Christensen Hege, Asberg Anders, Holmboe Aase-Britt, Berg Knut Joachim
Department of Pharmacology, School of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
Eur J Clin Pharmacol. 2002 Nov;58(8):515-20. doi: 10.1007/s00228-002-0516-8. Epub 2002 Oct 16.
Grapefruit juice has been reported to increase the bioavailability of several calcium-channel antagonists, i.e. the dihydropyridines and verapamil, which are cytochrome P450 3A4 (CYP3A4) substrates. The objective of the present study was to investigate the effect of grapefruit juice on the pharmacokinetics of diltiazem and the metabolites N-demethyl-diltiazem (MA) and desacetyl-diltiazem (M1).
Ten healthy male volunteers were included in a randomised, open, crossover study, comparing the effect of a single oral dose of non-retard formulated diltiazem (120 mg) administered with 250 ml grapefruit juice or water. The study was performed on two investigation days separated by 13-38 days (median 28 days). Plasma samples were collected for measurement of diltiazem and the metabolites MA and M1. Blood pressure and heart rate were monitored throughout the study.
Grapefruit juice intake resulted in a statistically significant average individual increase in the area under the plasma diltiazem concentration-time curve (AUC(0-24)) of 20+/-25% ( P=0.02) compared with water. The average individual increase in peak plasma concentration (C(max)) of diltiazem after grapefruit juice administration was 22+/-37%, but this effect was not statistically significant ( P=0.14). The time to C(max) (t(max)) or terminal half-life was not affected by grapefruit juice. Considerable interindividual variability in the interaction was observed. There were no statistically significant differences in blood pressure and heart rate between the two treatments.
The present study demonstrated that a single intake of grapefruit juice (250 ml) caused a slight but statistically significant increase in the systemic exposure of diltiazem. Inhibition of intestinal metabolism and/or P-glycoprotein efflux transport may be responsible for this effect.
据报道,葡萄柚汁可提高几种钙通道拮抗剂(即二氢吡啶类和维拉帕米)的生物利用度,这些药物是细胞色素P450 3A4(CYP3A4)的底物。本研究的目的是探讨葡萄柚汁对地尔硫䓬及其代谢产物N-去甲基地尔硫䓬(MA)和去乙酰基地尔硫䓬(M1)药代动力学的影响。
10名健康男性志愿者参与了一项随机、开放、交叉研究,比较单次口服非缓释制剂地尔硫䓬(120 mg)并同时饮用250 ml葡萄柚汁或水的效果。研究在相隔13 - 38天(中位数28天)的两个研究日进行。采集血浆样本以测定地尔硫䓬及其代谢产物MA和M1。在整个研究过程中监测血压和心率。
与水相比,摄入葡萄柚汁导致血浆地尔硫䓬浓度-时间曲线下面积(AUC(0 - 24))平均个体增加20±25%(P = 0.02),具有统计学意义。饮用葡萄柚汁后地尔硫䓬的血浆峰浓度(C(max))平均个体增加22±37%,但该效应无统计学意义(P = 0.14)。达到C(max)的时间(t(max))或末端半衰期不受葡萄柚汁影响。观察到个体间相互作用存在相当大的变异性。两种治疗之间的血压和心率无统计学显著差异。
本研究表明,单次摄入葡萄柚汁(250 ml)会导致地尔硫䓬的全身暴露量略有增加,但具有统计学意义。肠道代谢和/或P-糖蛋白外排转运的抑制可能是造成这种效应的原因。