Key Laboratory of Geriatric Nutrition and Health, Ministry of Education, Beijing Technology and Business University, Beijing 100048, China.
Rizhao Huawei Institute of Comprehensive Health Industries, Shandong Keepfit Biotech. Co., Ltd., Rizhao 276800, China.
Molecules. 2023 Jun 13;28(12):4740. doi: 10.3390/molecules28124740.
Organic anion transporter 3 (OAT3) is predominantly expressed in the kidney and plays a vital role in drug clearance. Consequently, co-ingestion of two OAT3 substrates may alter the pharmacokinetics of the substrate. This review summarizes drug-drug interactions (DDIs) and herbal-drug interactions (HDIs) mediated by OAT3, and inhibitors of OAT3 in natural active compounds in the past decade. This provides a valuable reference for the combined use of substrate drugs/herbs for OAT3 in clinical practice in the future and for the screening of OAT3 inhibitors to avoid harmful interactions.
有机阴离子转运体 3(OAT3)主要在肾脏中表达,在药物清除中起着至关重要的作用。因此,两种 OAT3 底物的共同摄入可能会改变底物的药代动力学。本综述总结了过去十年中 OAT3 介导的药物-药物相互作用(DDI)和草药-药物相互作用(HDI),以及天然活性化合物中 OAT3 的抑制剂。这为未来临床实践中 OAT3 底物药物/草药联合使用以及筛选 OAT3 抑制剂以避免有害相互作用提供了有价值的参考。