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Xenobiotica
the fate of foreign compounds in biological systems
Volume 41, 2011 - Issue 4
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General Xenobiochemistry

Regulation of human pregnane X receptor and its target gene cytochrome P450 3A4 by Chinese herbal compounds and a molecular docking study

, , , , , , , , , , & show all
Pages 259-280 | Received 04 Oct 2010, Accepted 01 Nov 2010, Published online: 30 Nov 2010
 

Abstract

  1. The pregnane X receptor (PXR) plays a critical role in the regulation of human cytochrome P450 3A4 (CYP3A4) gene. In this study, we investigated the effect of an array of compounds isolated from Chinese herbal medicines on the activity of PXR using a luciferase reporter gene assay in transiently transfected HepG2 and Huh7 cells and on the expression of PXR and CYP3A4 in LS174T cells. Furthermore, molecular docking was performed to investigate the binding modes of herbal compounds with PXR.

  2. Praeruptorin A and C, salvianolic acid B, sodium danshensu, protocatechuic aldehyde, cryptotanshinone, emodin, morin, and tanshinone IIA significantly transactivated the CYP3A4 reporter gene construct in either HepG2 or Huh7 cells. The PXR mRNA expression in LS174T cells was significantly induced by physcion, protocatechuic aldehyde, salvianolic acid B, and sodium danshensu. However, epifriedelanol, morin, praeruptorin D, mulberroside A, tanshinone I, and tanshinone IIA significantly down-regulated the expression of PXR mRNA in LS174T cells.

  3. All the herbal compounds tested can be readily docked into the ligand-binding cavity of PXR mainly through hydrogen bond and aromatic interactions with Ser247, Gln285, His407, and Arg401.

  4. These findings suggest that herbal medicines can significantly regulate PXR and CYP3A4 and this has important implication in herb–drug interactions.

Acknowledgements

The work was supported by the National Basic Research Program of China (Grant No. 2009CB522707) from National Science and Technology Ministry, and the National Key Projects from Science and Technology Ministry of China (Grant No. 2009ZX09304-003). Mr. Ya-He Liu is a holder of RMIT Postgraduate (PhD) Scholarship. In addition, Mr. Sui-Lin Mo was supported by the National Nature Science Foundation of China (No. 30973905).

Declaration of interest

The authors report no declarations of interest.

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