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Induction of Per1 expression following an experimentally induced epilepsy in the mouse hippocampus

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dc.contributor.authorEun, Bokkee-
dc.contributor.authorKim, Hyun Jung-
dc.contributor.authorKim, Soo Young-
dc.contributor.authorKim, Tae Woo-
dc.contributor.authorHong, Soon Taek-
dc.contributor.authorChoi, Kyung Mi-
dc.contributor.authorShim, Jae Kwang-
dc.contributor.authorMoon, Younghye-
dc.contributor.authorSon, Gi Hoon-
dc.contributor.authorKim, Kyungjin-
dc.contributor.authorKim, Hyun-
dc.contributor.authorSun, Woong-
dc.date.accessioned2021-09-07T10:41:57Z-
dc.date.available2021-09-07T10:41:57Z-
dc.date.created2021-06-19-
dc.date.issued2011-07-08-
dc.identifier.issn0304-3940-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/112003-
dc.description.abstractThe Period1 (Per1) is a clock-oscillating gene product that plays an essential role in the generation and modulation of circadian rhythm in the suprachiasmatic nucleus (SCN) of hypothalamus. However, Per1 is also expressed in many other brain regions including cerebral cortex, hippocampus, and amygdala, suggesting that Pen l may be involved in the broader cellular functions in addition to the rhythm regulation. In this study, we found that chemical or electrical seizure-inducing stimulations regulate Pen 1 expression. Treatments with electric convulsive shock (ECS) or kainic acid (KA) robustly up-regulated the expressions of pen l mRNA and protein in the hippocampal formation and cerebral cortex. In consistent, we found that neuronal depolarization or KA treatment increased pen l mRNA expression in cultured primary cortical neurons. Because it has been demonstrated that Per family molecules contribute to the regulation of stress-induced cell death, we also explored the effect of Pen l overexpression on the survival of cultured neurons. However, neither basal, staurosporine- nor KA-induced neuronal death was affected by forced expression of Pert Collectively, these results suggest that the Pen l expression is neuronal activity- and epileptogen-dependent, although its functional significance is remained to be explored. (C) 2011 Elsevier Ireland Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectMAMMALIAN CIRCADIAN CLOCK-
dc.subjectSUPRACHIASMATIC NUCLEUS-
dc.subjectHISTONE ACETYLATION-
dc.subjectRAT-BRAIN-
dc.subjectGENE-
dc.subjectMPER1-
dc.subjectTRANSCRIPTION-
dc.subjectRHYTHMS-
dc.subjectNEURONS-
dc.subjectPERIOD-
dc.titleInduction of Per1 expression following an experimentally induced epilepsy in the mouse hippocampus-
dc.typeArticle-
dc.contributor.affiliatedAuthorSon, Gi Hoon-
dc.contributor.affiliatedAuthorKim, Hyun-
dc.contributor.affiliatedAuthorSun, Woong-
dc.identifier.doi10.1016/j.neulet.2011.03.039-
dc.identifier.scopusid2-s2.0-79958704528-
dc.identifier.wosid000292427500002-
dc.identifier.bibliographicCitationNEUROSCIENCE LETTERS, v.498, no.2, pp.110 - 113-
dc.relation.isPartOfNEUROSCIENCE LETTERS-
dc.citation.titleNEUROSCIENCE LETTERS-
dc.citation.volume498-
dc.citation.number2-
dc.citation.startPage110-
dc.citation.endPage113-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusMAMMALIAN CIRCADIAN CLOCK-
dc.subject.keywordPlusSUPRACHIASMATIC NUCLEUS-
dc.subject.keywordPlusHISTONE ACETYLATION-
dc.subject.keywordPlusRAT-BRAIN-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusMPER1-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusRHYTHMS-
dc.subject.keywordPlusNEURONS-
dc.subject.keywordPlusPERIOD-
dc.subject.keywordAuthorPer1-
dc.subject.keywordAuthorSeizure-
dc.subject.keywordAuthorHippocampus-
dc.subject.keywordAuthorKainic acid-
dc.subject.keywordAuthorElectroconvulsive shock (ECS)-
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