Yao Zhi-Gang, Liang Liang, Liu Yu, Zhang Ling, Zhu Hua, Huang Lan, Qin Chuan
Comparative Medical Center, Institute of Laboratory Animal Science, Peking Union Medical College (PUMC) and Chinese Academy of Medical Science (CAMS), Beijing, China.
Cell Mol Neurobiol. 2014 Aug;34(6):805-12. doi: 10.1007/s10571-013-0012-y. Epub 2014 Jun 18.
Alzheimer's disease (AD) is a very common progressive neurodegenerative disorder affecting the learning and memory abilities in the brain. Key findings from recent studies of epigenetic mechanisms of memory suggest chromatin remodeling disorders via histone hypoacetylation of the lysine residue contribute to the cognitive impairment in AD. Therefore, the deinhibition of histone acetylation induced by histone deacetylases (HDACs) inhibitors contributes to recovery of learning and memory. We show here that the antiepileptic drug sodium valproate (VPA) potently enhanced long-term recognition memory and spatial learning and memory in AD transgenic mice. Possible mechanisms showed VPA could significantly elevate histone acetylation through HDACs activity inhibition and increase plasticity-associated gene expression within the hippocampi of mice. Our study suggests that VPA, serving as a HDACs inhibitor, can be considered as a potential pharmaceutical agent for the improvement of cognitive function in AD.
阿尔茨海默病(AD)是一种非常常见的进行性神经退行性疾病,会影响大脑的学习和记忆能力。近期关于记忆表观遗传机制的研究的关键发现表明,赖氨酸残基的组蛋白低乙酰化导致的染色质重塑紊乱会导致AD患者的认知障碍。因此,组蛋白去乙酰化酶(HDACs)抑制剂诱导的组蛋白乙酰化去抑制有助于学习和记忆的恢复。我们在此表明,抗癫痫药物丙戊酸钠(VPA)可有效增强AD转基因小鼠的长期识别记忆以及空间学习和记忆能力。可能的机制表明,VPA可通过抑制HDACs活性显著提高组蛋白乙酰化水平,并增加小鼠海马体内与可塑性相关的基因表达。我们的研究表明,作为一种HDACs抑制剂,VPA可被视为改善AD患者认知功能的潜在药物。