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Cited 6 time in webofscience Cited 7 time in scopus
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Protective Effects of High-Fat Diet against Murine Colitis in Association with Leptin Signaling and Gut Microbiome

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dc.contributor.authorLee, Y.-H.-
dc.contributor.authorKim, H.-
dc.contributor.authorNam, S.-
dc.contributor.authorChu, J.-R.-
dc.contributor.authorKim, J.-H.-
dc.contributor.authorLim, J.-S.-
dc.contributor.authorKim, S.-E.-
dc.contributor.authorSung, M.-K.-
dc.date.accessioned2022-12-26T06:40:29Z-
dc.date.available2022-12-26T06:40:29Z-
dc.date.issued2022-07-
dc.identifier.issn0024-3019-
dc.identifier.issn2075-1729-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/1073-
dc.description.abstractInflammatory bowel disease (IBD) is characterized by chronic intestinal-tract inflammation with dysregulated immune responses, which are partly attributable to dysbiosis. Given that diet plays a critical role in IBD pathogenesis and progression, we elucidated the effects of a high-fat diet (HFD) feeding on IBD development in relation to immune dysfunction and the gut microbiota. Five-week-old male C57BL/6J mice were fed either a normal diet (ND) or HFD for 14 weeks. The animals were further divided into ND, ND+ dextran sulfate sodium (DSS), HFD, and HFD+DSS treatment groups. The HFD+DSS mice exhibited lower body weight loss, lower disease activity in-dex, longer colon length, and increased tight-junction protein expression and goblet-cell propor-tions compared with the ND+DSS mice. The T helper (h)1 and Th17 cell populations and pro-in-flammatory cytokines involved in colitis pathogenesis were significantly more reduced in the HFD+DSS mice than in the ND+DSS mice. The HFD+DSS mice showed significantly increased serum leptin concentrations, colonic leptin receptor expression, enhanced anti-apoptotic AKT expres-sion, and reduced pro-apoptotic MAPK and Bax expression compared with the ND+DSS mice, sug-gesting the involvement of the leptin-mediated pathway in intestinal epithelial cell apoptosis. The alterations in the gut-microbiota composition in the HFD+DSS group were the opposite of those in the ND+DSS group and rather similar to those of the ND group, indicating that the protective effects of HFD feeding against DSS-induced colitis are associated with changes in gut-microbiota compo-sition. Overall, HFD feeding ameliorates DSS-induced colitis and colonic mucosal damage by rein-forcing colonic barrier function and regulating immune responses in association with changes in gut-microbiota composition. ? 2022 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleProtective Effects of High-Fat Diet against Murine Colitis in Association with Leptin Signaling and Gut Microbiome-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/life12070972-
dc.identifier.scopusid2-s2.0-85133501525-
dc.identifier.wosid000832128100001-
dc.identifier.bibliographicCitationLife, v.12, no.7-
dc.citation.titleLife-
dc.citation.volume12-
dc.citation.number7-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaLife Sciences & Biomedicine - Other Topics-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusULCERATIVE-COLITIS-
dc.subject.keywordPlusEPITHELIAL-CELLS-
dc.subject.keywordPlusBARRIER FUNCTION-
dc.subject.keywordPlusSERUM LEPTIN-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusDIVERSITY-
dc.subject.keywordPlusHEALTH-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthorcolonic barrier function-
dc.subject.keywordAuthorgut microbiota-
dc.subject.keywordAuthorhigh-fat diet-
dc.subject.keywordAuthorimmune response-
dc.subject.keywordAuthorinflammatory bowel disease-
dc.subject.keywordAuthorintestinal epithelial cell-
dc.subject.keywordAuthorleptin-
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