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RETRACTED: The Aminopyridinol Derivative BJ-1201 Protects Murine Hippocampal Cells against Glutamate-Induced Neurotoxicity via Heme Oxygenase-1 (Retracted Article. See vol 21, Art no 1463, 2016)

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dc.contributor.authorLee, Dong-Sung-
dc.contributor.authorNam, Tae-Gyu-
dc.contributor.authorJeong, Byeong-Seon-
dc.contributor.authorJeong, Gil-Saeng-
dc.date.accessioned2021-06-22T17:01:30Z-
dc.date.available2021-06-22T17:01:30Z-
dc.date.created2021-01-21-
dc.date.issued2016-05-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/14023-
dc.description.abstractGlutamate is the major excitatory neurotransmitter in the brain. It can cause neuronal cell damage in the context of oxidative stress. BJ-1201 is a derivative of the compound aminopyridinol, which is known for its antioxidant activity. In this study, we examined the effect of BJ-1201, a 6-(diphenylamino)-2,4,5-trimethylpyridin-3-ol compound, on neuroprotection in HT22 cells. Our data showed that BJ-1201 can protect HT22 cells against glutamate-induced cell cytotoxicity. In addition, BJ-1201 upregulated heme oxygenase-1 (HO-1) to levels comparable to those of the CoPP-treated group. BJ-1201 treatment induced phosphorylation of JNK, but not p38-MAPK or ERK. It also increased the signal in the reporter assay based on beta-galactosidase activity driven by the nuclear transcription factor erythroid-2 related factor 2 (Nrf2) promoter harboring antioxidant response elements (AREs) and induced the translocation of Nrf2. These results demonstrate that BJ-1201 may be a good therapeutic platform against neurodegenerative diseases induced by oxidative stress.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI AG-
dc.titleRETRACTED: The Aminopyridinol Derivative BJ-1201 Protects Murine Hippocampal Cells against Glutamate-Induced Neurotoxicity via Heme Oxygenase-1 (Retracted Article. See vol 21, Art no 1463, 2016)-
dc.typeArticle-
dc.contributor.affiliatedAuthorNam, Tae-Gyu-
dc.identifier.doi10.3390/molecules21050594-
dc.identifier.scopusid2-s2.0-84973596725-
dc.identifier.wosid000380241600058-
dc.identifier.bibliographicCitationMOLECULES, v.21, no.5, pp.1 - 11-
dc.relation.isPartOfMOLECULES-
dc.citation.titleMOLECULES-
dc.citation.volume21-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.rimsART-
dc.type.docTypeArticle; Retracted Publication-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusNEUROPROTECTIVE ACTIVITY-
dc.subject.keywordPlusTHERAPEUTIC TARGET-
dc.subject.keywordPlusNERVOUS-SYSTEM-
dc.subject.keywordPlusHT22 NEURONS-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusNEUROINFLAMMATION-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusEXCITOTOXICITY-
dc.subject.keywordAuthoraminopyridinol compound BJ-1201-
dc.subject.keywordAuthorneuroprotection-
dc.subject.keywordAuthoraminopyridinol HT22-
dc.subject.keywordAuthorheme oxygenase-1-
dc.subject.keywordAuthornuclear transcription factor erythroid-2 related factor 2-
dc.identifier.urlhttps://www.mdpi.com/1420-3049/21/5/594-
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