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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Discovery of glycyrrhetinic acid as an orally active, direct inhibitor of blood coagulation factor xa
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Discovery of glycyrrhetinic acid as an orally active, direct inhibitor of blood coagulation factor xa

机译:发现甘草次酸是一种口服活性的凝血因子xa的直接抑制剂

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摘要

Introduction Factor Xa (FXa) plays an important role in blood coagulation. This study investigated glycyrrhetinic acid, a small molecule derived from Chinese herbs, and whether it has a direct inhibitory effect on FXa to display its anticoagulant activity. Materials and Methods Enzyme activities of FXa, plasmin, trypsin and thrombin, inhibition of FXa enzyme kinetics and plasma clotting time by glycyrrhentinic acid were performed in vitro. A rat tail-bleeding model and a rat venous stasis model were also used to evaluate in vivo tail-bleeding time and thrombus formation, respectively. Results Glycyrrhetinic acid in vitro directly inhibited FXa uncompetitivly with IC 50 of 32.6 ± 1.24 μmol/L, and displayed 2-, 14- and 20-fold selectivity for FXa when compared to plasmin, thrombin and trypsin, respectively. The plasma clotting time was increased in a dose-dependent manner. The prothrombin time doubled (PT2), when the concentration of glycyrrhetinic acid reached 2.02 mmol/L. During in vivo experiments intragastric administration of glycyrrhetinic acid caused a dose-dependent reduction in thrombus weight on the rat venous stasis model (all P 0.05). 50 mg/kg glycyrrhetinic acid resulted in 34.8% of venous thrombus weight lost, compared to the control. In addition, 200, 300 and 400 mg/kg doses of glycyrrhetinic acid caused a moderate hemorrhagic effect in the rat tail-bleeding model by prolonging bleeding time 1.1-, 1.5- and 1.9-fold compared to the control, respectively. Conclusions Glycyrrhetinic acid is a direct inhibitor of FXa that is effective by oral administration, and with further research could be used to treat blood coagulation disorders.
机译:简介因子Xa(FXa)在凝血中起着重要作用。这项研究调查了甘草次酸(一种源自中草药的小分子)及其对FXa是否具有直接抑制作用以显示其抗凝活性。材料和方法在体外进行了甘草次酸的FXa,纤溶酶,胰蛋白酶和凝血酶的酶活性,FXa酶动力学的抑制以及血浆凝结时间的测定。还使用大鼠尾巴出血模型和大鼠静脉淤积模型来分别评估体内尾巴出血时间和血栓形成。结果甘草次酸在体外无竞争性地直接抑制FXa,IC 50为32.6±1.24μmol/ L,与纤溶酶,凝血酶和胰蛋白酶相比,对FXa的选择性分别高2倍,14倍和20倍。血浆凝固时间以剂量依赖性方式增加。当甘草次酸的浓度达到2.02 mmol / L时,凝血酶原时间翻倍(PT2)。在体内实验中,胃内注射甘草次酸导致大鼠静脉淤积模型的血栓重量呈剂量依赖性降低(所有P <0.05)。与对照组相比,50 mg / kg甘草次酸导致静脉血栓重量减少34.8%。此外,与对照组相比,200、300和400 mg / kg剂量的甘草次酸在大鼠尾巴出血模型中引起中度出血效应,分别延长出血时间1.1倍,1.5倍和1.9倍。结论甘草次酸是FXa的直接抑制剂,可口服有效,并且有进一步的研究可用于治疗凝血功能障碍。

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