Please use this identifier to cite or link to this item:
|Title: ||Bioavailability of the diterpenoid14-deoxy-11,12-didehydroandrographolide in rats and up-regulationof hepatic drug-metabolizing enzyme and drug transporter expression|
|Authors: ||Chih-Ching, Y;Yen, Chih-Ching;Liu, Yun-Ta;Liu, Yun-Ta;Li, Ying-Jyan;Lin, Ying-Jyan;楊雅甄;Yang, Ya-Chen;Chien-Chih, Chien-Chih C;Chen, Chien-Chih;Hsien-Tsung;Yao, Hsien-Tsung;Chen, Haw-Wen;Chen, Haw-Wen;李宗貴;Lii, Chong-Kuei|
|Issue Date: ||2019-09-02 14:09:02 (UTC+8)|
14-Deoxy-11,12-didehydroandrographolide (deAND) is the second most abundant diterpenoid in Andrographis paniculata (Burm. f.) Nees, a traditional medicine used in Asia. To date, the biological activity of deAND has not been clearly investigated.
In this study, we intended to examine the modulatory effect of deAND on hepatic drug metabolism as well as its bioavailability.
deAND prepared from A. paniculata was orally given to Sprague-Dawley rats and changes in plasma deNAD were determined by HPLC-MS. Modulation of deAND on drug-metabolizing enzyme and drug transporter expression as well as the possible mechanism involved was examined in primary rat hepatocytes.
After a single oral administration of 50 mg/kg deAND to rats, the maximum plasma concentration (Cmax), time to reach the Cmax, area under the curve (AUC0–24h), mean retention time, and half-life (t1/2) of deAND were 2.65 ± 0.68 μg/ml, 0.29 ± 0.15 h, 6.30 ± 1.66 μg/ml•h, 5.55 ± 2.52 h, and 3.56 ± 1.05 h, respectively. The oral bioavailability was 3.42%. In primary rat hepatocytes treated with up to 10 μM deAND, a dose-dependent increase was noted in the expression of cytochrome P450 (CYP) 1A1/2, CYP2C6, and CYP3A1/2; UDP-glucuronosyltransferase (UGT) 1A1, NAD(P)H:quinone oxidoreductase (NQO1), π form of GSH S-transferase (GSTP), multidrug resistance-associated protein 2, p-glycoprotein, and organic anion transporter protein 2B1. Immunoblotting assay and EMSA revealed that deAND increases the nuclear translocation and DNA binding activity of aryl hydrocarbon receptor (AhR), pregnane X receptor (PXR), and nuclear factor erythroid-derived 2-related factor 2 (Nrf2). Knockdown of AhR and Nrf2 expression abolished deAND induction of CYP isozymes and UGT1A1, NQO1, and GSTP expression, respectively.
These results indicate that deAND quickly passes through enterocytes in rats and effectively up-regulates hepatic drug-metabolizing enzyme and drug transporter expression in an AhR-, PXR-, and Nrf2-dependent manner.
|Appears in Collections:||[食品營養與保健生技學系] 期刊論文|
Files in This Item:
All items in ASIAIR are protected by copyright, with all rights reserved.