Ginsenoside Rg1 Prevents Cognitive Impairment and Hippocampus Senescence in a Rat Model of D-Galactose-Induced Aging

被引:165
|
作者
Zhu, Jiahong [1 ]
Mu, Xinyi [1 ]
Zeng, Jin [2 ]
Xu, Chunyan [1 ]
Liu, Jun [1 ]
Zhang, Mengsi [1 ]
Li, Chengpeng [1 ]
Chen, Jie [3 ]
Li, Tinyu [3 ]
Wang, Yaping [1 ]
机构
[1] Chongqing Med Univ, Dept Histol & Embryol, Lab Stem Cells & Tissue Engn, Chongqing, Peoples R China
[2] Land Force Lintong Sanat, Xian, Shanxi, Peoples R China
[3] Chongqing Stem Cell Therapy Engn Tech Ctr, Chongqing, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 06期
基金
国家教育部科学基金资助; 中国国家自然科学基金;
关键词
NEURAL STEM-CELLS; DENTATE GYRUS; ADVANCED GLYCATION; DEPENDENT KINASES; OXIDATIVE DAMAGE; GENE-EXPRESSION; MEMORY LOSS; MICE; NEUROGENESIS; ASTROCYTES;
D O I
10.1371/journal.pone.0101291
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neurogenesis continues throughout the lifetime in the hippocampus, while the rate declines with brain aging. It has beenhypothesized 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-1 beta, IL-6 and TNF-alpha, which are the proinflammatory cytokines; increased the telomere lengths and telomerase activity; and down-regulated the mRNA expression of cellular senescence associated genes p53, p21(Cip1/Waf1) and p19(Arf) 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.
引用
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页数:12
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