The interactions between natural products and OATP1B1.
- Author:
Mei-zhi SHI
;
Yu LIU
;
Jia-lin BIAN
;
Meng JIN
;
Chun-shan GUI
- Publication Type:Journal Article
- MeSH:
Animals;
Biological Products;
CHO Cells;
Cricetulus;
Drug Interactions;
Fatty Acids, Monounsaturated;
pharmacology;
Flavonoids;
pharmacology;
Indoles;
pharmacology;
Inhibitory Concentration 50;
Organic Anion Transporters;
genetics;
metabolism;
Rosuvastatin Calcium;
pharmacology;
Structure-Activity Relationship
- From:
Acta Pharmaceutica Sinica
2015;50(7):848-853
- CountryChina
- Language:Chinese
-
Abstract:
Organic anion transporting polypeptide 1B1 (OATP1B1) is an important liver-specific uptake transporter, which mediates transport of numerous endogenous substances and drugs from blood into hepatocytes. To identify and investigate potential modulators of OATP1B1 from natural products, the effect of 21 frequently used natural compounds and extracts on OATP1B1-mediated fluorescein methotrexate transport was studied by using Chinese hamster ovary cells stably expressing OATP1B1 (CHO-OATP1B1) in 96-well plates. This method could be used for the screening of large compound libraries. Our studies showed that some flavonoids (e.g., quercetin, quercitrin, rutin, chrysanthemum flavonoids and mulberrin) and triterpenoids (e.g., glycyrrhetinic acid and glycyrrhizic acid) were inhibitors of OATP1B1 with IC50 values less than 16 µmol · L(-1). The IC50 value of glycyrrhetinic acid on OATP1B1 was comparable to its blood concentration in clinics, indicating an OATPlB1-mediated drug-drug interaction could occur. Structure-activity relationship analysis showed that flavonoids had much higher inhibitory activity than their glycosides. Furthermore, the type and length of saccharides had a significant effect on their activity. In addition, we used OATP1B1 substrates fluvastatin and rosuvastatin as probe drugs to investigate the substrate-dependent effect of several natural compounds on the function of OATP1B1 in vitro. Our results demonstrated that the effect of these natural products on the function of OATPlB1 was substrate-dependent. In summary, this study would be conducive to predicting and avoiding potential OATP1B1-mediated drug-drug and drug-food interactions and thus provide the experimental basis and guidance for rational drug use.
