Abstract
Human exposure to heterocyclic aromatic amines (HAA) usually occurs through mixtures rather than individual compounds. However, the toxic effects and related mechanisms of co-exposure to HAA in humans remain unknown. We compared the effects of two of the most common HAA, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), individually or in combination, in the metabolically competent human hepatoma HepaRG cells. Various endpoints were measured including cytotoxicity, apoptosis, oxidative stress and DNA damage by the comet assay. Moreover, the effects of PhIP and/or MeIQx on mRNA expression and activities of enzymes involved in their activation and detoxification pathways were evaluated. After a 24 h treatment, PhIP and MeIQx, individually and in combination, exerted differential effects on apoptosis, oxidative stress, DNA damage and cytochrome P450 (CYP) activities. Only PhIP induced DNA damage. It was also a stronger inducer of CYP1A1 and CYP1B1 expression and activity than MeIQx. In contrast, only MeIQx exposure resulted in a significant induction of CYP1A2 activity. The combination of PhIP with MeIQx induced an oxidative stress and showed synergistic effects on apoptosis. However, PhIP-induced genotoxicity was abolished by a co-exposure with MeIQx. Such an inhibitory effect could be explained by a significant decrease in CYP1A2 activity which is responsible for
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Dumont, Julie;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Josse, Rozenn;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Lambert, Carine;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Antherieu, Sebastien;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f;
[2]
Aninat, Caroline;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Robin, Marie-Anne;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)];
Guguen-Guillouzo, Christiane;
[1]
Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)]
- Inserm U991, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)
- Agence Francaise de Securite Sanitaire des Aliments, F-35300 Fougeres (France)
Citation Formats
Dumont, Julie, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Josse, Rozenn, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Lambert, Carine, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Antherieu, Sebastien, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f, Aninat, Caroline, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Robin, Marie-Anne, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Guguen-Guillouzo, Christiane, and Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)].
Differential toxicity of heterocyclic aromatic amines and their mixture in metabolically competent HepaRG cells.
United States: N. p.,
2010.
Web.
doi:10.1016/j.taap.2010.03.008.
Dumont, Julie, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Josse, Rozenn, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Lambert, Carine, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Antherieu, Sebastien, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f, Aninat, Caroline, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Robin, Marie-Anne, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Guguen-Guillouzo, Christiane, & Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)].
Differential toxicity of heterocyclic aromatic amines and their mixture in metabolically competent HepaRG cells.
United States.
https://doi.org/10.1016/j.taap.2010.03.008
Dumont, Julie, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Josse, Rozenn, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Lambert, Carine, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Antherieu, Sebastien, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f, Aninat, Caroline, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Robin, Marie-Anne, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Guguen-Guillouzo, Christiane, and Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)].
2010.
"Differential toxicity of heterocyclic aromatic amines and their mixture in metabolically competent HepaRG cells."
United States.
https://doi.org/10.1016/j.taap.2010.03.008.
@misc{etde_21460172,
title = {Differential toxicity of heterocyclic aromatic amines and their mixture in metabolically competent HepaRG cells}
author = {Dumont, Julie, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Josse, Rozenn, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Lambert, Carine, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Antherieu, Sebastien, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f, Aninat, Caroline, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Robin, Marie-Anne, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Guguen-Guillouzo, Christiane, and Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)]}
abstractNote = {Human exposure to heterocyclic aromatic amines (HAA) usually occurs through mixtures rather than individual compounds. However, the toxic effects and related mechanisms of co-exposure to HAA in humans remain unknown. We compared the effects of two of the most common HAA, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), individually or in combination, in the metabolically competent human hepatoma HepaRG cells. Various endpoints were measured including cytotoxicity, apoptosis, oxidative stress and DNA damage by the comet assay. Moreover, the effects of PhIP and/or MeIQx on mRNA expression and activities of enzymes involved in their activation and detoxification pathways were evaluated. After a 24 h treatment, PhIP and MeIQx, individually and in combination, exerted differential effects on apoptosis, oxidative stress, DNA damage and cytochrome P450 (CYP) activities. Only PhIP induced DNA damage. It was also a stronger inducer of CYP1A1 and CYP1B1 expression and activity than MeIQx. In contrast, only MeIQx exposure resulted in a significant induction of CYP1A2 activity. The combination of PhIP with MeIQx induced an oxidative stress and showed synergistic effects on apoptosis. However, PhIP-induced genotoxicity was abolished by a co-exposure with MeIQx. Such an inhibitory effect could be explained by a significant decrease in CYP1A2 activity which is responsible for PhIP genotoxicity. Our findings highlight the need to investigate interactions between HAA when assessing risks for human health and provide new insights in the mechanisms of interaction between PhIP and MeIQx.}
doi = {10.1016/j.taap.2010.03.008}
journal = []
issue = {2}
volume = {245}
place = {United States}
year = {2010}
month = {Jun}
}
title = {Differential toxicity of heterocyclic aromatic amines and their mixture in metabolically competent HepaRG cells}
author = {Dumont, Julie, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Josse, Rozenn, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Lambert, Carine, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Antherieu, Sebastien, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Le Hegarat, Ludovic, E-mail: l.lehegarat@afssa.f, Aninat, Caroline, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Robin, Marie-Anne, Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)], Guguen-Guillouzo, Christiane, and Universite de Rennes 1, Faculte des Sciences Pharmaceutiques et Biologiques, F-35043 Rennes cedex (France)]}
abstractNote = {Human exposure to heterocyclic aromatic amines (HAA) usually occurs through mixtures rather than individual compounds. However, the toxic effects and related mechanisms of co-exposure to HAA in humans remain unknown. We compared the effects of two of the most common HAA, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), individually or in combination, in the metabolically competent human hepatoma HepaRG cells. Various endpoints were measured including cytotoxicity, apoptosis, oxidative stress and DNA damage by the comet assay. Moreover, the effects of PhIP and/or MeIQx on mRNA expression and activities of enzymes involved in their activation and detoxification pathways were evaluated. After a 24 h treatment, PhIP and MeIQx, individually and in combination, exerted differential effects on apoptosis, oxidative stress, DNA damage and cytochrome P450 (CYP) activities. Only PhIP induced DNA damage. It was also a stronger inducer of CYP1A1 and CYP1B1 expression and activity than MeIQx. In contrast, only MeIQx exposure resulted in a significant induction of CYP1A2 activity. The combination of PhIP with MeIQx induced an oxidative stress and showed synergistic effects on apoptosis. However, PhIP-induced genotoxicity was abolished by a co-exposure with MeIQx. Such an inhibitory effect could be explained by a significant decrease in CYP1A2 activity which is responsible for PhIP genotoxicity. Our findings highlight the need to investigate interactions between HAA when assessing risks for human health and provide new insights in the mechanisms of interaction between PhIP and MeIQx.}
doi = {10.1016/j.taap.2010.03.008}
journal = []
issue = {2}
volume = {245}
place = {United States}
year = {2010}
month = {Jun}
}