McWhorter School of Pharmacy, Samford University, Birmingham, AL 35229, USA.
J Pharm Pharmacol. 2013 Jul;65(7):1014-25. doi: 10.1111/jphp.12055. Epub 2013 Mar 25.
The aim of this study was to investigate the impact of commercially available, over-the-counter herbal supplements (St John's wort, black cohosh and ginger root extract) on the metabolic activation of tamoxifen and irinotecan.
Co-incubation of each drug and supplement combination over a range of concentrations was conducted in human liver microsomes and the decrease in the rate of active metabolite formation was monitored using high-performance liquid chromatography tandem mass spectrometry. Data was analysed using non-linear regression analysis and Dixon plots to determine the dominant mechanism of inhibition and to estimate the Ki and IC50 values of the commercial supplements.
The data suggest that black cohosh was the strongest inhibitor tested in this study for both CYP450 and carboxyesterase mediated biotransformation of tamoxifen and irinotecan, respectively, to their active metabolites. St John's wort was a stronger inhibitor compared with ginger root extract for tamoxifen (CYP mediated pathway), while ginger root extract was a stronger inhibitor compared with St John's wort for the carboxyesterase mediated pathway.
Commercially available supplements are widely used by patients and their potential impact on the efficacy of the chemotherapy is often unknown. The clinical significance of these results needs to be evaluated in a comprehensive clinical trial.
本研究旨在探讨市售非处方草药补充剂(圣约翰草、黑升麻和姜根提取物)对他莫昔芬和伊立替康代谢活化的影响。
在人肝微粒体中,对每种药物与补充剂组合在一系列浓度下进行共孵育,并使用高效液相色谱-串联质谱监测活性代谢物形成率的降低。使用非线性回归分析和 Dixon 图来分析数据,以确定主要的抑制机制,并估算商业补充剂的 Ki 和 IC50 值。
数据表明,黑升麻是本研究中测试的最强抑制剂,分别针对 CYP450 和羧基酯酶介导的他莫昔芬和伊立替康转化为其活性代谢物。圣约翰草对他莫昔芬(CYP 介导途径)的抑制作用强于姜根提取物,而姜根提取物对羧基酯酶介导途径的抑制作用强于圣约翰草。
市售的补充剂被广泛用于患者,但其对化疗疗效的潜在影响通常是未知的。需要在全面的临床试验中评估这些结果的临床意义。