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三七或其生物活性化合物与治疗药物之间的草药-药物相互作用:全面的药效学和药代动力学综述。

Herb-drug interactions between Panax notoginseng or its biologically active compounds and therapeutic drugs: A comprehensive pharmacodynamic and pharmacokinetic review.

机构信息

Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, The MOE Key Laboratory for Standardization of Chinese Medicines, Shanghai R&D Centre for Standardization of Chinese Medicines, 1200 Cailun Road, Shanghai, 201203, China.

Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, The MOE Key Laboratory for Standardization of Chinese Medicines, Shanghai R&D Centre for Standardization of Chinese Medicines, 1200 Cailun Road, Shanghai, 201203, China.

出版信息

J Ethnopharmacol. 2023 May 10;307:116156. doi: 10.1016/j.jep.2023.116156. Epub 2023 Feb 6.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Herbs, along with the use of herb-drug interactions (HDIs) to combat diseases, are increasing in popularity worldwide. HDIs have two effects: favorable interactions that tend to improve therapeutic outcomes and/or minimize the toxic effects of drugs, and unfavorable interactions aggravating the condition of patients. Panax notoginseng (Burk.) F.H. Chen is a medicinal plant that has long been commonly used in traditional Chinese medicine to reduce swelling, relieve pain, clear blood stasis, and stop bleeding. Numerous studies have demonstrated the existence of intricate pharmacodynamic (PD) and pharmacokinetic (PK) interactions between P. notoginseng and conventional drugs. However, these HDIs have not been systematically summarized.

AIM OF THE REVIEW

To collect the available literature on the combined applications of P. notoginseng and drugs published from 2005 to 2022 and summarize the molecular mechanisms of interactions to circumvent the potential risks of combination therapy.

MATERIALS AND METHODS

This work was conducted by searching PubMed, Scopus, Web of Science, and CNKI databases. The search terms included "notoginseng", "Sanqi", "drug interaction," "synergy/synergistic", "combination/combine", "enzyme", "CYP", and "transporter".

RESULTS

P. notoginseng and its bioactive ingredients interact synergistically with numerous drugs, including anticancer, antiplatelet, and antimicrobial agents, to surmount drug resistance and side effects. This review elaborates on the molecular mechanisms of the PD processed involved. P. notoginseng shapes the PK processes of the absorption, distribution, metabolism, and excretion of other drugs by regulating metabolic enzymes and transporters, mainly cytochrome P450 enzymes and P-glycoprotein. This effect is a red flag for drugs with a narrow therapeutic window. Notably, amphipathic saponins in P. notoginseng act as auxiliary materials in drug delivery systems to enhance drug solubility and absorption and represent a new entry point for studying interactions.

CONCLUSION

This article provides a comprehensive overview of HDIs by analyzing the results of the in vivo and in vitro studies on P. notoginseng and its bioactive components. The knowledge presented here offers a scientific guideline for investigating the clinical importance of combination therapies. Physicians and patients need information on possible interactions between P. notoginseng and other drugs, and this review can help them make scientific predictions regarding the consequences of combination treatments.

摘要

民族药理学相关性

草药以及草药-药物相互作用(HDIs)在全球范围内越来越受欢迎,用于对抗疾病。HDIs 有两种作用:有利的相互作用,倾向于改善治疗效果和/或最小化药物的毒性作用,以及不利的相互作用,使患者病情恶化。三七(Panax notoginseng)(Burk.)F.H. Chen 是一种药用植物,长期以来在中国传统医学中被广泛用于消肿、止痛、活血化瘀、止血。大量研究表明,三七与常规药物之间存在复杂的药效学(PD)和药代动力学(PK)相互作用。然而,这些 HDIs 尚未得到系统总结。

综述目的

收集 2005 年至 2022 年发表的关于三七与药物联合应用的现有文献,并总结相互作用的分子机制,以规避联合治疗的潜在风险。

材料和方法

本研究通过检索 PubMed、Scopus、Web of Science 和中国知网(CNKI)数据库进行。检索词包括“notoginseng”、“Sanqi”、“drug interaction”、“synergy/synergistic”、“combination/combine”、“enzyme”、“CYP”和“transporter”。

结果

三七及其生物活性成分与多种药物(包括抗癌、抗血小板和抗菌药物)协同作用,克服药物耐药性和副作用。本综述详细阐述了所涉及的药效学处理的分子机制。三七通过调节代谢酶和转运体,主要是细胞色素 P450 酶和 P-糖蛋白,来塑造其他药物的吸收、分布、代谢和排泄的 PK 过程。这种作用是药物治疗窗狭窄的一个危险信号。值得注意的是,三七中的两亲性皂苷作为药物递送系统的辅料,可增强药物的溶解度和吸收,代表了研究相互作用的新切入点。

结论

本文通过分析三七及其生物活性成分的体内和体外研究结果,全面概述了 HDIs。本文提供的知识为研究联合治疗的临床重要性提供了科学指导。医生和患者需要了解三七与其他药物之间可能存在的相互作用的信息,本综述可以帮助他们对联合治疗的后果做出科学预测。

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