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j.brainres.2018.09.031.pdf1.41 MBAdobe PDF見る/開く
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dc.contributor.authorAndoh, Chihiroen
dc.contributor.authorNishitani, Naoyaen
dc.contributor.authorHashimoto, Eminaen
dc.contributor.authorNagai, Yumaen
dc.contributor.authorTakao, Keizoen
dc.contributor.authorMiyakawa, Tsuyoshien
dc.contributor.authorNakagawa, Takayukien
dc.contributor.authorMori, Yasuoen
dc.contributor.authorNagayasu, Kazukien
dc.contributor.authorShirakawa, Hisashien
dc.contributor.authorKaneko, Shujien
dc.contributor.alternative安藤 千紘ja
dc.contributor.alternative西谷 直也ja
dc.contributor.alternative中川, 貴之ja
dc.contributor.alternative森, 泰生ja
dc.contributor.alternative永安, 一樹ja
dc.contributor.alternative白川, 久志ja
dc.contributor.alternative金子, 周司ja
dc.date.accessioned2019-05-27T05:38:52Z-
dc.date.available2019-05-27T05:38:52Z-
dc.date.issued2019-02-01-
dc.identifier.issn0006-8993-
dc.identifier.issn1872-6240-
dc.identifier.urihttp://hdl.handle.net/2433/241623-
dc.description.abstractTransient receptor potential melastatin 2 (TRPM2) is a Ca²⁺-permeable, nonselective cation channel and a member of the TRP channel superfamily that acts as a sensor of intracellular redox states. TRPM2 is widely distributed in many tissues and highly expressed in the brain, but the physiological roles of TRPM2 in the central nervous system remain unclear. In this study, TRPM2-deficient mice were examined in a series of behavioral tests. TRPM2-deficient mice did not significantly differ from wild-type littermates in muscle strength, light/dark transition test, rotarod, elevated plus maze, social interaction, prepulse inhibition, Y-maze, forced swim test, cued and contextual fear conditioning, and tail suspension test. In the Barnes circular maze, TRPM2-deficient mice learned the fixed escape box position at similar extent to wild-type littermates, suggesting normal reference memory. However, performance of the first reversal trial and probe test were significantly impaired in TRPM2-deficient mice. In the T-maze delayed alternation task, TRPM2 deficiency significantly reduced choice accuracy. These results indicate that TRPM2-deficient mice shows behavioral inflexibility. Meanwhile, social avoidance induced by repeated social defeat stress was significantly attenuated in TRPM2-deficient mice, suggesting that TRPM2 deficiency confers stress resiliency. Our findings indicate that TRPM2 plays an essential role in maintaining behavioral flexibility but it increases susceptibility to stress.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.en
dc.rightsThe full-text file will be made open to the public on 1 February 2020 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectTRPM2en
dc.subjectStress resiliencyen
dc.subjectBehavioral inflexibilityen
dc.titleTRPM2 confers susceptibility to social stress but is essential for behavioral flexibilityen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA10859384-
dc.identifier.jtitleBrain Research Reviewsen
dc.identifier.volume1704-
dc.identifier.spage68-
dc.identifier.epage77-
dc.relation.doi10.1016/j.brainres.2018.09.031-
dc.textversionauthor-
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki・Life Science Research Center, University of Toyamaen
dc.addressCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki・Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health Universityen
dc.addressDepartment of Clinical Pharmacology and Therapeutics, Kyoto University Hospitalen
dc.addressDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.identifier.pmid30273551-
dcterms.accessRightsopen access-
datacite.date.available2020-02-01-
datacite.awardNumber16K15125-
datacite.awardNumber17K19486-
datacite.awardNumber17H04008-
datacite.awardNumber16H05091-
dc.identifier.pissn0165-0173-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
出現コレクション:学術雑誌掲載論文等

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