Rönnbäck Annica, Dahlqvist Per, Svensson Per-Arne, Jernås Margareta, Carlsson Björn, Carlsson Lena M S, Olsson Tommy
Department of Public Health and Clinical Medicine, Umeå University Hospital, S-901 85 Umeå, Sweden.
Neurosci Lett. 2005 Sep 9;385(2):173-8. doi: 10.1016/j.neulet.2005.05.016.
Functional recovery after experimental stroke in rats is enhanced by environmental enrichment by stimulating plastic changes in brain regions outside the lesion, but the molecular mechanisms are not known. We investigated the effect of environmental enrichment after focal cerebral ischemia on cognitive recovery and hippocampal gene expression using microarray analysis. Rats placed in enriched environment (EE) for 1 month after middle cerebral artery occlusion (MCAo) showed significantly improved spatial memory in the Morris water maze compared to rats housed alone after MCAo. Microarray analysis suggested several EE-induced differences in neuronal plasticity-related genes, but these changes could not be confirmed by quantitative real-time PCR. This study highlights some of the potential problems associated with gene expression profiling of brain tissues. Further studies at earlier time points and in additional subregions of the brain are of interest in the search for molecular mechanisms behind EE-induced neuronal plasticity after ischemic stroke.
通过刺激损伤外脑区的可塑性变化,环境富集可增强大鼠实验性中风后的功能恢复,但分子机制尚不清楚。我们使用微阵列分析研究了局灶性脑缺血后环境富集对认知恢复和海马基因表达的影响。与大脑中动脉闭塞(MCAo)后单独饲养的大鼠相比,MCAo后置于富集环境(EE)中1个月的大鼠在莫里斯水迷宫中的空间记忆有显著改善。微阵列分析表明,EE诱导了一些与神经元可塑性相关基因的差异,但这些变化无法通过定量实时PCR得到证实。本研究突出了与脑组织基因表达谱相关的一些潜在问题。在寻找缺血性中风后EE诱导的神经元可塑性背后的分子机制方面,在更早的时间点和大脑的其他亚区域进行进一步研究很有意义。