Wanwimolruk Sompon, Phopin Kamonrat, Prachayasittikul Virapong
Center for Innovation Development and Technology Transfer, Faculty of Medical Technology, Mahidol University, Thailand.
Department of Clinical Microbiology and Applied Technology, Faculty of Medical Technology, Mahidol University, Thailand.
EXCLI J. 2014 Aug 20;13:869-96. eCollection 2014.
To date, a number of significant herbal drug interactions have their origins in the alteration of cytochrome P450 (CYP) activity by various phytochemicals. Among the most noteworthy are those involving St. John's wort and drugs metabolized by human CYP3A4 enzyme. This review article is the continued work from our previous article (Part 1) published in this journal (Wanwimolruk and Prachayasittikul, 2014[ref:133]). This article extends the scope of the review to six more herbs and updates information on herbal drug interactions. These include black cohosh, ginseng, grape seed extract, green tea, kava, saw palmetto and some important Chinese medicines are also presented. Even though there have been many studies to determine the effects of herbs and herbal medicines on the activity of CYP, most of them were in vitro and in animal studies. Therefore, the studies are limited in predicting the clinical relevance of herbal drug interactions. It appeared that the majority of the herbal medicines have no clear effects on most of the CYPs examined. For example, the existing clinical trial data imply that black cohosh, ginseng and saw palmetto are unlikely to affect the pharmacokinetics of conventional drugs metabolized by human CYPs. For grape seed extract and green tea, adverse herbal drug interactions are unlikely when they are concomitantly taken with prescription drugs that are CYP substrates. Although there were few clinical studies on potential CYP-mediated interactions produced by kava, present data suggest that kava supplements have the ability to inhibit CYP1A2 and CYP2E1 significantly. Therefore, caution should be taken when patients take kava with CYP1A2 or CYP2E1 substrate drugs as it may enhance their therapeutic and adverse effects. Despite the long use of traditional Chinese herbal medicines, little is known about the potential drug interactions with these herbs. Many popularly used Chinese medicines have been shown in vitro to significantly change the activity of human CYP. However, with little confirming evidence from clinical studies, precaution should be exercised when patients are taking Chinese herbal medicines concomitantly with drugs that are CYP substrates. Currently there is sufficient evidence to indicate that herbal drug interactions can occur and may lead to serious clinical consequence. Further clinical trial research should be conducted to verify these herbal drug interactions. Education on herbal drug interactions and communication with patients on their use of herbal products is also important.
迄今为止,许多重要的草药与药物相互作用源于各种植物化学物质对细胞色素P450(CYP)活性的改变。其中最值得注意的是涉及圣约翰草和由人类CYP3A4酶代谢的药物之间的相互作用。这篇综述文章是我们之前发表在本期刊上的文章(Wanwimolruk和Prachayasittikul,2014[参考文献:133])的延续。本文将综述范围扩展到另外六种草药,并更新了草药与药物相互作用的信息。这些草药包括黑升麻、人参、葡萄籽提取物、绿茶、卡瓦胡椒、锯叶棕,同时还介绍了一些重要的中药。尽管已经有很多研究来确定草药和草药制品对CYP活性的影响,但其中大多数是体外研究和动物研究。因此,这些研究在预测草药与药物相互作用的临床相关性方面存在局限性。似乎大多数草药对所检测的大多数CYP没有明显影响。例如,现有的临床试验数据表明,黑升麻、人参和锯叶棕不太可能影响由人类CYP代谢的传统药物的药代动力学。对于葡萄籽提取物和绿茶,当它们与作为CYP底物的处方药同时服用时,不太可能发生不良的草药与药物相互作用。尽管关于卡瓦胡椒产生的潜在CYP介导的相互作用的临床研究很少,但目前的数据表明,卡瓦胡椒补充剂有能力显著抑制CYP1A2和CYP2E1。因此,当患者将卡瓦胡椒与CYP1A2或CYP2E1底物药物一起服用时应谨慎,因为这可能会增强它们的治疗效果和不良反应。尽管传统中药已经使用了很长时间,但对于这些草药潜在的药物相互作用却知之甚少。许多常用的中药在体外已被证明能显著改变人类CYP的活性。然而,由于临床研究的证实证据很少,当患者同时服用中药和作为CYP底物的药物时应谨慎。目前有足够的证据表明草药与药物相互作用可能发生,并可能导致严重的临床后果。应该进行进一步的临床试验研究来验证这些草药与药物的相互作用。关于草药与药物相互作用的教育以及就患者使用草药制品进行沟通也很重要。