Liu An-Chang, Zhao Li-Xia, Yu Shu-Wen, Lou Hong-Xiang
Qilu hospital of Shandong University, Jinan 250012, China.
Jinan Central Hospital Affiliated to Shandong University, Jinan 250011, China.
Chin J Nat Med. 2015 Apr;13(4):257-63. doi: 10.1016/S1875-5364(15)30012-1.
The present study was designed to determine the effects of puerarin pre-treatment on the pharmacokinetics of the oral anticoagulant agent warfarin and the antiplatelet agent clopidogrel in rats. In the treatment group, rats was gavaged with warfarin or clopidogrel after repeated treatment with puerarin at intraperitoneal doses of 20, 60, or 200 mg·kg(-1) for 7 days, while rats in the control group were administrated only with the same dose warfarin or clopidogrel. Plasma samples were obtained at the prescribed times and analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS). The results showed that rats treated with puerarin at all the test doses of 20, 60 and 200 mg·kg(-1) were found to affect the pharmacokinetics of warfarin, but not clopidogrel, suggesting a potential herb-drug interaction between puerarin and warfarin.
本研究旨在确定葛根素预处理对大鼠口服抗凝剂华法林和抗血小板药物氯吡格雷药代动力学的影响。在治疗组中,大鼠腹腔注射剂量为20、60或200mg·kg(-1)的葛根素,重复给药7天后,再灌胃给予华法林或氯吡格雷,而对照组大鼠仅给予相同剂量的华法林或氯吡格雷。在规定时间采集血浆样本,并用液相色谱串联质谱法(LC-MS/MS)进行分析。结果表明,在所有测试剂量20、60和200mg·kg(-1)下,用葛根素处理的大鼠对华法林的药代动力学有影响,但对氯吡格雷没有影响,这表明葛根素与华法林之间可能存在药草-药物相互作用。