Affiliations: Neurobiology Laboratory and National Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing, People's Republic of China
Correspondence:
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Correspondence to: Long-Chuan Yu, Neurobiology Laboratory and National Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing 100871, People's Republic of China. Tel.: +86 10 6275 3667; Fax: +86 10 6275 1526; E-mail: yulc@pku.edu.cn.
Note: [] Handling Associate Editor: Shengdi Chen
Abstract: The neuropeptide galanin and its receptors are found to be upregulated in brain associated with Alzheimer's disease (AD), while the role of galanin in AD is still unclear. The present study was performed to explore the neuroprotective role of galanin both in vitro and in vivo. Our results demonstrated that galanin inhibited the neurotoxicity induced by amyloid-β25-35 (Aβ25-35) or Aβ1-42 in primary cultured hippocampal neurons of rats. Moreover, Gal2-11 (an agonist of GalR2/3) also inhibited the neurotoxicity induced by Aβ25-35 in the cultured neurons. We further found that galanin inhibited the activation of p53, Bax, and caspase-3 induced by Aβ25-35 in the cultured hippocampal neurons. Moreover, galanin reversed the down regulation of Bcl-2 induced by Aβ25-35 in the cultured neurons. Interestingly, in the Morris water maze task we found that intra-CA1 injection of Aβ25-35-induced spatial learning deficits in rats were blocked by galanin. In addition, galanin inhibited the Aβ25-35-induced dysregulation of p53, Bax, and MAP2 in rat hippocampus. Our results strongly demonstrate that galanin plays neuroprotective roles in nerve cells and in AD-induced learning and memory deficits.
