Suppr超能文献

与圣约翰草的药物相互作用:作用机制及临床意义

Drug interactions with St John's wort : mechanisms and clinical implications.

作者信息

Mannel Marcus

机构信息

Ad libitum Medical Services, Berlin, Germany.

出版信息

Drug Saf. 2004;27(11):773-97. doi: 10.2165/00002018-200427110-00003.

Abstract

The purpose of this paper is to review preclinical and clinical evidence relating to drug interactions with preparations of the medicinal herb St John's wort (Hypericum perforatum). A systematic literature search was carried out in three electronic databases up to June 2004. Information about case reports classified as St John's wort drug interactions was retrieved from the WHO Collaborating Centre for International Drug Monitoring and from the UK Medicines and Healthcare products Regulatory Agency in June 2003. Against the background of proven efficacy in mild to moderate depressive disorders and an excellent tolerability profile in monotherapy, there is sufficient evidence from interaction studies and case reports to suggest that St John's wort may induce the cytochrome P450 (CYP) 3A4 enzyme system and the P-glycoprotein drug transporter in a clinically relevant manner, thereby reducing efficacy of co-medications. Drugs most prominently affected and contraindicated for concomitant use with St John's wort are metabolised via both CYP3A4 and P-glycoprotein pathways, including HIV protease inhibitors, HIV non-nucleoside reverse transcriptase inhibitors (only CYP3A4), the immunosuppressants ciclosporin and tacrolimus, and the antineoplastic agents irinotecan and imatinib mesylate. Efficacy of hormonal contraceptives may be impaired as reflected by case reports of irregular bleedings and unwanted pregnancies. Drugs with a narrow therapeutic index should be monitored more closely when St John's wort is added, discontinued or the dosage is changed. The St John's wort constituent hyperforin is probably responsible for CYP3A4 induction via activation of a nuclear steroid/pregnane and xenobiotic receptor (SXR/PXR) and hypericin may be assumed to be the P-glycoprotein inducing compound, although the available evidence is less convincing. Combinations of St John's wort with serotonergic agents and other antidepressants should be restricted to prescription-only, by experienced clinicians, due to potential central pharmacodynamic interactions. In conclusion, providing certain precautions and contraindications are followed, and adequate information is given to healthcare professionals and patients, the safe and effective use of quality-tested St John's wort products can be ensured.

摘要

本文旨在综述与药用草本植物圣约翰草(贯叶连翘)制剂存在药物相互作用的临床前及临床证据。截至2004年6月,我们在三个电子数据库中进行了系统的文献检索。2003年6月,从世界卫生组织国际药品监测合作中心及英国药品和医疗产品监管局获取了归类为圣约翰草药物相互作用的病例报告信息。鉴于圣约翰草在轻至中度抑郁症中已证实的疗效以及单一疗法中出色的耐受性,相互作用研究和病例报告中有足够证据表明,圣约翰草可能以临床相关方式诱导细胞色素P450(CYP)3A4酶系统和P-糖蛋白药物转运体,从而降低联合用药的疗效。与圣约翰草同时使用时受影响最显著且禁忌的药物是通过CYP3A4和P-糖蛋白途径代谢的药物,包括HIV蛋白酶抑制剂、HIV非核苷类逆转录酶抑制剂(仅通过CYP3A4)、免疫抑制剂环孢素和他克莫司,以及抗肿瘤药物伊立替康和甲磺酸伊马替尼。病例报告显示,不规则出血和意外怀孕表明激素避孕药的疗效可能受损。当添加、停用圣约翰草或改变其剂量时,应更密切监测治疗指数较窄的药物。圣约翰草成分金丝桃素可能通过激活核类固醇/孕烷和外源性物质受体(SXR/PXR)来诱导CYP3A4,尽管现有证据不太有说服力,但金丝桃可能被认为是诱导P-糖蛋白的化合物。由于潜在的中枢药效学相互作用,圣约翰草与5-羟色胺能药物和其他抗抑郁药的联合使用应仅限于由经验丰富的临床医生开具的处方。总之,只要遵循某些预防措施和禁忌,并向医疗专业人员和患者提供充分信息,就可以确保安全有效地使用经过质量检测的圣约翰草产品。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验