Gintonin Attenuates D-Galactose-Induced Hippocampal Senescence by Improving Long-Term Hippocampal Potentiation, Neurogenesis, and Cognitive Functions
- Authors
- Nam, Sung Min; Hwang, Hongik; Seo, Misun; Chang, Byung-Joon; Kim, Hyeon-Joong; Choi, Sun-Hye; Rhim, Hyewhon; Kim, Hyoung-Chun; Cho, Ik-Hyun; Nah, Seung-Yeol
- Issue Date
- 2018-08
- Publisher
- S. Karger AG
- Citation
- Gerontology, v.64, no.6, pp.562 - 575
- Abstract
- Background: 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
- Keywords
- LYSOPHOSPHATIDIC ACID RECEPTOR; SYNAPTIC PLASTICITY; CELL-PROLIFERATION; ALZHEIMERS-DISEASE; ENRICHED FRACTION; OXIDATIVE STRESS; MULTIPLE FORMS; MICE; MEMORY; GINSENG; Ginseng; Gintonin; D-galactose; Hippocampus; Neurogenesis; Brain senescence; Anti-brain aging
- ISSN
- 0304-324X
- URI
- https://pubs.kist.re.kr/handle/201004/121124
- DOI
- 10.1159/000491113
- Appears in Collections:
- KIST Article > 2018
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