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Glycated milk protein fermented with Lactobacillus rhamnosus ameliorates the cognitive health of mice under mild-stress condition

DC Field Value Language
dc.contributor.authorOh, Nam Su-
dc.contributor.authorJoung, Jae Yeon-
dc.contributor.authorLee, Ji Young-
dc.contributor.authorSong, Jae Gwang-
dc.contributor.authorOh, Sangnam-
dc.contributor.authorKim, Younghoon-
dc.contributor.authorKim, Hyung Wook-
dc.contributor.authorKim, Sae Hun-
dc.date.accessioned2022-06-24T00:29:34Z-
dc.date.available2022-06-24T00:29:34Z-
dc.date.created2020-11-23-
dc.date.created2020-11-23-
dc.date.issued2020-11-
dc.identifier.citationGut Microbes, Vol.11 No.6, pp.1643-1661-
dc.identifier.issn1949-0976-
dc.identifier.urihttps://hdl.handle.net/10371/183890-
dc.description.abstractThis study aimed to investigate the effects of glycated milk casein (Gc) fermented withLactobacillus rhamnosus4B15 (FGc) on the intestinal microbiota and physiological and behavioral properties in mice under chronic stress. Mice were administered Gc or FGc for 10 weeks and then exposed to unpredictable chronic mild stress (UCMS) for 7 weeks. FGc administration restored alterations of gut microbiota induced by UCMS. Moreover, FGc significantly reduced the stress-induced increase in serum corticosterone and decrease in serotonin levels. Anxiety-like behaviors induced by UCMS were also significantly decreased in the FGc group. UCMS-induced dysregulation of gene and protein expression related to neuroendocrine function, neuronal development, and inflammation, and gut-blood-brain barrier function was controlled by FGc pre-treatment. These results strongly suggest the protective effects of FGc targeting of intestinal microbiota for abnormal brain activity, which is consistent with the view that FGc plays an important role in regulating stress-related gut-brain axis disorders.-
dc.language영어-
dc.publisherLandes Bioscience-
dc.titleGlycated milk protein fermented with Lactobacillus rhamnosus ameliorates the cognitive health of mice under mild-stress condition-
dc.typeArticle-
dc.identifier.doi10.1080/19490976.2020.1756690-
dc.citation.journaltitleGut Microbes-
dc.identifier.wosid000583250900010-
dc.identifier.scopusid2-s2.0-85087534051-
dc.citation.endpage1661-
dc.citation.number6-
dc.citation.startpage1643-
dc.citation.volume11-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Younghoon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusGUT-BRAIN-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusSEROTONIN-
dc.subject.keywordPlusANXIETY-
dc.subject.keywordPlusCORTICOSTERONE-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordPlusINCREASES-
dc.subject.keywordAuthorChronic mild stress-
dc.subject.keywordAuthorbrain-gut-microbiome axis-
dc.subject.keywordAuthorcasein-
dc.subject.keywordAuthorglycation-
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