Effect of Aflatoxin B1 on Nuclear Receptors PXR, CAR, and AhR and Their Target Cytochromes P450 mRNA Expression in Primary Cultures of Human Hepatocytes

Author:

Ayed-Boussema Imen1,Pascussi Jean-Marc23,Maurel Patrick2,Bacha Hassen1,Hassen Wafa1

Affiliation:

1. Laboratory of Research on Biologically Compatible Compounds, Monastir, Tunisia

2. Laboratory of Hepatic Physiology, INSERM U632, Campus CNRS, Montpellier, France

3. INSERM U661, Institut de Génomique Fonctionnelle, Montpellier, France

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.

Publisher

SAGE Publications

Subject

Toxicology

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