首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Antithrombotic effect of Glycyrrhizin, a plant-derived thrombin inhibitor.
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Antithrombotic effect of Glycyrrhizin, a plant-derived thrombin inhibitor.

机译:甘草甜素(一种植物凝血酶抑制剂)的抗血栓形成作用。

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摘要

Glycyrrhizin (GL), an anti-inflammatory compound isolated from licorice (Glycyrrhiza glabra), has been previously identified as a thrombin inhibitor (Francischetti et al., Biochem Biophys Res Commun 1997;235:259-63). Here we report the in vivo effects of GL upon two experimental models of induced thrombosis in rats. Intravenous administration of GL caused a dose-dependent reduction in thrombus size on a venous thrombosis model that combines stasis and hypercoagulability. It was observed that GL doses of 180 mg/kg body weight produced 93% decrease on thrombus weight. This effect showed a time-dependent pattern being significantly reduced when the thrombogenic stimulus was applied 60 min after drug administration. GL was also able to prevent thrombosis using an arteriovenous shunt model. GL doses of 180 and 360 mg/kg decreased the thrombus weight by 35 and 90%, respectively. Accordingly, the APTT ex vivo was enhanced by 1.5- and 4.3-fold at GL doses of 180 and 360 mg/kg, respectively. In addition, GL doses above 90 mg/kg caused significant hemorrhagic effect. In contrast with heparin, GL did not potentiate the inhibitory activity of antithrombin III or heparin cofactor II towards thrombin. Altogether, data indicate that GL is an effective thrombin inhibitor in vivo, which may account for its other known pharmacological properties.
机译:从甘草(甘草)分离的抗炎化合物甘草甜素(GL)先前已被鉴定为凝血酶抑制剂(Francischetti等,Biochem Biophys Res Commun 1997; 235:259-63)。在这里,我们报告GL对大鼠诱发血栓形成的两个实验模型的体内影响。在静脉血栓形成模型中,静脉内施用GL导致血栓大小呈剂量依赖性降低,该模型结合了瘀滞和高凝性。观察到180 mg / kg体重的GL剂量血栓重量减少了93%。这种作用表明,在给药60分钟后施加血栓形成刺激时,时间依赖性模式显着降低。 GL还能够使用动静脉分流模型预防血栓形成。 180和360 mg / kg的GL剂量分别使血栓重量减少了35%和90%。因此,在180和360mg / kg的GL剂量下,离体的APTT分别提高了1.5和4.3倍。此外,GL剂量超过90 mg / kg会引起明显的出血作用。与肝素相反,GL没有增强抗凝血酶III或肝素辅因子II对凝血酶的抑制活性。总而言之,数据表明GL是体内有效的凝血酶抑制剂,这可以解释其其他已知的药理特性。

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