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转运体介导的天然产物-药物相互作用。

Transporter-mediated Natural Product-Drug Interactions.

作者信息

Bi Yajuan, Wang Xue, Ding Hui, He Feng, Han Lifeng, Zhang Youcai

机构信息

School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, P. R. China.

Department of Nutritional Sciences and Toxicology, University of California Berkeley, Berkeley, USA.

出版信息

Planta Med. 2023 Feb;89(2):119-133. doi: 10.1055/a-1803-1744. Epub 2022 Mar 18.

Abstract

The increasing use of natural products in clinical practice has raised great concerns about the potential natural product-drug interactions (NDIs). Drug transporters mediate the transmembrane passage of a broad range of drugs, and thus are important determinants for drug pharmacokinetics and pharmacodynamics. Generally, transporters can be divided into ATP binding cassette (ABC) family and solute carrier (SLC) family. Numerous natural products have been identified as inhibitors, substrates, inducers, and/or activators of drug transporters. This review article aims to provide a comprehensive summary of the recent progress on the research of NDIs, focusing on the main drug transporters, such as P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), organic anion transporter 1 and 3 (OAT1/OAT3), organic anion-transporting polypeptide 1B1 and 1B3 (OATP1B1/OATP1B3), organic cation transporter 2 (OCT2), multidrug and toxin extrusion protein 1 and 2-K (MATE1/MATE2-K). Additionally, the challenges and strategies of studying NDIs are also discussed.

摘要

天然产物在临床实践中的使用日益增加,引发了人们对潜在的天然产物-药物相互作用(NDIs)的极大关注。药物转运体介导多种药物的跨膜转运,因此是药物药代动力学和药效学的重要决定因素。一般来说,转运体可分为ATP结合盒(ABC)家族和溶质载体(SLC)家族。许多天然产物已被鉴定为药物转运体的抑制剂、底物、诱导剂和/或激活剂。这篇综述文章旨在全面总结NDIs研究的最新进展,重点关注主要的药物转运体,如P-糖蛋白(P-gp)、乳腺癌耐药蛋白(BCRP)、有机阴离子转运体1和3(OAT1/OAT3)、有机阴离子转运多肽1B1和1B3(OATP1B1/OATP1B3)、有机阳离子转运体2(OCT2)、多药和毒素外排蛋白1和2-K(MATE1/MATE2-K)。此外,还讨论了研究NDIs的挑战和策略。

相似文献

1
Transporter-mediated Natural Product-Drug Interactions.转运体介导的天然产物-药物相互作用。
Planta Med. 2023 Feb;89(2):119-133. doi: 10.1055/a-1803-1744. Epub 2022 Mar 18.

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