Ginsennoside Rd Attenuates Cognitive Dysfunction in a Rat Model of Alzheimer’s Disease
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  • 作者:Juanfang Liu (1)
    Xiaodong Yan (2)
    Ling Li (1)
    Yi Zhu (1)
    Kefeng Qin (3)
    Linfu Zhou (4)
    Dong Sun (1)
    Xiaohui Zhang (5)
    Ruidong Ye (1)
    Gang Zhao (1)
  • 关键词:Ginsennoside Rd ; Alzheimer’s disease ; Cognition ; Apoptosis ; Inflammatory reaction
  • 刊名:Neurochemical Research
  • 出版年:2012
  • 出版时间:December 2012
  • 年:2012
  • 卷:37
  • 期:12
  • 页码:2738-2747
  • 全文大小:976KB
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  • 作者单位:Juanfang Liu (1)
    Xiaodong Yan (2)
    Ling Li (1)
    Yi Zhu (1)
    Kefeng Qin (3)
    Linfu Zhou (4)
    Dong Sun (1)
    Xiaohui Zhang (5)
    Ruidong Ye (1)
    Gang Zhao (1)

    1. Department of Neurology, Xijing Hospital, Fourth Military Medical University, 127 West Changle Road, Xi’an, 710032, People’s Republic of China
    2. Department of Orthopaedics, Tangdu Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
    3. Department of Neurology, University of Chicago, Chicago, IL, USA
    4. Department of Neurology, The Third Hospital of PLA, Baoji, People’s Republic of China
    5. Division of Neurology, Department of Internal Medicine, Dalian Sanatorium, Shenyang Military Region, Dalian, People’s Republic of China
  • ISSN:1573-6903
文摘
Alzheimer’s disease is a neurodegenerative disease characterized by the production of β-amyloid proteins and hyperphosphorylation of tau protein. Inflammation and apoptotic severity were highly correlated with earlier age at onset of Alzheimer’s disease and were also associated with cognitive decline. This study aims to examine whether the traditional Chinese medicine ginsennoside Rd could prevent cognitive deficit and take neuroprotective effects in β-amyloid peptide 1-0-induced rat model of Alzheimer’s disease. To produce Alzheimer’s disease animal model, aggregated β-amyloid peptide 1-0 injected into hippocampus bilaterally. Ginsennoside Rd protected their cognitive impairment and improved their memory function by daily intraperitoneal injection for 30?days consecutively. In addition, ginsennoside Rd alleviated the inflammation induced by β-amyloid peptide 1-0. Furthermore, ginsennoside Rd played a role in the down-regulation of caspase-3 proteins and reduced the apoptosis that normally followed β-amyloid peptide 1-0 injection. The results of this study showed that the pretreatment of ginsennoside Rd had neuroprotective effects in β-amyloid peptide 1-0-induced AD model rat.

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