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葡萄柚汁对健康志愿者中氯沙坦及其活性代谢物E3174药代动力学的影响。

Effect of grapefruit juice on the pharmacokinetics of losartan and its active metabolite E3174 in healthy volunteers.

作者信息

Zaidenstein R, Soback S, Gips M, Avni B, Dishi V, Weissgarten Y, Golik A, Scapa E

机构信息

Department of Internal Medicine A, Assaf Harofeh Medical Center, Sackler Faculty of Medicine, Tel-Aiv University, Zerifin, Israel.

出版信息

Ther Drug Monit. 2001 Aug;23(4):369-73. doi: 10.1097/00007691-200108000-00008.

Abstract

Grapefruit juice (GJ), a cytochrome P450 (CYP) 3A4 inhibitor, may affect the pharmacokinetics of drugs metabolized through CYP 3A4. Losartan, an angiotensin II antagonist, is converted into its main active metabolite E3174 by CYP 3A4 and CYP 2C9. The effect of GJ on losartan pharmacokinetics was assessed in a randomized crossover trial. Losartan was given to 9 volunteers with and without GJ. Concentrations of losartan and its E3174 metabolite were determined in serum by a high-performance liquid chromatography method (HPLC). Significant differences were observed in some of the pharmacokinetic parameters of losartan and its metabolite E3174 after losartan administration with and without co-administered GJ. The lag time (time to drug appearance in serum) of losartan increased significantly with co-administered GJ. The mean residence time (MRT) and half-life (t(1/2)) of the E3174 metabolite were significantly longer and the area under the concentration--time curve (AUC) of the E3174 metabolite was significantly smaller after concomitant GJ administration. The ratio AUC(losartan)/AUC(E3174) was significantly increased after concurrent grapefruit juice intake. The increased lag time of losartan and the increased MRT and t1/2 and decreased AUC of E3174 were considered indicative of simultaneous CYP 3A4 inhibition and P-glycoprotein activation. The significantly increased AUC(losartan)/AUC(E3174) ratio, however, indicates reduced losartan conversion to E3174 by CYP 3A4 metabolism as a result of co-administered GJ.

摘要

葡萄柚汁(GJ)是一种细胞色素P450(CYP)3A4抑制剂,可能会影响通过CYP 3A4代谢的药物的药代动力学。氯沙坦是一种血管紧张素II拮抗剂,通过CYP 3A4和CYP 2C9转化为其主要活性代谢物E3174。在一项随机交叉试验中评估了GJ对氯沙坦药代动力学的影响。给9名志愿者服用氯沙坦,有的服用时同时饮用GJ,有的则不饮用。采用高效液相色谱法(HPLC)测定血清中氯沙坦及其E3174代谢物的浓度。在服用氯沙坦时,无论是否同时服用GJ,氯沙坦及其代谢物E3174的一些药代动力学参数都观察到了显著差异。氯沙坦的滞后时间(药物在血清中出现的时间)在同时服用GJ时显著增加。同时服用GJ后,E3174代谢物的平均驻留时间(MRT)和半衰期(t(1/2))显著延长,而E3174代谢物的浓度-时间曲线下面积(AUC)显著减小。同时摄入葡萄柚汁后,AUC(氯沙坦)/AUC(E3174)的比值显著增加。氯沙坦滞后时间的增加以及E3174的MRT和t1/2增加以及AUC降低被认为表明同时存在CYP 3A4抑制和P-糖蛋白激活。然而,AUC(氯沙坦)/AUC(E3174)比值的显著增加表明,由于同时服用GJ,CYP 3A4代谢导致氯沙坦向E3174的转化减少。

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