Farrell R, Evans S, Corbett D
Basic Medical Sciences, Faculty of Medicine, Memorial University, St. John's, NF, Canada A1B 3V6.
Neuroscience. 2001;107(4):585-92. doi: 10.1016/s0306-4522(01)00386-4.
Prior exposure to brief 'conditioning' episodes of ischemia protects hippocampal CA1 neurons against a subsequent more severe ischemic insult. However, protected cells exhibit abnormal function and as survival times are extended this ischemic tolerance dissipates and cells begin to die. In this study, we sought to determine whether environmental enrichment could alter the above pattern of delayed cell death and functional impairment in a gerbil model of ischemic tolerance. Gerbils received either ischemic preconditioning, 5 min of ischemia without preconditioning or sham surgery. Three days after ischemia, gerbils were placed in either an enriched environment or standard laboratory housing. Open field habituation was assessed 3, 7, 10, 30 and 60 days after ischemia. Subsequently, animals were trained in two versions (win-shift and win-stay) of a T-maze task. Following behavioral testing, extracellular CA1 field potential amplitudes and CA1 cell counts were determined. Initial open field activity was significantly higher in all experimental groups compared to sham animals (P<0.001). By 60 days, enriched ischemic preconditioned and enriched ischemic gerbils were not different than shams whereas non-enriched, ischemic preconditioned and ischemic gerbils continued to have higher activity scores (P<0.05). Preconditioned and enriched ischemic animals learned the win-shift T-maze problem as quickly as shams while non-enriched ischemic gerbils were severely impaired compared with all other groups (P<0.001). Only the sham and enriched preconditioned groups readily acquired the win-stay paradigm. CA1 field potential amplitudes were lower (P<0.05) in ischemic than sham gerbils irrespective of treatment. Surprisingly, CA1 cell counts were significantly lower (P<0.01) in enriched versus non-enriched ischemic preconditioned animals. These data demonstrate that early, intensive intervention after ischemia can improve functional outcome but that this is accompanied by increased brain damage. Careful consideration needs to be given to the timing of rehabilitation after stroke and related types of brain injury.
先前经历短暂的缺血“预处理”阶段可保护海马CA1神经元免受随后更严重的缺血损伤。然而,受保护的细胞表现出异常功能,并且随着存活时间延长,这种缺血耐受性会消失,细胞开始死亡。在本研究中,我们试图确定环境丰富化是否能改变沙鼠缺血耐受模型中上述延迟性细胞死亡和功能损伤的模式。沙鼠接受缺血预处理、5分钟无预处理缺血或假手术。缺血三天后,将沙鼠置于丰富环境或标准实验室饲养环境中。在缺血后3、7、10、30和60天评估旷场习惯化。随后,动物接受两种版本(赢-转换和赢-停留)的T迷宫任务训练。行为测试后,测定细胞外CA1场电位幅度和CA1细胞计数。与假手术动物相比,所有实验组的初始旷场活动均显著更高(P<0.001)。到60天时,丰富环境下的缺血预处理沙鼠和丰富环境下的缺血沙鼠与假手术沙鼠无异,而未丰富环境下的缺血预处理沙鼠和缺血沙鼠的活动得分仍然较高(P<0.05)。预处理且处于丰富环境的缺血动物学习赢-转换T迷宫问题的速度与假手术动物一样快,而未丰富环境下的缺血沙鼠与所有其他组相比严重受损(P<0.001)。只有假手术组和丰富环境下的预处理组能轻易学会赢-停留范式。无论治疗如何,缺血沙鼠的CA1场电位幅度均低于假手术沙鼠(P<0.05)。令人惊讶的是,丰富环境下的缺血预处理动物与未丰富环境下的相比,CA1细胞计数显著更低(P<0.01)。这些数据表明,缺血后的早期强化干预可改善功能结局,但同时伴有脑损伤增加。对于中风及相关类型脑损伤后的康复时机,需要仔细考虑。