| Literature DB >> 26890737 |
Xiao-Ping Hong1, Tao Chen1, Ni-Na Yin1, Yong-Ming Han1, Fang Yuan2, Yan-Jun Duan1, Feng Shen3, Yan-Hong Zhang1, Ze-Bin Chen1.
Abstract
Enhanced neurogenesis has been reported in the hippocampus of patients with Alzheimer's disease (AD), the most common neurodegenerative disorder characterized with amyloid-β (Aβ) aggregation, tau hyperphosphorylation, and progressive neuronal loss. Previously we reported that tau phosphorylation played an essential role in adult hippocampal neurogenesis, and activation of glycogen synthase kinase (GSK-3), a crucial tau kinase, could induce increased hippocampal neurogenesis. In the present study, we found that treatment of D-galactose rats with Puerarin could significantly improve behavioral performance and ameliorate the enhanced neurogenesis and microtubule-associated protein tau hyperphosphorylation in the hippocampus of D-galactose rat brains. FGF-2/GSK-3 signaling pathway might be involved in the effects of Puerarin on hippocampal neurogenesis and tau hyperphosphorylation. Our finding provides primary in vivo evidence that Puerarin can attenuate AD-like enhanced hippocampal neurogenesis and tau hyperphosphorylation. Our finding also suggests Puerarin can be served as a treatment for age-related neurodegenerative disorders, such as AD.Entities:
Keywords: Alzheimer’s disease; Puerarin; glycogen synthase kinase; hippocampus; neurogenesis; spatial memory; tau hyperphosphorylation
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Year: 2016 PMID: 26890737 DOI: 10.3233/JAD-150566
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472