Steatosis and Metabolic Disorders Associated with Synergistic Activation of the CAR/RXR Heterodimer by Pesticides

Bibliographic Details
Title: Steatosis and Metabolic Disorders Associated with Synergistic Activation of the CAR/RXR Heterodimer by Pesticides
Authors: Yannick Dauwe, Lucile Mary, Fabiana Oliviero, Marina Grimaldi, Patrick Balaguer, Véronique Gayrard, Laïla Mselli-Lakhal
Source: Cells, Vol 12, Iss 8, p 1201 (2023)
Publisher Information: MDPI AG, 2023.
Publication Year: 2023
Collection: LCC:Cytology
Subject Terms: CAR, RXR, nuclear, receptor, pesticides, steatosis, Cytology, QH573-671
More Details: The nuclear receptor, constitutive androstane receptor (CAR), which forms a heterodimer with the retinoid X receptor (RXR), was initially reported as a transcription factor that regulates hepatic genes involved in detoxication and energy metabolism. Different studies have shown that CAR activation results in metabolic disorders, including non-alcoholic fatty liver disease, by activating lipogenesis in the liver. Our objective was to determine whether synergistic activations of the CAR/RXR heterodimer could occur in vivo as described in vitro by other authors, and to assess the metabolic consequences. For this purpose, six pesticides, ligands of CAR, were selected, and Tri-butyl-tin (TBT) was used as an RXR agonist. In mice, CAR’s synergic activation was induced by dieldrin associated with TBT, and combined effects were induced by propiconazole, bifenox, boscalid, and bupirimate. Moreover, a steatosis, characterized by increased triglycerides, was observed when TBT was combined with dieldrin, propiconazole, bifenox, boscalid, and bupirimate. Metabolic disruption appeared in the form of increased cholesterol and lowered free fatty acid plasma levels. An in-depth analysis revealed increased expression of genes involved in lipid synthesis and lipid import. These results contribute to the growing understanding of how environmental contaminants can influence nuclear receptor activity and associated health risks.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2073-4409
Relation: https://www.mdpi.com/2073-4409/12/8/1201; https://doaj.org/toc/2073-4409
DOI: 10.3390/cells12081201
Access URL: https://doaj.org/article/ca5c90841e094dcdaf23a68981623dfe
Accession Number: edsdoj.5c90841e094dcdaf23a68981623dfe
Database: Directory of Open Access Journals
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More Details
ISSN:20734409
DOI:10.3390/cells12081201
Published in:Cells
Language:English