School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, China; School of Pharmacy, Hainan Medical University, Haikou 571101, China.
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, China.
Thromb Res. 2014 Mar;133(3):501-6. doi: 10.1016/j.thromres.2013.12.025. Epub 2013 Dec 22.
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.
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.
Glycyrrhetinic acid in vitro directly inhibited FXa uncompetitivly with IC50 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.
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.
Xa 因子(FXa)在血液凝固中起着重要作用。本研究探讨了甘草次酸,一种源自中草药的小分子,以及它是否对 FXa 具有直接抑制作用,从而显示其抗凝活性。
在体外进行 FXa、纤溶酶、胰蛋白酶和凝血酶的酶活性、甘草次酸对 FXa 酶动力学和血浆凝固时间的抑制作用的实验。还使用大鼠尾出血模型和大鼠静脉淤滞模型分别评估体内尾出血时间和血栓形成。
甘草次酸在体外直接非竞争性抑制 FXa,IC50 为 32.6±1.24 μmol/L,与纤溶酶、凝血酶和胰蛋白酶相比,对 FXa 的选择性分别为 2、14 和 20 倍。血浆凝固时间呈剂量依赖性增加。当甘草次酸浓度达到 2.02mmol/L 时,凝血酶原时间增加一倍(PT2)。在体内实验中,甘草次酸灌胃给药导致大鼠静脉淤滞模型血栓重量呈剂量依赖性减少(均 P<0.05)。与对照组相比,50mg/kg 甘草次酸导致静脉血栓重量减少 34.8%。此外,200、300 和 400mg/kg 剂量的甘草次酸分别使大鼠尾出血模型的出血时间延长 1.1、1.5 和 1.9 倍,导致中度出血效应。
甘草次酸是 FXa 的直接抑制剂,口服有效,进一步研究可用于治疗血液凝固障碍。