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Effect of Aflatoxin B1 on Nuclear Receptors PXR, CAR, and AhR and Their Target Cytochromes P450 mRNA Expression in Primary Cultures of Human Hepatocytes
- Source :
- International Journal of Toxicology. 31:86-93
- Publication Year :
- 2011
- Publisher :
- SAGE Publications, 2011.
-
Abstract
- Aflatoxin B1 (AFB1), one of the most common mycotoxins found in human foods and animal feed, is principally hepatotoxic and hepatocarcinogenic. The aim of the present study was to explore the effect of AFB1 on messenger RNA (mRNA) expression of pregnane X receptor (PXR), constitutive androstane receptor (CAR), and aryl hydrocarbon receptor (AhR) and some of their target cytochromes using primary cultures of human hepatocytes. Our results showed that AFB1, at noncytotoxic increasing concentrations, caused a significant upregulation of cytochrome P 2B6 (CYP2B6), CYP3A5, and to a lesser extent CYP3A4 and CYP2C9. Pregnane X receptor and CAR mRNA expression increased in the 3 treated livers. Aflatoxin B1 was found also to induce an overexpression of CYP1A1 and CYP1A2 genes accompanied by an increase in AhR mRNA expression. These findings suggest that AFB1 could activate PXR, CAR, and AhR; however, further investigations are needed to confirm nuclear receptor activation by AFB1.
- Subjects :
- Male
Receptors, Steroid
medicine.medical_specialty
Aflatoxin B1
Cell Survival
Receptors, Cytoplasmic and Nuclear
Biology
Toxicology
Cytochrome P-450 Enzyme System
Downregulation and upregulation
Internal medicine
Constitutive androstane receptor
medicine
Humans
RNA, Messenger
Receptor
Cells, Cultured
Constitutive Androstane Receptor
Aged
Aged, 80 and over
Messenger RNA
Pregnane X receptor
CYP3A4
Pregnane X Receptor
Middle Aged
Aryl hydrocarbon receptor
Molecular biology
Endocrinology
Gene Expression Regulation
Receptors, Aryl Hydrocarbon
Nuclear receptor
Carcinogens
Hepatocytes
biology.protein
Female
Subjects
Details
- ISSN :
- 1092874X and 10915818
- Volume :
- 31
- Database :
- OpenAIRE
- Journal :
- International Journal of Toxicology
- Accession number :
- edsair.doi.dedup.....a476ca7ff0a8641ec87064bf84e5057b
- Full Text :
- https://doi.org/10.1177/1091581811422453