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The combination of luteolin and L-theanine improved Alzheimer disease-like symptoms by potentiating hippocampal insulin signaling and decreasing neuroinflammation and norepinephrine degradation in amyloid-beta-infused rats

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dc.contributor.authorPark, Sunmin-
dc.contributor.authorKim, Da Sol-
dc.contributor.authorKarig, Suna-
dc.contributor.authorKim, Hyun Jin-
dc.date.accessioned2022-12-26T16:31:28Z-
dc.date.available2022-12-26T16:31:28Z-
dc.date.issued2018-12-
dc.identifier.issn0271-5317-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/11006-
dc.description.abstractLuteolin and L-theanine have anti-inflammatory, antioxidant, and possible antidiabetic activities, and they may synergistically protect against dementia. Here, we hypothesized that a combination of luteolin and L-theanine would synergistically act to improve memory function and glucose disturbances in rats infused with amyloid-beta, and the mechanisms underlying these actions were investigated. Rats that received an amyloid-beta(25-35) infusion into the CA1 region of the hippocampus were fed dextrin (AD-CON), 0.1% luteolin (AD-Lut), 0.2% L-theanine (AD-Thea), or both 0.05% luteolin and 0.1% L-theanine (AD-LuTh) in conjunction with a high-fat diet over 8 weeks. AD-LuTh improved memory function, as determined by water maze and passive avoidance tests, by potentiating the hippocampal insulin signaling and reducing inflammation: Luteolin mainly potentiated insulin signaling via the pAkt -> pGSK -> pTau pathway, and L-theanine primarily reduced tumor necrosis factor-alpha. In the metabolomics analysis of the hippocampus lysates, the concentration of proline, phenylpyruvic acid, and normetanephrine decreased in the AD-LuTh compared to AD-CON. Norepinephrine contents were lower in the AD-CON than non-AD rats with a high fat diet with 0.2% dextrin, whereas AD-Thea and AD-LuTh inhibited the decrease. Both the AD-Lut and AD-LuTh increased glucose infusion rates and decreased hepatic glucose output under basal and hyperinsulinemic conditions, indicating improved whole-body and hepatic insulin sensitivity. Disturbances in glucose-stimulated insulin secretion during hyperglycemic clamp were most effectively corrected by the AD-Lut and AD-LuTh treatments. In conclusion, the hypothesis of the study was accepted. The combination of luteolin and L-theanine prevented Alzheimer disease-like symptom, possibly by improving hippocampal insulin signaling, norepinephrine metabolisms, and decreasing neuroinflammation. The combination of luteolin and L-theanine may be a useful therapeutic option for preventing and/or delaying the progression of memory dysfunction. (C) 2018 Elsevier Inc. All rights reserved.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleThe combination of luteolin and L-theanine improved Alzheimer disease-like symptoms by potentiating hippocampal insulin signaling and decreasing neuroinflammation and norepinephrine degradation in amyloid-beta-infused rats-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.nutres.2018.09.010-
dc.identifier.scopusid2-s2.0-85055745397-
dc.identifier.wosid000454186500012-
dc.identifier.bibliographicCitationNUTRITION RESEARCH, v.60, pp 116 - 131-
dc.citation.titleNUTRITION RESEARCH-
dc.citation.volume60-
dc.citation.startPage116-
dc.citation.endPage131-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusGLUCOSE-HOMEOSTASIS-
dc.subject.keywordPlusPREVENTS-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROTECTS-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusOLIGOMERS-
dc.subject.keywordPlusQUERCETIN-
dc.subject.keywordAuthorMemory deficit-
dc.subject.keywordAuthorMetabolomics-
dc.subject.keywordAuthorInsulin signaling-
dc.subject.keywordAuthorHippocampus-
dc.subject.keywordAuthorNorepinephrine-
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