Literature DB >> 23160819

Dietary regulation of mouse intestinal P450 expression and drug metabolism.

Peng Zhang1, Kunzhi Jia, Cheng Fang, Xin Zhou, Xinxin Ding, Qing-Yu Zhang.   

Abstract

The study was originally designed to test the hypothesis that the compensatory increase in intestinal P450 (cytochrome P450) expression in the intestinal epithelium-specific P450 reductase (CPR) knockout (IE-Cpr-null) mice was attributable to decreased metabolism of putative P450 inducers present in the diet. Thus, we determined the impact of a dietary change from regular rodent chow to a synthetic diet devoid of phytochemicals on the expression of P450 enzymes in the small intestine (SI) and liver of wild-type (WT) and IE-Cpr-null mice. The dietary change diminished expression of CYP1A, 2B, 2C, and 3A in SI and CYP2B, 2C, and 3A in liver of both WT and IE-Cpr-null mice. However, the compensatory increase in SI P450 expression still occurred in IE-Cpr-null, compared with WT, mice, on the synthetic diet. The diet change-induced decrease in P450 expression was accompanied by decreases in microsomal midazolam-hydroxylase activity in vitro and first-pass clearance of midazolam in vivo in WT mice. Further studies showed that the dietary change, but not Cpr deletion, caused large decreases in bile acid (BA) levels in plasma, liver, SI, and intestinal content and that treatment of WT mice on the synthetic diet with GW4064, a farnesoid-X-receptor agonist, restored the levels of CYP3A expression in both liver and SI to those seen in mice fed with regular chow. Taken together, these results highlight the vital role of diet in maintaining adequate expression of major drug-metabolizing P450s and their associated drug-metabolizing activities in the digestive tract and suggest potential involvement of BA signaling in the regulatory mechanisms.

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Year:  2012        PMID: 23160819      PMCID: PMC3558856          DOI: 10.1124/dmd.112.049403

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  30 in total

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Journal:  Drug Metab Dispos       Date:  2003-12       Impact factor: 3.922

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Authors:  Camille P Granvil; Ai-Ming Yu; Guillermo Elizondo; Taro E Akiyama; Connie Cheung; Lionel Feigenbaum; Kristopher W Krausz; Frank J Gonzalez
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4.  Pregnane X receptor is a target of farnesoid X receptor.

Authors:  Diana Jung; David J Mangelsdorf; Urs A Meyer
Journal:  J Biol Chem       Date:  2006-05-08       Impact factor: 5.157

5.  Hepatic gene expression changes in mouse models with liver-specific deletion or global suppression of the NADPH-cytochrome P450 reductase gene. Mechanistic implications for the regulation of microsomal cytochrome P450 and the fatty liver phenotype.

Authors:  Yan Weng; Concetta C DiRusso; Andrew A Reilly; Paul N Black; Xinxin Ding
Journal:  J Biol Chem       Date:  2005-07-08       Impact factor: 5.157

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Journal:  Pharmacogenetics       Date:  2004-10

10.  Dietary phytochemicals regulate whole-body CYP1A1 expression through an arylhydrocarbon receptor nuclear translocator-dependent system in gut.

Authors:  Shinji Ito; Chi Chen; Junko Satoh; Sunhee Yim; Frank J Gonzalez
Journal:  J Clin Invest       Date:  2007-07       Impact factor: 14.808

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  2 in total

1.  Regulation of intestinal cytochrome P450 expression by hepatic cytochrome P450: possible involvement of fibroblast growth factor 15 and impact on systemic drug exposure.

Authors:  Yi Zhu; Xinxin Ding; Cheng Fang; Qing-Yu Zhang
Journal:  Mol Pharmacol       Date:  2013-11-01       Impact factor: 4.436

Review 2.  An update on the role of intestinal cytochrome P450 enzymes in drug disposition.

Authors:  Fang Xie; Xinxin Ding; Qing-Yu Zhang
Journal:  Acta Pharm Sin B       Date:  2016-08-04       Impact factor: 11.413

  2 in total

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