Hovens Iris B, van Leeuwen Barbara L, Nyakas Csaba, Heineman Erik, van der Zee Eddy A, Schoemaker Regien G
Department of Molecular Neurobiology, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands.
Brain Physiology Unite, Semmelweis University, Üllői út 26, H-1085 Budapest, Hungary.
Neurobiol Learn Mem. 2015 Feb;118:74-9. doi: 10.1016/j.nlm.2014.11.009. Epub 2014 Nov 21.
Research indicates that neuroinflammation plays a major role in postoperative cognitive dysfunction (POCD) in older patients. However, studies have mainly focused on hippocampal neuroinflammation and hippocampal-dependent learning and memory, which does not cover the whole spectrum of POCD. We hypothesized that regional differences in postoperative neuroinflammation in the brain may underlie variation in postoperative cognitive impairment. We aimed to investigate this hypothesis in a rat-model for POCD, by analyzing postoperative impairment in behavioral task performance and microglial activation in related brain areas. We subjected 25 months old Wistar rats to surgery and assessed spatial learning and memory, object and location recognition, reversal learning and exploratory behavior in the second postoperative week. The number and morphology of microglia were analyzed in the hippocampus, prefrontal cortex, striatum and amygdala on postoperative day 14. Control groups consisted of 3 and 25 months old rats that did not undergo surgery. We observed age related impairment in learning, memory and behavior, which was aggravated following surgery. Additionally, in old rats surgery was associated with signs of classical microglial activation in brain areas related to the impaired cognitive functions. These outcomes suggest that indeed neuroinflammation may be involved in POCD. Moreover, effects of age and surgery on cognition and microglial morphology seem to be area specific and hence cannot be generalized to the whole brain. This underpins the importance for expanding the research of POCD beyond the hippocampus.
研究表明,神经炎症在老年患者术后认知功能障碍(POCD)中起主要作用。然而,研究主要集中在海马体神经炎症以及依赖海马体的学习和记忆方面,并未涵盖POCD的全貌。我们推测,大脑术后神经炎症的区域差异可能是术后认知障碍差异的基础。我们旨在通过分析行为任务表现的术后损伤以及相关脑区的小胶质细胞激活情况,在POCD大鼠模型中研究这一假设。我们对25月龄的Wistar大鼠进行手术,并在术后第二周评估其空间学习和记忆、物体及位置识别、逆向学习和探索行为。在术后第14天分析海马体、前额叶皮质、纹状体和杏仁核中小胶质细胞的数量和形态。对照组由未接受手术的3月龄和25月龄大鼠组成。我们观察到与年龄相关的学习、记忆和行为损伤,术后这种损伤会加剧。此外,在老年大鼠中,手术与认知功能受损相关脑区的经典小胶质细胞激活迹象有关。这些结果表明,神经炎症确实可能与POCD有关。此外,年龄和手术对认知及小胶质细胞形态的影响似乎具有区域特异性,因此不能推广至整个大脑。这突出了将POCD研究扩展至海马体以外区域的重要性。