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Agmatine inhibits hypoxia-induced TNF-alpha release from cultured retinal ganglion cells

DC Field Value Language
dc.contributor.author성공제-
dc.contributor.author홍사민-
dc.contributor.author김찬윤-
dc.date.accessioned2015-05-19T16:45:27Z-
dc.date.available2015-05-19T16:45:27Z-
dc.date.issued2008-
dc.identifier.issn0327-9545-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/106888-
dc.description.abstractThe effect of hypoxia on the release of tumor necrosis factor-alpha (TNF-alpha) in transformed rat retinal ganglion cells (RGCs) and the effect of agmatine on the hypoxia-induced production of TNF-alpha in RGCs were evaluated. RGCs were cultured under hypoxic conditions with 5% oxygen, with or without 100 microM agmatine. The expression levels of TNF-alpha and its receptor-1 (TNF-R1) were investigated by Western blot analysis. After 6 hours of hypoxia, we noted an increase in TNF-alpha production in RGCs. Agmatine significantly reduced TNF-alpha level after 12 hours of hypoxic treatment. The expression of TNF-R1 was not affected by the hypoxia or agmatine treatment. Our results show that agmatine inhibits the TNF-alpha production of RGCs in hypoxic condition. These results demonstrate a possible neuroprotective mechanism for agmatine against hypoxic damage in RGCs.-
dc.description.statementOfResponsibilityopen-
dc.format.extent201~205-
dc.relation.isPartOfBIOCELL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAgmatine/pharmacology*-
dc.subject.MESHAnimals-
dc.subject.MESHCell Hypoxia*-
dc.subject.MESHCells, Cultured-
dc.subject.MESHRats-
dc.subject.MESHRats, Sprague-Dawley-
dc.subject.MESHRetinal Ganglion Cells/cytology-
dc.subject.MESHRetinal Ganglion Cells/drug effects*-
dc.subject.MESHRetinal Ganglion Cells/metabolism-
dc.subject.MESHTumor Necrosis Factor-alpha/metabolism*-
dc.titleAgmatine inhibits hypoxia-induced TNF-alpha release from cultured retinal ganglion cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Ophthalmology (안과학)-
dc.contributor.googleauthorSamin Hong-
dc.contributor.googleauthorKyoungsoo Park-
dc.contributor.googleauthorChan Yun Kim-
dc.contributor.googleauthorGong Je Seong-
dc.identifier.doi18825914-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01946-
dc.contributor.localIdA04395-
dc.contributor.localIdA01035-
dc.relation.journalcodeJ00280-
dc.identifier.eissn1667-5746-
dc.identifier.pmid18825914-
dc.identifier.urlhttp://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-95452008000200006-
dc.subject.keywordAgmatine/pharmacology*-
dc.subject.keywordAnimals-
dc.subject.keywordCell Hypoxia*-
dc.subject.keywordCells, Cultured-
dc.subject.keywordRats-
dc.subject.keywordRats, Sprague-Dawley-
dc.subject.keywordRetinal Ganglion Cells/cytology-
dc.subject.keywordRetinal Ganglion Cells/drug effects*-
dc.subject.keywordRetinal Ganglion Cells/metabolism-
dc.subject.keywordTumor Necrosis Factor-alpha/metabolism*-
dc.contributor.alternativeNameSeong, Gong Je-
dc.contributor.alternativeNameHong, Sa Min-
dc.contributor.alternativeNameKim, Chan Yun-
dc.contributor.affiliatedAuthorSeong, Gong Je-
dc.contributor.affiliatedAuthorHong, Sa Min-
dc.contributor.affiliatedAuthorKim, Chan Yun-
dc.rights.accessRightsnot free-
dc.citation.volume32-
dc.citation.number2-
dc.citation.startPage201-
dc.citation.endPage205-
dc.identifier.bibliographicCitationBIOCELL, Vol.32(2) : 201-205, 2008-
dc.identifier.rimsid50916-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers

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