Screening and verifying potential NTCP inhibitors from herbal medicinal ingredients using the LLC-PK1 cell model stably expressing human NTCP.
10.1016/S1875-5364(16)30065-6
- Author:
Zhuo-Wei SHEN
1
;
Meng-Yue LUO
1
;
Hai-Hong HU
1
;
Hui ZHOU
1
;
Hui-Di JIANG
1
;
Lu-Shan YU
1
;
Su ZENG
2
Author Information
1. Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
2. Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China. Electronic address: zengsu@zju.edu.cn.
- Publication Type:Journal Article
- Keywords:
Biliary excretion;
Herbal medicinal ingredients;
Human NTCP;
Inhibitor;
Transport
- MeSH:
Animals;
Drug Evaluation, Preclinical;
Humans;
Kinetics;
LLC-PK1 Cells;
Models, Biological;
Organic Anion Transporters, Sodium-Dependent;
antagonists & inhibitors;
chemistry;
metabolism;
Plant Extracts;
chemistry;
pharmacology;
Plants, Medicinal;
chemistry;
Structure-Activity Relationship;
Swine;
Symporters;
antagonists & inhibitors;
chemistry;
metabolism
- From:
Chinese Journal of Natural Medicines (English Ed.)
2016;14(7):549-560
- CountryChina
- Language:English
-
Abstract:
NTCP is specifically expressed on the basolateral membrane of hepatocytes, participating in the enterohepatic circulation of bile salts, especially conjugated bile salts, to maintain bile salts homeostasis. In addition, recent studies have found that NTCP is a functional receptor of HBV and HDV. Therefore, it is important to study the interaction between drugs and NTCP and identify the inhibitors/substrates of NTCP. In the present study, a LLC-PK1 cell model stably expressing human NTCP was established, which was simple and suitable for high throughput screening, and utilized to screen and verify the potential inhibitors of NTCP from 102 herbal medicinal ingredients. The results showed that ginkgolic acid (GA) (13 : 0), GA (15 : 1), GA (17 : 1), erythrosine B, silibinin, and emodin have inhibitory effects on NTCP uptake of TCNa in a concentration-dependent manner. Among them, GA (13 : 0) and GA (15 : 1) exhibited the stronger inhibitory effects, with IC50 values being less than 8.3 and 13.5 μmol·L(-1), respectively, than the classical inhibitor, cyclosporin A (CsA) (IC50 = 20.33 μmol·L(-1)). Further research demonstrated that GA (13 : 0), GA (15 : 1), GA (17 : 1), silibinin, and emodin were not substrates of NTCP. These findings might contribute to a better understanding of the disposition of the herbal ingredients in vivo, especially in biliary excretion.
