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Effects of Cucurbitacin E, a Tetracyclic Triterpene Compound from Cucurbitaceae, on the Pharmacokinetics and Pharmacodynamics of Warfarin in Rats

机译:葫芦科四环三萜化合物葫芦素E对华法林在大鼠体内的药代动力学和药效学的影响

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This study firstly investigated the effects of cucurbitacin E (CuE), a tetracyclic triterpene compound from Cucurbitaceae, on the pharmacokinetics (PK) and pharmacodynamics (PD) of warfarin, a model CYP2C probe substrate, in the rat. In PK studies, the concentration of warfarin in blood samples was determined by HPLC-DAD, and the PK parameters were analysed using non-compartmental methods. In PD studies, the prothrombin time (PT) in blood plasma at each sample point was measured via thromboplastin reagents. CuE treatment (50, 100 and 200g/kg, i.p.) decreased warfarin clearance (28-32%), increased the area under the curve (AUC(0-); 55-62%) and prolonged plasma half-life (t(1/2); 58-72%). At the same time, the anticoagulation effect of warfarin (PTmax) was also significantly increased in the presence of CuE. These data demonstrated that CuE affected the PK and PD of warfarin, and these effects may be due to the inhibition of CYP2C activity by CuE. Hence, careful monitoring should be carried out during concomitant use of herbal products containing CuE with drugs that are metabolized by CYP2C enzymes.
机译:本研究首先研究了葫芦科的四环三萜化合物葫芦素E(CuE)对华法林(一种CYP2C探针模型)的药代动力学(PK)和药效学(PD)在大鼠中的影响。在PK研究中,通过HPLC-DAD测定血液样品中华法林的浓度,并使用非房室方法分析PK参数。在PD研究中,通过凝血活酶试剂测量每个采样点血浆中的凝血酶原时间(PT)。 CuE处理(50、100和200g / kg,ip)降低了华法林清除率(28-32%),增加了曲线下面积(AUC(0-); 55-62%)并延长了血浆半衰期(t( 1/2); 58-72%)。同时,在存在CuE的情况下,华法林(PTmax)的抗凝作用也显着增强。这些数据证明CuE影响华法林的PK和PD,并且这些作用可能是由于CuE抑制了CYP2C活性。因此,在将含CuE的草药产品与被CYP2C酶代谢的药物同时使用时,应进行仔细的监测。

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