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人参皂苷Rg1可预防D-半乳糖诱导的大鼠衰老模型中的认知障碍和海马衰老。

Ginsenoside Rg1 prevents cognitive impairment and hippocampus senescence in a rat model of D-galactose-induced aging.

作者信息

Zhu Jiahong, Mu Xinyi, Zeng Jin, Xu Chunyan, Liu Jun, Zhang Mengsi, Li Chengpeng, Chen Jie, Li Tinyu, Wang Yaping

机构信息

Department of Histology and Embryology, Laboratory of Stem Cells and Tissue Engineering, Chongqing Medical University, Chongqing, China.

The Land Force Lintong Sanatorium, Xi'an, Shanxi, China.

出版信息

PLoS One. 2014 Jun 30;9(6):e101291. doi: 10.1371/journal.pone.0101291. eCollection 2014.

Abstract

Neurogenesis continues throughout the lifetime in the hippocampus, while the rate declines with brain aging. It has been hypothesized that reduced neurogenesis may contribute to age-related cognitive impairment. Ginsenoside Rg1 is an active ingredient of Panax ginseng in traditional Chinese medicine, which exerts anti-oxidative and anti-aging effects. This study explores the neuroprotective effect of ginsenoside Rg1 on the hippocampus of the D-gal (D-galactose) induced aging rat model. Sub-acute aging was induced in male SD rats by subcutaneous injection of D-gal (120 mg/kg·d) for 42 days, and the rats were treated with ginsenoside Rg1 (20 mg/kg·d, intraperitoneally) or normal saline for 28 days after 14 days of D-gal injection. In another group, normal male SD rats were treated with ginsenoside Rg1 alone (20 mg/kg·d, intraperitoneally) for 28 days. It showed that administration of ginsenoside Rg1 significantly attenuated all the D-gal-induced changes in the hippocampus, including cognitive capacity, senescence-related markers and hippocampal neurogenesis, compared with the D-gal-treated rats. Further investigation showed that ginsenoside Rg1 protected NSCs/NPCs (neural stem cells/progenitor cells) shown by increased level of SOX-2 expression; reduced astrocytes activation shown by decrease level of Aeg-1 expression; increased the hippocampal cell proliferation; enhanced the activity of the antioxidant enzymes GSH-Px (glutathione peroxidase) and SOD (Superoxide Dismutase); decreased the levels of IL-1β, IL-6 and TNF-α, which are the proinflammatory cytokines; increased the telomere lengths and telomerase activity; and down-regulated the mRNA expression of cellular senescence associated genes p53, p21Cip1/Waf1 and p19Arf in the hippocampus of aged rats. Our data provides evidence that ginsenoside Rg1 can improve cognitive ability, protect NSCs/NPCs and promote neurogenesis by enhancing the antioxidant and anti-inflammatory capacity in the hippocampus.

摘要

神经发生在海马体中会持续一生,但其速率会随着大脑衰老而下降。据推测,神经发生减少可能导致与年龄相关的认知障碍。人参皂苷Rg1是传统中药人参中的一种活性成分,具有抗氧化和抗衰老作用。本研究探讨人参皂苷Rg1对D-半乳糖(D-galactose)诱导的衰老大鼠模型海马体的神经保护作用。通过皮下注射D-半乳糖(120mg/kg·d)持续42天诱导雄性SD大鼠亚急性衰老,在注射D-半乳糖14天后,大鼠接受人参皂苷Rg1(20mg/kg·d,腹腔注射)或生理盐水治疗28天。在另一组中,正常雄性SD大鼠单独接受人参皂苷Rg1(20mg/kg·d,腹腔注射)治疗28天。结果显示,与D-半乳糖处理的大鼠相比,给予人参皂苷Rg1显著减轻了D-半乳糖诱导的海马体所有变化,包括认知能力、衰老相关标志物和海马体神经发生。进一步研究表明,人参皂苷Rg1保护神经干细胞/神经祖细胞(NSCs/NPCs)表现为SOX-2表达水平增加;降低Aeg-1表达水平显示星形胶质细胞活化减少;增加海马体细胞增殖;增强抗氧化酶谷胱甘肽过氧化物酶(GSH-Px)和超氧化物歧化酶(SOD)的活性;降低促炎细胞因子IL-1β、IL-6和TNF-α的水平;增加端粒长度和端粒酶活性;并下调老年大鼠海马体中细胞衰老相关基因p53、p21Cip1/Waf1和p19Arf的mRNA表达。我们的数据提供了证据表明人参皂苷Rg1可以通过增强海马体中的抗氧化和抗炎能力来改善认知能力、保护神经干细胞/神经祖细胞并促进神经发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a1c/4076296/d930e797cca8/pone.0101291.g001.jpg

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