Co-treatment with indole-3-carbinol and resveratrol modify porcine CYP1A and CYP3A activities and expression
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
- Keywords
- Detoxification, food–drug, gene-regulation, liver, secondary plant metabolites,
- MeSH
- Cytochrome P-450 CYP1A1 antagonists & inhibitors metabolism MeSH
- Cytochrome P-450 CYP3A genetics metabolism MeSH
- Hepatocytes drug effects MeSH
- Indoles pharmacology MeSH
- Cytochrome P-450 CYP3A Inhibitors pharmacology MeSH
- Food-Drug Interactions MeSH
- Microsomes, Liver drug effects enzymology MeSH
- Swine MeSH
- Pregnane X Receptor MeSH
- Receptors, Aryl Hydrocarbon genetics MeSH
- Gene Expression Regulation, Enzymologic drug effects MeSH
- Resveratrol MeSH
- Receptors, Steroid genetics MeSH
- Stilbenes pharmacology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cytochrome P-450 CYP1A1 MeSH
- Cytochrome P-450 CYP3A MeSH
- indole-3-carbinol MeSH Browser
- Indoles MeSH
- Cytochrome P-450 CYP3A Inhibitors MeSH
- Pregnane X Receptor MeSH
- Receptors, Aryl Hydrocarbon MeSH
- Resveratrol MeSH
- Receptors, Steroid MeSH
- Stilbenes MeSH
1. Humans and animals are commonly exposed to indole-3-carbinol (I3C) and resveratrol (RES) via food or beverages. Moreover, these compounds have been demonstrated to potentially cause food-drug interactions. However, information about their combined effects is limited. Therefore, we investigated the effects of I3C and RES, both as single compounds and in combination, on cytochrome P450 1A and 3A activity and gene expression. 2. Using porcine microsomes, we demonstrated that RES caused non-competitive inhibition of CYP1A activity and un-competitive inhibition of CYP3A activity. Compared to the effect of single compounds, co-treatment with I3C and RES increased a degree of inhibition of CYP1A activity. 3. In porcine primary hepatocytes, treatment with I3C and RES resulted in induction of CYP1A1, CYP1A2 and CYP3A29 mRNA expression. 4. In conclusion, we demonstrated that both RES and I3C could cause food-drug interactions and that the combined effect could be more potent in doing so.
Agricultural Institute of Slovenia Ljubljana Slovenia and
c Department of Food Science Aarhus University Tjele Denmark
Department of Molecular Sciences Swedish University of Agricultural Sciences Uppsala Sweden
e Faculty of Agriculture and Life Sciences University of Maribor Hoče Slovenia
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