Shen Jun, Xu Linling, Qu Chujie, Sun Huimin, Zhang Junjian
Department of Neurology, Zhongnan Hospital, Wuhan University, No.169, Donghu Road, Wuhan 430071, Hubei, China.
Department of Neurology, Zhongnan Hospital, Wuhan University, No.169, Donghu Road, Wuhan 430071, Hubei, China.
Behav Brain Res. 2018 Sep 3;349:1-7. doi: 10.1016/j.bbr.2018.04.050. Epub 2018 Apr 30.
Chronic unpredictable mild stress (CUMS) leads to neuropsychiatric disorders, such as depression, anxiety and cognitive impairment. Resveratrol is a natural polyphenol existed in polygonum cuspidatum and has been demonstrated to be a potent activator of Sirtuin 1 (Sirt1). Previous studies reported that resveratrol treatment ameliorated CUMS-induced depressive-like behavior and cognitive deficits through upregulating cAMP response element-binding protein (CREB) and brain derived neurotrophic factor (BDNF) expression. However, the upstream signalling pathway mediating CREB/BDNF expression and then exerting a protective role on cognitive function remains unclear. The present study aims to investigate the possible mechanism of resveratrol on CUMS-induced cognitive deficits. Male Sprague Dawley rats were adminstrated resveratrol (40 and 80 mg/kg) every day for 4 consecutive weeks before exposure to CUMS procedure. Morris Water Maze test was used to appraise spatial learing and memory of rats. Sirt1/miR-134 signalling pathway and CREB/BDNF expression in hippocampus of rats were measured. We also explored Sirt1/miR-134 signalling pathway and CREB/BDNF expression in primary cultured hippocampus neurons with resveratrol (25, 50 and 100 μmol/L) treatment. We found that resveratrol treatment prevented spatial learing and memory impairment induced by CUMS. Meanwhile the potential mechanism of resveratrol was associated with increased levels of Sirt1, CREB phosphorylation (p-CREB), CREB, BDNF and decreased levels of miR-134 in vivo and in vitro. In conclusion, our study showed that the neuroprotective effect of resveratrol on CUMS-induced cognitive impairment may rely on activating Sirt1/miR-134 pathway and then upregulating its downstream CREB/BDNF expression in hippocampus.
慢性不可预测性轻度应激(CUMS)会导致神经精神疾病,如抑郁症、焦虑症和认知障碍。白藜芦醇是一种存在于虎杖中的天然多酚,已被证明是沉默信息调节因子1(Sirt1)的有效激活剂。先前的研究报道,白藜芦醇治疗可通过上调环磷腺苷反应元件结合蛋白(CREB)和脑源性神经营养因子(BDNF)的表达来改善CUMS诱导的抑郁样行为和认知缺陷。然而,介导CREB/BDNF表达并随后对认知功能发挥保护作用的上游信号通路仍不清楚。本研究旨在探讨白藜芦醇对CUMS诱导的认知缺陷的可能机制。在暴露于CUMS程序之前,雄性Sprague Dawley大鼠连续4周每天给予白藜芦醇(40和80mg/kg)。采用Morris水迷宫试验评估大鼠的空间学习和记忆能力。检测大鼠海马中Sirt1/miR-134信号通路及CREB/BDNF的表达。我们还探讨了用白藜芦醇(25、50和100μmol/L)处理原代培养海马神经元时Sirt1/miR-134信号通路及CREB/BDNF的表达。我们发现白藜芦醇治疗可预防CUMS诱导的空间学习和记忆障碍。同时,白藜芦醇的潜在机制与体内外Sirt1、CREB磷酸化(p-CREB)、CREB、BDNF水平升高以及miR-134水平降低有关。总之,我们的研究表明,白藜芦醇对CUMS诱导的认知障碍的神经保护作用可能依赖于激活Sirt1/miR-134通路,然后上调其下游海马中CREB/BDNF的表达。