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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:32:53Z</responseDate> <request identifier=oai:HAL:inserm-00876125v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:inserm-00876125v1</identifier> <datestamp>2018-01-08</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdv</setSpec> <setSpec>collection:INSERM</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:IFR140</setSpec> <setSpec>collection:VALDAURELLE</setSpec> <setSpec>collection:FNCLCC</setSpec> <setSpec>collection:MARQUIS</setSpec> <setSpec>collection:HL</setSpec> <setSpec>collection:U991</setSpec> <setSpec>collection:UNIV-RENNES1</setSpec> <setSpec>collection:IRSET</setSpec> <setSpec>collection:IRSET-ERD</setSpec> <setSpec>collection:IRSET-VCER</setSpec> <setSpec>collection:BIOSIT</setSpec> <setSpec>collection:NUMECAN</setSpec> <setSpec>collection:UR1-UFR-SVE</setSpec> <setSpec>collection:STATS-UR1</setSpec> <setSpec>collection:UR1-HAL</setSpec> <setSpec>collection:EHESP</setSpec> <setSpec>collection:USPC</setSpec> <setSpec>collection:UR1-SDV</setSpec> <setSpec>collection:IRSET-8</setSpec> <setSpec>collection:IRSET-9</setSpec> <setSpec>collection:UNIV-ANGERS</setSpec> <setSpec>collection:IRSET-EHESP</setSpec> <setSpec>collection:BS</setSpec> <setSpec>collection:UNIV-MONTPELLIER</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Paracetamol, aspirin and indomethacin induce endocrine disturbances in the human fetal testis capable of interfering with testicular descent.</title> <creator>Mazaud-Guittot, Séverine</creator> <creator>Nicolaz, Christophe Nicolas</creator> <creator>Desdoits-Lethimonier, Christèle</creator> <creator>Coiffec, Isabelle</creator> <creator>Maamar, Millissia Ben</creator> <creator>Balaguer, Patrick</creator> <creator>Kristensen, David, </creator> <creator>Chevrier, Cécile</creator> <creator>Lavoué, Vincent</creator> <creator>Poulain, Patrice</creator> <creator>Dejucq-Rainsford, Nathalie</creator> <creator>Jégou, Bernard</creator> <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 de recherche en cancérologie de Montpellier (IRCM) ; Université Montpellier 1 (UM1) - CRLCC Val d'Aurelle - Paul Lamarque - Institut National de la Santé et de la Recherche Médicale (INSERM) - Université de Montpellier (UM)</contributor> <contributor>Microenvironnement et remodelage ; Foie, métabolismes et cancer ; Université de Rennes 1 (UR1) - 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 ) - Université de Rennes 1 (UR1) - 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 ) - Service de Gynécologie et Obstétrique [Rennes] ; Université de Rennes 1 (UR1) - CHU Pontchaillou [Rennes] - Hôpital Sud - CHU Pontchaillou [Rennes] - Hôpital Sud - CRLCC Eugène Marquis (CRLCC)</contributor> <contributor>Service d'obstétrique ; Service de Gynécologie et Obstétrique [Rennes] ; Université de Rennes 1 (UR1) - CHU Pontchaillou [Rennes] - Hôpital Sud - Université de Rennes 1 (UR1) - CHU Pontchaillou [Rennes] - Hôpital Sud</contributor> <contributor>INSERM, Université de Rennes1, EHESP, Agence Nationale de Sécurité du Médicament et des Produits de Santé, Danish Council for independent Research</contributor> <description>International audience</description> <source>ISSN: 0021-972X</source> <source>EISSN: 1945-7197</source> <source>Journal of Clinical Endocrinology and Metabolism</source> <publisher>Endocrine Society</publisher> <identifier>inserm-00876125</identifier> <identifier>http://www.hal.inserm.fr/inserm-00876125</identifier> <source>http://www.hal.inserm.fr/inserm-00876125</source> <source>Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2013, 98 (11), pp.E1757-67. 〈10.1210/jc.2013-2531〉</source> <identifier>DOI : 10.1210/jc.2013-2531</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1210/jc.2013-2531</relation> <identifier>PUBMED : 24030937</identifier> <relation>info:eu-repo/semantics/altIdentifier/pmid/24030937</relation> <language>en</language> <subject>[SDV.BDD] Life Sciences [q-bio]/Development Biology</subject> <subject>[SDV.SP] Life Sciences [q-bio]/Pharmaceutical sciences</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>: Context:Masculinization depends on the fetal testis. Exposure of the human fetus during pregnancy to paracetamol or/and to other mild-analgesics is associated with an increased risk of cryptorchidism.Objective:We aimed at determining whether mild analgesics disrupted the morphology and endocrine function of the human testis.Design:We used an in vitro system based on the culture of human fetal testes exposed or not to paracetamol, its metabolite AM404, aspirin, indomethacin, ketoconazole at 10(-4) M to 10(-7) M.Setting:The study was conducted at the University of Rennes I.Patients/Participants:Human fetal testes were from pregnant women following induced abortion, between 7 and 12 weeks of gestation (GW).Main Outcome Measures:Testosterone (radioimmunoassay: RIA), Anti-Müllerian Hormone (AMH; ELISA), insulin-like factor 3 (INSL3; RIA), prostaglandin D2 and E2 (PGD2 and PGE2, respectively; ELISA), were assayed in the media. Testicular cells were counted using histology and image analysis. The possible nuclear receptor-mediated activities of the analgesics were investigated using reporter cell lines expressing estrogen (ERs), androgen (AR) and peroxysome proliferator-activated γ ( PPARγ) receptors.Results:Indomethacin and aspirin stimulated testosterone production, particularly by the younger testes (8-9 GW vs 10-12 GW). Paracetamol, AM404 and ketoconazole decreased INSL3 levels. Aspirin stimulated, whereas ketoconazole inhibited AMH production. PGE2 levels were inhibited by paracetamol, and aspirin in the 7-12 GW testes, and by indomethacin but only in 7-9.86 GW old testes. The inhibitory trends seen for PGD2 were not statistically significant.Conclusions:Analgesics at concentrations relevant to human exposure cause endocrine disturbances in the fetal testis. We suggest that the fetal human testis displays slight critical age windows for sensitivity to direct exposure to aspirin, indomethacin and paracetamol. The analgesic-induced inhibition of INSL3 may be the mechanism by which analgesics increase the risk of cryptorchidism. Greater caution is required concerning consumption of analgesics during pregnancy.</description> <date>2013-09-12</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>