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Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence

BACKGROUND: Despite numerous studies suggesting that amphibians are highly sensitive to cumulative anthropogenic stresses, the role pollutants play in the decline of amphibian populations remains unclear. Amongst the most common aquatic contaminants, polycyclic aromatic hydrocarbons (PAHs) have been...

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Autores principales: Regnault, Christophe, Worms, Isabelle AM, Oger-Desfeux, Christine, MelodeLima, Christelle, Veyrenc, Sylvie, Bayle, Marie-Laure, Combourieu, Bruno, Bonin, Aurélie, Renaud, Julien, Raveton, Muriel, Reynaud, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141109/
https://www.ncbi.nlm.nih.gov/pubmed/25103525
http://dx.doi.org/10.1186/1471-2164-15-666
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author Regnault, Christophe
Worms, Isabelle AM
Oger-Desfeux, Christine
MelodeLima, Christelle
Veyrenc, Sylvie
Bayle, Marie-Laure
Combourieu, Bruno
Bonin, Aurélie
Renaud, Julien
Raveton, Muriel
Reynaud, Stéphane
author_facet Regnault, Christophe
Worms, Isabelle AM
Oger-Desfeux, Christine
MelodeLima, Christelle
Veyrenc, Sylvie
Bayle, Marie-Laure
Combourieu, Bruno
Bonin, Aurélie
Renaud, Julien
Raveton, Muriel
Reynaud, Stéphane
author_sort Regnault, Christophe
collection PubMed
description BACKGROUND: Despite numerous studies suggesting that amphibians are highly sensitive to cumulative anthropogenic stresses, the role pollutants play in the decline of amphibian populations remains unclear. Amongst the most common aquatic contaminants, polycyclic aromatic hydrocarbons (PAHs) have been shown to induce several adverse effects on amphibian species in the larval stages. Conversely, adults exposed to high concentrations of the ubiquitous PAH, benzo[a]pyrene (BaP), tolerate the compound thanks to their highly efficient hepatic detoxification mechanisms. Due to this apparent lack of toxic effect on adults, no studies have examined in depth the potential toxicological impact of PAH on the physiology of adult amphibian livers. This study sheds light on the hepatic responses of Xenopus tropicalis when exposed to high environmentally relevant concentrations of BaP, by combining a high throughput transcriptomic approach (mRNA deep sequencing) and a characterization of cellular and physiological modifications to the amphibian liver. RESULTS: Transcriptomic changes observed in BaP-exposed Xenopus were further characterized using a time-dependent enrichment analysis, which revealed the pollutant-dependent gene regulation of important biochemical pathways, such as cholesterol biosynthesis, insulin signaling, adipocytokines signaling, glycolysis/gluconeogenesis and MAPK signaling. These results were substantiated at the physiological level with the detection of a pronounced metabolic disorder resulting in a possible insulin resistance-like syndrome phenotype. Hepatotoxicity induced by lipid and cholesterol metabolism impairments was clearly identified in BaP-exposed individuals. CONCLUSIONS: Our data suggested that BaP may disrupt overall liver physiology, and carbohydrate and cholesterol metabolism in particular, even after short-term exposure. These results are further discussed in terms of how this deregulation of liver physiology can lead to general metabolic impairment in amphibians chronically exposed to contaminants, thereby illustrating the role xenobiotics might play in the global decline in amphibian populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-666) contains supplementary material, which is available to authorized users.
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spelling pubmed-41411092014-08-28 Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence Regnault, Christophe Worms, Isabelle AM Oger-Desfeux, Christine MelodeLima, Christelle Veyrenc, Sylvie Bayle, Marie-Laure Combourieu, Bruno Bonin, Aurélie Renaud, Julien Raveton, Muriel Reynaud, Stéphane BMC Genomics Research Article BACKGROUND: Despite numerous studies suggesting that amphibians are highly sensitive to cumulative anthropogenic stresses, the role pollutants play in the decline of amphibian populations remains unclear. Amongst the most common aquatic contaminants, polycyclic aromatic hydrocarbons (PAHs) have been shown to induce several adverse effects on amphibian species in the larval stages. Conversely, adults exposed to high concentrations of the ubiquitous PAH, benzo[a]pyrene (BaP), tolerate the compound thanks to their highly efficient hepatic detoxification mechanisms. Due to this apparent lack of toxic effect on adults, no studies have examined in depth the potential toxicological impact of PAH on the physiology of adult amphibian livers. This study sheds light on the hepatic responses of Xenopus tropicalis when exposed to high environmentally relevant concentrations of BaP, by combining a high throughput transcriptomic approach (mRNA deep sequencing) and a characterization of cellular and physiological modifications to the amphibian liver. RESULTS: Transcriptomic changes observed in BaP-exposed Xenopus were further characterized using a time-dependent enrichment analysis, which revealed the pollutant-dependent gene regulation of important biochemical pathways, such as cholesterol biosynthesis, insulin signaling, adipocytokines signaling, glycolysis/gluconeogenesis and MAPK signaling. These results were substantiated at the physiological level with the detection of a pronounced metabolic disorder resulting in a possible insulin resistance-like syndrome phenotype. Hepatotoxicity induced by lipid and cholesterol metabolism impairments was clearly identified in BaP-exposed individuals. CONCLUSIONS: Our data suggested that BaP may disrupt overall liver physiology, and carbohydrate and cholesterol metabolism in particular, even after short-term exposure. These results are further discussed in terms of how this deregulation of liver physiology can lead to general metabolic impairment in amphibians chronically exposed to contaminants, thereby illustrating the role xenobiotics might play in the global decline in amphibian populations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-666) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-08 /pmc/articles/PMC4141109/ /pubmed/25103525 http://dx.doi.org/10.1186/1471-2164-15-666 Text en © Regnault et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Regnault, Christophe
Worms, Isabelle AM
Oger-Desfeux, Christine
MelodeLima, Christelle
Veyrenc, Sylvie
Bayle, Marie-Laure
Combourieu, Bruno
Bonin, Aurélie
Renaud, Julien
Raveton, Muriel
Reynaud, Stéphane
Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title_full Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title_fullStr Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title_full_unstemmed Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title_short Impaired liver function in Xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
title_sort impaired liver function in xenopus tropicalis exposed to benzo[a]pyrene: transcriptomic and metabolic evidence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141109/
https://www.ncbi.nlm.nih.gov/pubmed/25103525
http://dx.doi.org/10.1186/1471-2164-15-666
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