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Quercetin attenuates the reduction of parvalbumin in middle cerebral artery occlusion animal model

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dc.contributor.authorPark, Dong-Ju-
dc.contributor.authorKang, Ju-Bin-
dc.contributor.authorShah, Fawad-Ali-
dc.contributor.authorKoh, Phil-Ok-
dc.date.accessioned2022-12-26T10:45:27Z-
dc.date.available2022-12-26T10:45:27Z-
dc.date.created2022-12-12-
dc.date.issued2021-02-25-
dc.identifier.issn1738-6055-
dc.identifier.urihttps://scholarworks.bwise.kr/gnu/handle/sw.gnu/4074-
dc.description.abstractBackground Calcium is a critical factor involved in modulation of essential cellular functions. Parvalbumin is a calcium buffering protein that regulates intracellular calcium concentrations. It prevents rises in calcium concentrations and inhibits apoptotic processes during ischemic injury. Quercetin exerts potent antioxidant and anti-apoptotic effects during brain ischemia. We investigated whether quercetin can regulate parvalbumin expression in cerebral ischemia and glutamate toxicity-induced neuronal cell death. Adult male rats were treated with vehicle or quercetin (10 mg/kg) 30 min prior to middle cerebral artery occlusion (MCAO) and cerebral cortical tissues were collected 24 h after MCAO. We used various techniques including Western blot, reverse transcription-PCR, and immunohistochemical staining to elucidate the changes of parvalbumin expression. Results Quercetin ameliorated MCAO-induced neurological deficits and behavioral changes. Moreover, quercetin prevented MCAO-induced a decrease in parvalbumin expression. Conclusions These findings suggest that quercetin exerts a neuroprotective effect through regulation of parvalbumin expression.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGERNATURE-
dc.subjectCENTRAL-NERVOUS-SYSTEM-
dc.subjectGENE-EXPRESSION ANALYSIS-
dc.subjectRAT-BRAIN-
dc.subjectCALCIUM-
dc.subjectISCHEMIA-
dc.subjectINJURY-
dc.subjectCELLS-
dc.subjectCA2+-
dc.subjectNEURONS-
dc.subjectSTROKE-
dc.titleQuercetin attenuates the reduction of parvalbumin in middle cerebral artery occlusion animal model-
dc.typeArticle-
dc.contributor.affiliatedAuthorKoh, Phil-Ok-
dc.identifier.doi10.1186/s42826-021-00086-0-
dc.identifier.wosid000704604400001-
dc.identifier.bibliographicCitationLABORATORY ANIMAL RESEARCH, v.37, no.1-
dc.relation.isPartOfLABORATORY ANIMAL RESEARCH-
dc.citation.titleLABORATORY ANIMAL RESEARCH-
dc.citation.volume37-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002700095-
dc.description.journalClass2-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaVeterinary Sciences-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryVeterinary Sciences-
dc.subject.keywordPlusCENTRAL-NERVOUS-SYSTEM-
dc.subject.keywordPlusGENE-EXPRESSION ANALYSIS-
dc.subject.keywordPlusRAT-BRAIN-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusISCHEMIA-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusCA2+-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordPlusSTROKE-
dc.subject.keywordAuthorCerebral ischemia-
dc.subject.keywordAuthorNeuroprotection-
dc.subject.keywordAuthorParvalbumin-
dc.subject.keywordAuthorQuercetin-
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