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<datestamp>2017-12-21</datestamp>
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<title lang=en>Inhibitory effect of cadmium on estrogen signaling in zebrafish brain and protection by zinc</title>
<creator>Chouchene, Lina</creator>
<creator>Pellegrini, Elisabeth</creator>
<creator>Gueguen, Marie-Madeleine</creator>
<creator>Hinfray, Nathalie</creator>
<creator>Brion, François</creator>
<creator>Piccini, Benjamin</creator>
<creator>Kah, Olivier</creator>
<creator>Saïd, Khaled</creator>
<creator>Messaoudi, Imed</creator>
<creator>Pakdel, Farzad</creator>
<contributor>Université de Monastir (UM)</contributor>
<contributor>Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor>
<contributor>Institut National de l'Environnement Industriel et des Risques (INERIS)</contributor>
<contributor>This work was supported, in part, by grants from the Ministry of Higher Education, Scientific Research and Technology of Tunisia, the French Ministry of Ecology, Energy and Sustainable Development (PNRPE project MIXEZ 11-MRES-PNRPE-7-CVS-033) and “Rennes Metropole (France).” We are thankful for INSERM and University of Rennes 1 (France) for funding our research. The valuable assistance of the staff of the zebrafish facilities (INRA) is also greatly appreciated.</contributor>
<description>International audience</description>
<source>Journal of Applied Toxicology</source>
<identifier>hal-01274217</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01274217</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01274217/document</identifier>
<identifier>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01274217/file/Inhibitory%20effect%20of%20Cadmium%20on%20estrogen_accepted.pdf</identifier>
<source>https://hal-univ-rennes1.archives-ouvertes.fr/hal-01274217</source>
<source>Journal of Applied Toxicology, 2016, 36 (6), pp.863-871. 〈10.1002/jat.3285〉</source>
<identifier>DOI : 10.1002/jat.3285</identifier>
<relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/jat.3285</relation>
<identifier>PUBMED : 26857037</identifier>
<relation>info:eu-repo/semantics/altIdentifier/pmid/26857037</relation>
<language>en</language>
<subject lang=en>Aromatase</subject>
<subject lang=en> Cadmium</subject>
<subject lang=en> Estradiol</subject>
<subject lang=en> estrogen receptor</subject>
<subject lang=en> Zinc</subject>
<subject>[SDV.TOX.ECO] Life Sciences [q-bio]/Toxicology/Ecotoxicology</subject>
<subject>[SDE.BE] Environmental Sciences/Biodiversity and Ecology</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>The present study was conducted to assess the effects of Cd exposure on estrogen signaling in the zebrafish brain, as well as the potential protective role of Zn against Cd-induced toxicity. For this purpose, the effects on transcriptional activation of the estrogen receptors (ERs), aromatase B (Aro-B) protein expression and molecular expression of related genes were examined in vivo using wild-type and transgenic zebrafish embryos. For in vitro studies, an ER-negative glial cell line (U251MG) transfected with different zebrafish ER subtypes (ERα, ERβ1 and ERβ2) was also used. Embryos were exposed either to estradiol (E2), Cd, E2+Cd or E2+Cd+Zn for 72 h and cells were exposed to the same treatments for 30 h. Our results show that E2 treatment promoted the transcriptional activation of ERs and increased Aro-B expression, at both the protein and mRNA levels. Although exposure to Cd, does not affect the studied parameters when administered alone, it significantly abolished the E2-stimulated transcriptional response of the reporter gene for the three ER subtypes in U251-MG cells, and clearly inhibited the E2 induction of Aro-B in radial glial cells of zebrafish embryos. These inhibitory effects were accompanied by a significant downregulation of the expression of esr1, esr2a, esr2b and cyp19a1b genes compared to the E2-treated group used as a positive control. Zn administration during simultaneous exposure to E2 and Cd strongly stimulated zebrafish ERs transactivation and increased Aro-B protein expression, whereas mRNA levels of the three ERs as well as the cyp19a1b remained unchanged in comparison with Cd-treated embryos. In conclusion, our results clearly demonstrate that Cd acts as a potent anti-estrogen in vivo and in vitro, and that Cd-induced E2 antagonism can be reversed, at the protein level, by Zn supplement. </description>
<date>2016</date>
<rights>info:eu-repo/semantics/OpenAccess</rights>
</dc>
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