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<datestamp>2015-02-21</datestamp>
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<publisher>HAL CCSD</publisher>
<title lang=en>Predicting in vivo gene expression in macrophages after exposure to benzo(a)pyrene based on in vitro assays and toxicokinetic/toxicodynamic models</title>
<creator>Péry, Alexandre R R</creator>
<creator>Brochot, Céline</creator>
<creator>Desmots, Sophie</creator>
<creator>Boize, Magali</creator>
<creator>Sparfel, Lydie</creator>
<creator>Fardel, Olivier</creator>
<contributor>Institut National de l'Environnement Industriel et des Risques (INERIS) ; INERIS</contributor>
<contributor>Service des études médicales ; EDF-GDF</contributor>
<contributor>Signalisation et Réponses aux Agents Infectieux et Chimiques (SeRAIC) ; Université de Rennes 1 (UR1) - Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; INSERM - École Nationale de la Santé Publique - Université de Rennes 1 (UR1) - Université des Antilles et de la Guyane (UAG) - Structure Fédérative de Recherche en Biologie-Santé de Rennes (Biosit) ; Université de Rennes 1 (UR1) - INSERM - CNRS - INSERM - CNRS - INSERM - École Nationale de la Santé Publique - Université de Rennes 1 (UR1) - Université des Antilles et de la Guyane (UAG) - Structure Fédérative de Recherche en Biologie-Santé de Rennes (Biosit) ; Université de Rennes 1 (UR1) - INSERM - CNRS - INSERM - CNRS - IFR140</contributor>
<contributor>French Ministry in charge of Ecology and Sustainable Development, within the framework of Programmes 189 and 190 - the European Commission 6th Framework Program, Priority 6 (Global change and ecosystems), project 2-FUN [contract #036976]</contributor>
<description>International audience</description>
<source>Toxicology Letters</source>
<publisher>Elsevier</publisher>
<identifier>hal-00873317</identifier>
<identifier>https://hal.archives-ouvertes.fr/hal-00873317</identifier>
<identifier>https://hal.archives-ouvertes.fr/hal-00873317/document</identifier>
<source>https://hal.archives-ouvertes.fr/hal-00873317</source>
<source>Toxicology Letters, Elsevier, 2011, 201 (1), pp.8-14. <10.1016/j.toxlet.2010.11.017></source>
<identifier>DOI : 10.1016/j.toxlet.2010.11.017</identifier>
<identifier>PUBMED : 21134426</identifier>
<language>en</language>
<subject lang=it>PBPK</subject>
<subject lang=it>Model calibration</subject>
<subject lang=it>BaP</subject>
<subject lang=it>Gene expression</subject>
<subject lang=it>Vitro-vivo extrapolation</subject>
<subject>[SDV.TOX] Life Sciences/Toxicology</subject>
<type>Journal articles</type>
<description lang=en>Predictive toxicology aims at developing methodologies to relate the results obtained from in vitro experiments to in vivo exposure. In the case of polycyclic aromatic hydrocarbons (PAHs), a substantial amount of knowledge on effects and modes of action has been recently obtained from in vitro studies of gene expression. In the current study, we built a physiologically based toxicokinetic (PBTK) model to relate in vivo and in vitro gene expression in case of exposure to benzo(a)pyrene (BaP), a referent PAH. This model was calibrated with two toxicokinetic datasets obtained on rats exposed either through intratracheal instillation or through intravenous administration and on an in vitro degradation study. A good agreement was obtained between the model's predictions and the concentrations measured in target organs, such as liver and lungs. Our model was able to relate correctly the gene expression for two genes targeted by PAHs, measured in vitro on primary human macrophages and in vivo in rat macrophages after exposure to BaP. Combining in vitro studies and PBTK modeling is promising for PAH risk assessment, especially for mixtures which are more efficiently studied in vitro than in vivo.</description>
<date>2011-02-25</date>
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