Increased Systemic Exposure of Methotrexate by a Polyphenol-Rich Herb via Modulation on Efflux Transporters Multidrug Resistance-Associated Protein 2 and Breast Cancer Resistance Protein

被引:28
作者
Yu, Chung-Ping [1 ]
Hsieh, Yun-Chung [2 ]
Shia, Chi-Sheng [1 ]
Hsu, Pei-Wen [1 ]
Chen, Jen-Yuan [3 ]
Hou, Yu-Chi [1 ,2 ]
Hsieh, Yo-Wen [1 ,2 ]
机构
[1] China Med Univ, Sch Pharm, Taichung 404, Taiwan
[2] China Med Univ Hosp, Dept Pharm, Taichung 404, Taiwan
[3] China Med Univ, Grad Inst Pharmaceut Chem, Taichung 404, Taiwan
关键词
methotrexate; scutellariae radix; herb-drug interaction; MRP2; BCRP; SCUTELLARIA-BAICALENSIS; INTESTINAL-ABSORPTION; RHEUMATOID-ARTHRITIS; FOLATE TRANSPORTERS; DRUG TRANSPORTERS; CACO-2; CELLS; IN-VITRO; DISPOSITION; PHARMACOKINETICS; CHEMOTHERAPY;
D O I
10.1016/j.xphs.2015.11.031
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Scutellariae radix (SR, roots of Scutellaria baicalensis Georgi), a popular Chinese medicine, contains plenty of flavonoids such as baicalin, wogonoside, baicalein, and wogonin. Methotrexate (MTX), an important immunosuppressant with a narrow therapeutic index, is a substrate of multidrug resistance-associated proteins (MRPs) and breast cancer resistance protein (BCRP). This study investigated the effect of SR on MTX pharmacokinetics and the underlying mechanisms. Rats were orally administered MTX alone and with 1.0 or 2.0 g/kg of SR. The serum concentrations of MTX were determined by a fluorescence polarization immunoassay. Cell models were used to explore the involvement of MRP2 and BCRP in the interaction. The results showed that 1.0 g/kg of SR significantly increased C-max, AUC(0-30), AUC(0-2880), and mean residence time (MRT) of MTX by 50%, 45%, 501%, and 347%, respectively, and 2.0 g/kg of SR significantly enhanced the AUC(0-2880) and MRT by 242% and 293%, respectively, but decreased AUC0-30 by 41%. Cell line studies indicated that SR activated the BCRP-mediated efflux transport, whereas the serum metabolites of SR inhibited both the BCRP-and MRP2-mediated efflux transports. In conclusion, SR ingestion increased the systemic exposure and MRT of MTX via modulation on MRP2 and BCRP. (C) 2016 American Pharmacists Association(R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:343 / 349
页数:7
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