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
收藏
页数:12
相关论文
共 53 条
  • [1] Bonafè M, 2001, EUR J IMMUNOL, V31, P2357, DOI 10.1002/1521-4141(200108)31:8<2357::AID-IMMU2357>3.0.CO
  • [2] 2-X
  • [3] A high plasma concentration of TNF-α is associated with dementia in centenarians
    Bruunsgaard, H
    Andersen-Ranberg, K
    Jeune, B
    Pedersen, AN
    Skinhoj, P
    Pedersen, BK
    [J]. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1999, 54 (07): : M357 - M364
  • [4] Ginsenoside Rg1 enhances the resistance of hematopoietic stem/progenitor cells to radiation-induced aging in mice
    Chen, Cui
    Mu, Xin-yi
    Zhou, Yue
    Shun, Ke
    Geng, Shan
    Liu, Jun
    Wang, Jian-wei
    Chen, Jie
    Li, Tin-yu
    Wang, Ya-ping
    [J]. ACTA PHARMACOLOGICA SINICA, 2014, 35 (01) : 143 - 150
  • [5] Ginsenoside Rg1 delays tert-butyl hydroperoxide-induced premature senescence in human WI-38 diploid fibroblast cells
    Chen, Xiaochun
    Zhang, Jing
    Fang, Yaxiu
    Zhao, Chaohui
    Zhu, Yuangui
    [J]. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2008, 63 (03): : 253 - 264
  • [6] Anti-amnestic and anti-aging effects of ginsenoside Rg1 and Rb1 and its mechanism of action
    Cheng, Y
    Shen, LH
    Zhang, JT
    [J]. ACTA PHARMACOLOGICA SINICA, 2005, 26 (02) : 143 - 149
  • [7] REACTIVE ASTROCYTES EXPRESS THE EMBRYONIC INTERMEDIATE NEUROFILAMENT NESTIN
    CLARKE, SR
    SHETTY, AK
    BRADLEY, JL
    TURNER, DA
    [J]. NEUROREPORT, 1994, 5 (15) : 1885 - 1888
  • [8] Chronic systemic D-galactose exposure induces memory loss, neuro degeneration, and oxidative damage in mice:: Protective effects of R-α-lipoic acid
    Cui, Xu
    Zuo, Pingping
    Zhang, Qing
    Li, Xuekun
    Hu, Yazhuo
    Long, Jiangang
    Packer, Lester
    Liu, Jiankang
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2006, 84 (03) : 647 - 654
  • [9] A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO
    DIMRI, GP
    LEE, XH
    BASILE, G
    ACOSTA, M
    SCOTT, C
    ROSKELLEY, C
    MEDRANO, EE
    LINSKENS, M
    RUBELJ, I
    PEREIRASMITH, O
    PEACOCKE, M
    CAMPISI, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) : 9363 - 9367
  • [10] Class III β-tubulin is constitutively coexpressed with glial fibrillary acidic protein and nestin in midgestational human fetal astrocytes:: Implications for phenotypic identity
    Draberova, Eduarda
    Del Valle, Luis
    Gordon, Jennifer
    Markova, Vladimira
    Smejkalova, Barbora
    Bertrand, Louise
    de Chadarevian, Jean-Pierre
    Agamanolis, Dimitri P.
    Legido, Agustin
    Khalili, Kamel
    Draber, Pavel
    Katsetos, Christos D.
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2008, 67 (04) : 341 - 354