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Comparison of Expression of Inflammatory Cytokines in the Spinal Cord Between Young Adult and Aged Beagle Dogs

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dc.contributor.authorLee, Dae Hwan-
dc.contributor.authorAhn, Ji Hyeon-
dc.contributor.authorPark, Joon Ha-
dc.contributor.authorYan, Bing Chun-
dc.contributor.authorCho, Jeong-Hwi-
dc.contributor.authorKim, In Hye-
dc.contributor.authorLee, Jae-Chul-
dc.contributor.authorJang, Sang-Hun-
dc.contributor.authorLee, Myoung Hyo-
dc.contributor.authorHwang, In Koo-
dc.contributor.authorMoon, Seung Myung-
dc.contributor.authorLee, Bonghee-
dc.contributor.authorCho, Jun Hwi-
dc.contributor.authorShin, Hyung-Cheul-
dc.contributor.authorKim, Jin Sang-
dc.contributor.authorWon, Moo-Ho-
dc.date.available2020-02-28T23:44:32Z-
dc.date.created2020-02-06-
dc.date.issued2013-07-
dc.identifier.issn0272-4340-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14449-
dc.description.abstractAging is an inevitable process that occurs in the whole body system accompanying with many functional and morphological changes. Inflammation is known as one of age-related factors, and inflammatory changes could enhance mortality risk. In this study, we compared immunoreactivities of inflammatory cytokines, such as interleukin (IL)-2 (a pro-inflammatory cytokine), its receptor (IL-2R), IL-4 (an anti-inflammatory cytokine), and its receptor (IL-4R) in the cervical and lumbar spinal cord of young adult (2-3 years old) and aged (10-12 years old) beagle dogs using immunohistochemistry and western blotting. IL-2 and IL-2R-immunoreactive nerve cells were found throughout the gray matter of the cervical and lumbar spinal cord of young adult and aged dogs. In the spinal cord neurons of the aged dog, immunoreactivity and protein levels were apparently increased compared with those in the young adult dog. Change patterns of IL-4- and IL-4R-immunoreactive cells and their protein levels were also similar to those in IL-2 and IL-2R; however, IL-4 and IL-4R immunoreactivity in the periphery of the neuronal cytoplasm in the aged dog was much stronger than that in the young adult dog. These results indicate that the increase of inflammatory cytokines and their receptors in the aged spinal cord might be related to maintaining a balance of inflammatory reaction in the spinal cord during normal aging.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER/PLENUM PUBLISHERS-
dc.relation.isPartOfCELLULAR AND MOLECULAR NEUROBIOLOGY-
dc.subjectHIPPOCAMPAL CA1 REGION-
dc.subjectGROWTH-FACTOR-BETA-
dc.subjectMULTIPLE-SCLEROSIS-
dc.subjectRAT HIPPOCAMPUS-
dc.subjectNITRIC-OXIDE-
dc.subjectINJURY-
dc.subjectMICROGLIA-
dc.subjectBRAIN-
dc.subjectCNS-
dc.subjectINTERLEUKIN-4-
dc.titleComparison of Expression of Inflammatory Cytokines in the Spinal Cord Between Young Adult and Aged Beagle Dogs-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000319746400003-
dc.identifier.doi10.1007/s10571-013-9915-x-
dc.identifier.bibliographicCitationCELLULAR AND MOLECULAR NEUROBIOLOGY, v.33, no.5, pp.615 - 624-
dc.identifier.scopusid2-s2.0-84878685648-
dc.citation.endPage624-
dc.citation.startPage615-
dc.citation.titleCELLULAR AND MOLECULAR NEUROBIOLOGY-
dc.citation.volume33-
dc.citation.number5-
dc.contributor.affiliatedAuthorLee, Bonghee-
dc.type.docTypeArticle-
dc.subject.keywordAuthorAging-
dc.subject.keywordAuthorNeuroinflammation-
dc.subject.keywordAuthorInterleukins-
dc.subject.keywordAuthorSpinal gray matter-
dc.subject.keywordAuthorSpinal neurons-
dc.subject.keywordPlusHIPPOCAMPAL CA1 REGION-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusMULTIPLE-SCLEROSIS-
dc.subject.keywordPlusRAT HIPPOCAMPUS-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusMICROGLIA-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusCNS-
dc.subject.keywordPlusINTERLEUKIN-4-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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