Systemic injection of LPS induces region-specific neuroinflammation and mitochondrial dysfunction in normal mouse brain
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Noh, Haneul | - |
dc.contributor.author | Jeon, Jeha | - |
dc.contributor.author | Seo, Hyemyung | - |
dc.date.accessioned | 2021-06-22T23:44:33Z | - |
dc.date.available | 2021-06-22T23:44:33Z | - |
dc.date.created | 2021-01-21 | - |
dc.date.issued | 2014-04 | - |
dc.identifier.issn | 0197-0186 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/23323 | - |
dc.description.abstract | Lipopolysaccharide (LPS) administration may be used to induce an in vivo model for neuroinflammation or neurodegeneration. We examined the regional distribution of inflammatory markers induced by LPS in the brain of young mice. Criteria for inflammation included measures of cytokines and microglial activation. Levels of IL-1 beta mRNA increased in the frontal cortex, parietal cortex, hippocampus, and striatum following systemic treatment with LPS. Levels of SRA mRNA increased in the frontal cortex and striatum and levels of TLR2 and TLR4 mRNAs increased in the frontal cortex and cerebellum. Iba1-positive microglial cells increased in the striatum, medial septum, frontal cortex, and hippocampus after LPS treatment. In addition, glutathione (GSH) levels decreased and mitochondrial complex II/III activities increased after systemic LPS injection. Although LPS treatment did not significantly alter cellular ATP levels, these levels correlated with levels of IL-1 beta and TLR4 in the LPS-treated mice. The region-specific inflammatory response to LPS in the brain may serve to create a model for studies of neurodegenerative disease. (C) 2014 Elsevier Ltd. All rights reserved. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | Elsevier BV | - |
dc.title | Systemic injection of LPS induces region-specific neuroinflammation and mitochondrial dysfunction in normal mouse brain | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Seo, Hyemyung | - |
dc.identifier.doi | 10.1016/j.neuint.2014.02.008 | - |
dc.identifier.scopusid | 2-s2.0-84897388280 | - |
dc.identifier.wosid | 000334985300006 | - |
dc.identifier.bibliographicCitation | Neurochemistry International, v.69, pp.35 - 40 | - |
dc.relation.isPartOf | Neurochemistry International | - |
dc.citation.title | Neurochemistry International | - |
dc.citation.volume | 69 | - |
dc.citation.startPage | 35 | - |
dc.citation.endPage | 40 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.subject.keywordPlus | MICROGLIAL ACTIVATION | - |
dc.subject.keywordPlus | INFLAMMATORY RESPONSE | - |
dc.subject.keywordPlus | LIPOPOLYSACCHARIDE | - |
dc.subject.keywordPlus | MICE | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | MODEL | - |
dc.subject.keywordPlus | DEATH | - |
dc.subject.keywordPlus | NEUROTOXICITY | - |
dc.subject.keywordPlus | MODULATION | - |
dc.subject.keywordPlus | IL-1-BETA | - |
dc.subject.keywordAuthor | LPS | - |
dc.subject.keywordAuthor | Mitochondrial dysfunction | - |
dc.subject.keywordAuthor | Neuroinflammation | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0197018614000382?via%3Dihub | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
55 Hanyangdeahak-ro, Sangnok-gu, Ansan, Gyeonggi-do, 15588, Korea+82-31-400-4269 sweetbrain@hanyang.ac.kr
COPYRIGHT © 2021 HANYANG UNIVERSITY. ALL RIGHTS RESERVED.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.