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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1038/s41598-020-70213-9</dc:identifier><dc:language>eng</dc:language><dc:creator>López-Granero, Caridad</dc:creator><dc:creator>Ferrer, Beatriz</dc:creator><dc:creator>Antunes dos Santos, Alessandra</dc:creator><dc:creator>Barrasa, Ángel</dc:creator><dc:creator>Ascher, Michael</dc:creator><dc:title>The BXD21/TyJ recombinant inbred strain as a model for innate inflammatory response in distinct brain regions</dc:title><dc:identifier>ART-2020-118778</dc:identifier><dc:description>Oxidative stress and inflammatory cytokines affect the human brain, increasing the risk for mood and cognitive disorders. Such risk might be selective to brain-specific regions. Here, we determined whether BXD recombinant inbred (RI) mice strains are more suitable than C57BL/6J mice for the understanding of the relationship between antioxidant response and inflammatory responses. We hypothesized that inflammatory responses could be independent of antioxidant response and be inherent to brain-specific regions. This hypothesis will be addressed by the analyses of mRNA expression. We explored, at 7-months-of-age, the innate activation of proinflammatory cytokines (tumor necrosis factor alpha (TNFα) and interleukin 6 (IL-6), as well as Kelch-like ECH-associating protein 1 (Keap1), nuclear factor erythroid 2 related factor 2 (Nrf2) and glutathione peroxidase 1 (Gpx1) mRNA in both male and female BXD84/RwwJ RI, BXD21/TyJ RI and control strain (C57BL/6J mice). We report that: (1) The cerebellum is more sensitive to antioxidant response in the BXD21/TyJ RI strain; (2) The cerebellum, hippocampus and striatum show increased levels of cytokines in the BXD21/TyJ RI strain; (3) The BXD RI strain has lower brain weight relative to control strain (C57BL/6 mice). In conclusion, our novel data show the utility of the BXD21/TyJ RI strain mice in offering mechanistic insight into Nrf2’s role in the inflammatory system.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/95063</dc:source><dc:doi>10.1038/s41598-020-70213-9</dc:doi><dc:identifier>http://zaguan.unizar.es/record/95063</dc:identifier><dc:identifier>oai:zaguan.unizar.es:95063</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/S24-17R</dc:relation><dc:identifier.citation>Scientific Reports 10 (2020), 13168 [9 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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