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Neuronal damage and gliosis in the somatosensory cortex induced by various durations of transient cerebral ischemia in gerbils

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dc.contributor.authorLee, Jae-Chul-
dc.contributor.authorAhn, Ji Hyeon-
dc.contributor.authorLee, Dae Hwan-
dc.contributor.authorYan, Bing Chun-
dc.contributor.authorPark, Joon Ha-
dc.contributor.authorKim, In Hye-
dc.contributor.authorCho, Geum-Sil-
dc.contributor.authorKim, Young-Myeong-
dc.contributor.authorLee, Bonghee-
dc.contributor.authorPark, Chan Woo-
dc.contributor.authorCho, Jun Hwi-
dc.contributor.authorLee, Hui Young-
dc.contributor.authorWon, Moo-Ho-
dc.date.available2020-02-28T23:46:34Z-
dc.date.created2020-02-06-
dc.date.issued2013-05-13-
dc.identifier.issn0006-8993-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14542-
dc.description.abstractAlthough many studies regarding ischemic brain damage in the gerbil have been reported, studies on neuronal damage according to various durations of ischemia-reperfusion (I-R) have been limited. In this study, we examined neuronal damage/death and glial changes in the somatosensory cortex 4 days after 5, 10 and 15 min of transient cerebral ischemia using the gerbil. To examine neuronal damage, we used Fluoro-jade B (F-J B, a marker for neuronal degeneration) histofluorescence staining as well as cresyl violet (CV) staining and neuronal nuclei (NeuN, neuronal marker) immunohistochemistry. In the somatosensory cortex, some CV and NeuN positive ((+)) neurons were slightly decreased only in layers III and VI in the 5 min ischemia-group, and the number of CV+ and NeuN(+) neurons were decreased with longer ischemic time. The F-J B histofluorescence staining showed a clear neuronal damage in layers III and VI, and the number of F-J B+ neurons was increased with time of ischemia-reperfusion: in the 15 min ischemia-group, the number of F-J B+ neurons was much higher in layer III than in layer VI. In addition, we immunohistochemically examined gliosis of astrocytes and microglia using anti-glial fibrillary acidic protein (GFAP) and anti-ionized calcium-binding adapter molecule 1 (Iba-1) antibody, respectively. In the 5 min ischemia-group, GFAP(+) astrocytes and Iba-1(+) microglia were distinctively increased in number, and their immunoreactivity was stronger than that in the sham-group. In the 10 and 15 min ischemia-groups, numbers of GFAP(+) and Iba-1(+) glial cells were much more increased with time of ischemia-reperfusion; in the 15 min ischemia-group, their distribution patterns of GFAP(+) and Iba-1(+) glial cells were similar to those in the 10 min ischemia-group. Our fining indicates that neuronal death/damage and gliosis of astrocytes and microglia were apparently increased with longer time of ischemia-reperfusion. (C) 2013 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfBRAIN RESEARCH-
dc.subjectFLUORO-JADE B-
dc.subjectMONGOLIAN GERBILS-
dc.subjectRAT-BRAIN-
dc.subjectSELECTIVE VULNERABILITY-
dc.subjectPYRAMIDAL NEURONS-
dc.subjectGLOBAL-ISCHEMIA-
dc.subjectVISUAL-CORTEX-
dc.subjectTIME-COURSE-
dc.subjectIN-VITRO-
dc.subjectHIPPOCAMPUS-
dc.titleNeuronal damage and gliosis in the somatosensory cortex induced by various durations of transient cerebral ischemia in gerbils-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000319304600007-
dc.identifier.doi10.1016/j.brainres.2013.03.008-
dc.identifier.bibliographicCitationBRAIN RESEARCH, v.1510, pp.78 - 88-
dc.identifier.scopusid2-s2.0-84876665995-
dc.citation.endPage88-
dc.citation.startPage78-
dc.citation.titleBRAIN RESEARCH-
dc.citation.volume1510-
dc.contributor.affiliatedAuthorLee, Bonghee-
dc.type.docTypeArticle-
dc.subject.keywordAuthorIschemia-reperfusion-
dc.subject.keywordAuthorIschemic duration-
dc.subject.keywordAuthorCerebral cortex-
dc.subject.keywordAuthorDelayed neuronal death-
dc.subject.keywordAuthorAstrocytes-
dc.subject.keywordAuthorMicroglia-
dc.subject.keywordPlusFLUORO-JADE B-
dc.subject.keywordPlusMONGOLIAN GERBILS-
dc.subject.keywordPlusRAT-BRAIN-
dc.subject.keywordPlusSELECTIVE VULNERABILITY-
dc.subject.keywordPlusPYRAMIDAL NEURONS-
dc.subject.keywordPlusGLOBAL-ISCHEMIA-
dc.subject.keywordPlusVISUAL-CORTEX-
dc.subject.keywordPlusTIME-COURSE-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusHIPPOCAMPUS-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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