Cited 57 time in
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
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Park, Sunmin | - |
| dc.contributor.author | Kim, Da Sol | - |
| dc.contributor.author | Karig, Suna | - |
| dc.contributor.author | Kim, Hyun Jin | - |
| dc.date.accessioned | 2022-12-26T16:31:28Z | - |
| dc.date.available | 2022-12-26T16:31:28Z | - |
| dc.date.issued | 2018-12 | - |
| dc.identifier.issn | 0271-5317 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/11006 | - |
| dc.description.abstract | Luteolin 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.extent | 16 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
| dc.title | 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 | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1016/j.nutres.2018.09.010 | - |
| dc.identifier.scopusid | 2-s2.0-85055745397 | - |
| dc.identifier.wosid | 000454186500012 | - |
| dc.identifier.bibliographicCitation | NUTRITION RESEARCH, v.60, pp 116 - 131 | - |
| dc.citation.title | NUTRITION RESEARCH | - |
| dc.citation.volume | 60 | - |
| dc.citation.startPage | 116 | - |
| dc.citation.endPage | 131 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Nutrition & Dietetics | - |
| dc.relation.journalWebOfScienceCategory | Nutrition & Dietetics | - |
| dc.subject.keywordPlus | NF-KAPPA-B | - |
| dc.subject.keywordPlus | GLUCOSE-HOMEOSTASIS | - |
| dc.subject.keywordPlus | PREVENTS | - |
| dc.subject.keywordPlus | BRAIN | - |
| dc.subject.keywordPlus | RESISTANCE | - |
| dc.subject.keywordPlus | EXPRESSION | - |
| dc.subject.keywordPlus | PROTECTS | - |
| dc.subject.keywordPlus | MICE | - |
| dc.subject.keywordPlus | OLIGOMERS | - |
| dc.subject.keywordPlus | QUERCETIN | - |
| dc.subject.keywordAuthor | Memory deficit | - |
| dc.subject.keywordAuthor | Metabolomics | - |
| dc.subject.keywordAuthor | Insulin signaling | - |
| dc.subject.keywordAuthor | Hippocampus | - |
| dc.subject.keywordAuthor | Norepinephrine | - |
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