Neurobiology Laboratory and National Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing, People's Republic of China.
J Alzheimers Dis. 2010;20(4):1143-57. doi: 10.3233/JAD-2010-091234.
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-beta(25-35) (Abeta(25-35)) or Abeta(1-42) in primary cultured hippocampal neurons of rats. Moreover, Gal(2-11) (an agonist of GalR(2/3)) also inhibited the neurotoxicity induced by Abeta(25-35) in the cultured neurons. We further found that galanin inhibited the activation of p53, Bax, and caspase-3 induced by Abeta(25-35) in the cultured hippocampal neurons. Moreover, galanin reversed the down regulation of Bcl-2 induced by Abeta(25-35) in the cultured neurons. Interestingly, in the Morris water maze task we found that intra-CA1 injection of Abeta(25-35)-induced spatial learning deficits in rats were blocked by galanin. In addition, galanin inhibited the Abeta(25-35)-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.
神经肽甘丙肽及其受体在与阿尔茨海默病(AD)相关的大脑中被发现上调,而甘丙肽在 AD 中的作用仍不清楚。本研究旨在探讨甘丙肽在体外和体内的神经保护作用。我们的结果表明,甘丙肽抑制了原代培养的大鼠海马神经元中由淀粉样β肽(25-35)(Abeta(25-35))或 Abeta(1-42)引起的神经毒性。此外,甘丙肽类似物 Gal(2-11)(GalR(2/3)的激动剂)也抑制了培养神经元中由 Abeta(25-35)引起的神经毒性。我们进一步发现,甘丙肽抑制了 Abeta(25-35)诱导的培养海马神经元中 p53、Bax 和 caspase-3 的激活。此外,甘丙肽逆转了 Abeta(25-35)诱导的培养神经元中 Bcl-2 的下调。有趣的是,在 Morris 水迷宫任务中,我们发现 Abeta(25-35)在 CA1 内注射引起的大鼠空间学习缺陷被甘丙肽阻断。此外,甘丙肽抑制了 Abeta(25-35)诱导的大鼠海马 p53、Bax 和 MAP2 的失调。我们的研究结果有力地证明了甘丙肽在神经细胞和 AD 诱导的学习和记忆缺陷中发挥神经保护作用。