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Myeloid sirtuinl deficiency aggravates hippocampal inflammation in mice fed high-fat diets

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dc.contributor.authorKim, Kyung Eun-
dc.contributor.authorJeong, Eun Ae-
dc.contributor.authorLee, Jong Youl-
dc.contributor.authorYi, Chin-ok-
dc.contributor.authorPark, Kyung-ah-
dc.contributor.authorJin, Zhen-
dc.contributor.authorLee, Jung Eun-
dc.contributor.authorHorvath, Tamas L.-
dc.contributor.authorRoh, Gu Seob-
dc.date.accessioned2022-12-26T17:02:12Z-
dc.date.available2022-12-26T17:02:12Z-
dc.date.issued2018-05-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/11641-
dc.description.abstractChronic low-grade inflammation-induced insulin resistance is associated with neuroinflammation. Myeloid sirtuinl (SIRTI) deficiency aggravates high-fat diet (HFD)-induced insulin resistance. However, the function of myeloid-specific SIRTI in the hippocampus of obese mice is largely unknown. To address this question, we fed myeloid SIRTI knockout (KO) mice a HFD for 40 weeks. We found that HFD-fed SIRTI KO mice had increased insulin resistance and macrophage infiltration in adipose tissue than wild type (WT) mice. Levels of HFD-induced lipocalin-2 (LCN2) were lower in SIRT1 KO mice than in WT. HFD-induced hippocampal LCN2 expression was lower in HFD-fed SIRTI KO mice than in WT. Hippocampal acetylation of nuclear factor-kappa B (NF-kappa B) and amyloid precursor protein levels were higher in HFD-fed SIRT1 KO mice than in HFD-fed WT mice. Taken together, our results suggest that targeted induction of the anti-inflammatory effects of SIRTI and LCN2 may help prevent obesity-associated insulin resistance and neuroinflammation. (C) 2018 Elsevier Inc. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleMyeloid sirtuinl deficiency aggravates hippocampal inflammation in mice fed high-fat diets-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2018.04.044-
dc.identifier.scopusid2-s2.0-85045119035-
dc.identifier.wosid000431286300046-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, v.499, no.4, pp 1025 - 1031-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.volume499-
dc.citation.number4-
dc.citation.startPage1025-
dc.citation.endPage1031-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusPROTEIN LIPOCALIN 2-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusCALORIC RESTRICTION-
dc.subject.keywordPlusINSULIN-RESISTANCE-
dc.subject.keywordPlusHEPATIC STEATOSIS-
dc.subject.keywordPlusMEMORY DEFICIT-
dc.subject.keywordPlusSIRT1-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorObesity-
dc.subject.keywordAuthorSIRT1-
dc.subject.keywordAuthorLipocalin-2-
dc.subject.keywordAuthorInsulin resistance-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorHippocampus-
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