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dc.contributor.authorNam, Sung Min-
dc.contributor.authorHwang, Hongik-
dc.contributor.authorSeo, Misun-
dc.contributor.authorChang, Byung-Joon-
dc.contributor.authorKim, Hyeon-Joong-
dc.contributor.authorChoi, Sun-Hye-
dc.contributor.authorRhim, Hyewhon-
dc.contributor.authorKim, Hyoung-Chun-
dc.contributor.authorCho, Ik-Hyun-
dc.contributor.authorNah, Seung-Yeol-
dc.date.accessioned2024-01-19T22:04:24Z-
dc.date.available2024-01-19T22:04:24Z-
dc.date.created2021-09-03-
dc.date.issued2018-08-
dc.identifier.issn0304-324X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121124-
dc.description.abstractBackground: Ginseng has been used to improve brain function and increase longevity. However, little is known about the ingredients of ginseng and molecular mechanisms of its anti-brain aging effects. Gintonin is a novel exogenous ginseng-derived lysophosphatidic acid (LPA) receptor ligand; LPA and LPA1 receptors are involved in adult hippocampal neurogenesis. D-galactose (D-gal) is used to induce brain aging in animal models because long-term treatment with D-gal facilitates hippocampal aging in experimental adult animals by decreasing hippocampal neurogenesis and inducing learning and memory dysfunction. Objective: To investigate the protective effects of gintonin on D-gal-induced hippocampal senescence, impairment of long-term potentiation (LTP), and memory dysfunction. Methods: Brain hippocampal aging was induced by D-gal administration (150 mg/kg/day, s.c.; 10 weeks). From the 7th week, gintonin (50 or 100 mg/kg/day, per os) was co-administered with D-gal for 4 weeks. We performed histological analyses, LTP measurements, and object location test. Results: Co-administration of gintonin ameliorated D-gal-induced reductions in hippocampal Ki67-immunoreactive proliferating cells, doublecortin-immunoreactive neuroblasts, 5-bromo-2'-deoxyuridinein-corporating NeuN-immunoreactive mature neurons, and LPA1 receptor expression. Co-administration of gintonin in D-gal-treated mice increased the expression of phosphorylated cyclic adenosine monophosphate response element binding protein in the hippocampal dentate gyrus. In addition, co-administration of gintonin in D-gal-treated mice enhanced LTP and restored the cognitive functions compared with those in mice treated with D-gal only. Conclusion: These results show that gintonin administration restores D-gal-induced memory deficits by enhancing hippocampal LPA1 receptor expression, LTP, and neurogenesis. Finally, the present study shows that gintonin exerts anti-brain aging effects that are responsible for alleviating brain aging-related dysfunction. (C) 2018 S. Karger AG, Basel-
dc.languageEnglish-
dc.publisherS. Karger AG-
dc.titleGintonin Attenuates D-Galactose-Induced Hippocampal Senescence by Improving Long-Term Hippocampal Potentiation, Neurogenesis, and Cognitive Functions-
dc.typeArticle-
dc.identifier.doi10.1159/000491113-
dc.description.journalClass1-
dc.identifier.bibliographicCitationGerontology, v.64, no.6, pp.562 - 575-
dc.citation.titleGerontology-
dc.citation.volume64-
dc.citation.number6-
dc.citation.startPage562-
dc.citation.endPage575-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000448887300006-
dc.identifier.scopusid2-s2.0-85052744885-
dc.relation.journalWebOfScienceCategoryGeriatrics & Gerontology-
dc.relation.journalResearchAreaGeriatrics & Gerontology-
dc.type.docTypeArticle-
dc.subject.keywordPlusLYSOPHOSPHATIDIC ACID RECEPTOR-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusCELL-PROLIFERATION-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusENRICHED FRACTION-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusMULTIPLE FORMS-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusMEMORY-
dc.subject.keywordPlusGINSENG-
dc.subject.keywordAuthorGinseng-
dc.subject.keywordAuthorGintonin-
dc.subject.keywordAuthorD-galactose-
dc.subject.keywordAuthorHippocampus-
dc.subject.keywordAuthorNeurogenesis-
dc.subject.keywordAuthorBrain senescence-
dc.subject.keywordAuthorAnti-brain aging-
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