ELT)和ADP诱导的血小板聚集的抗血栓形成作用。结果:GBV-PA静脉内给药可显着减少兔耳静脉血栓形成的血管再通时间和兔颈动脉血栓形成的血栓重量。在犬急性脑梗死模型中使用GBV-PA后,动脉再通率呈剂量和时间依赖性提高。在大鼠下腔静脉和氯化铁诱发的动脉血栓形成模型中,GBV-PA均可显着减少血栓长度和重量。给予GBV-PA的兔子血液中的血栓形成也被抑制。 GBV-PA从根本上减少了兔血凝块的血浆ELT。 GBV-PA以剂量依赖性方式抑制ADP诱导的血小板凝集,最大抑制浓度为19.9μg/ mL。结论:这项研究表明GBV-PA是一种溶栓和抗血小板药物。它对各种体外和体内血栓形成实验模型具有显着的抗血栓形成作用。强调其抗血栓形成作用的机制与GBV-PA增加纤溶活性和抑制血小板聚集的能力有关。

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