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Cited 26 time in webofscience Cited 26 time in scopus
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High-fat diet-induced obesity exacerbates kainic acid-induced hippocampal cell death

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dc.contributor.authorKang, Dong Ho-
dc.contributor.authorHeo, Rok Won-
dc.contributor.authorYi, Chin-ok-
dc.contributor.authorKim, Hwajin-
dc.contributor.authorChoi, Chang Hwa-
dc.contributor.authorRoh, Gu Seob-
dc.date.accessioned2022-12-26T21:31:16Z-
dc.date.available2022-12-26T21:31:16Z-
dc.date.issued2015-10-
dc.identifier.issn1471-2202-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/16959-
dc.description.abstractBackground: Obesity has deleterious effects on the brain, and metabolic dysfunction may exacerbate the outcomes of seizures and brain injuries. However, it is unclear whether obesity affects excitotoxicity-induced neuronal cell death. The purpose of this study was to investigate the effects of a high-fat diet (HFD) on neuroinflammation and oxidative stress in the hippocampus of kainic acid (KA)-treated mice. Results: Mice were fed with a HFD or normal diet for 8 weeks and then received a systemic injection of KA. HFD-fed mice showed hypercholesterolemia, insulin resistance, and hepatic steatosis. HFD-fed mice showed greater susceptibility to KA-induced seizures, an increased number of terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-positive cells, neuroinflammation, and oxidative stress. Furthermore, we found that KA treatment increased HFD-induced calpain1, nuclear factor E2-related factor 2, and heme oxygenase-1 expression in the hippocampus. Conclusions: These findings imply that complex mechanisms affected by obesity-induced systemic inflammation, neuroinflammation, ER stress, calcium overload, and oxidative stress may contribute to neuronal death after brain injury.-
dc.language영어-
dc.language.isoENG-
dc.publisherBioMed Central-
dc.titleHigh-fat diet-induced obesity exacerbates kainic acid-induced hippocampal cell death-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1186/s12868-015-0202-2-
dc.identifier.scopusid2-s2.0-84945547939-
dc.identifier.wosid000363736000001-
dc.identifier.bibliographicCitationBMC Neuroscience, v.16, no.1-
dc.citation.titleBMC Neuroscience-
dc.citation.volume16-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusENDOPLASMIC-RETICULUM STRESS-
dc.subject.keywordPlusINSULIN-RESISTANCE-
dc.subject.keywordPlusMITOCHONDRIAL-FUNCTION-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusRAT-BRAIN-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusNRF2-
dc.subject.keywordPlusNEUROINFLAMMATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordAuthorObesity-
dc.subject.keywordAuthorExcitotoxicity-
dc.subject.keywordAuthorNeuroinflammation-
dc.subject.keywordAuthorOxidative stress-
dc.subject.keywordAuthorHippocampus-
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