Trinity College Institute of Neuroscience and Trinity Centre for Bioengineering, Trinity College Dublin, Dublin 2, Ireland.
J Neurosci. 2012 Mar 7;32(10):3540-51. doi: 10.1523/JNEUROSCI.6449-11.2012.
There are important and sustained interindividual differences in cognition during aging. Here, we investigated hippocampal spatial representations in a rat model of cognitive aging characterized by individual differences in a mnemonic task. Individual cognitive capabilities in old rats were assessed in a delayed non-matching-to-position task. We recorded hippocampal CA1 place cells as the rats explored a familiar environment. Unlike the usual place cells commonly described in the literature, we found that a significant fraction of pyramidal neurons recorded in our study showed a substantial delayed onset of their place field activity. We established that this firing onset delay naturally occurs under basal conditions in old rats and is positively correlated with the remapping status of the animals. The lack of firing during the first few hundred seconds after the animals were introduced into a familiar environment was also associated with an increased locomotion in the remapping rats. This delayed activity is central to understanding the individual basis of age-related cognitive impairment and to resolving numerous discrepancies in the literature on the place cell contribution to the etiology of aged-related decline. Finally, we also found a positive correlation between the degree of firing variability of place cells ("overdispersion") and performance during the long delays in the delayed non-matching-to-position task. Place cell overdispersion might provide the functional basis for interindividual differences in behavior and cognition.
在衰老过程中,认知存在重要且持续的个体间差异。在这里,我们研究了认知老化大鼠模型中海马的空间表示,该模型的特点是在记忆任务中存在个体差异。我们在延迟非匹配位置任务中评估了老年大鼠的个体认知能力。当大鼠在熟悉的环境中探索时,我们记录了 CA1 锥体神经元的位置细胞。与文献中通常描述的位置细胞不同,我们发现我们研究中记录的相当一部分锥体神经元的位置场活动存在明显的延迟起始。我们确定这种放电起始延迟在老年大鼠的基础条件下自然发生,并且与动物的重映射状态呈正相关。在动物被引入熟悉环境后的最初几百秒内缺乏放电也与重映射大鼠的运动增加有关。这种延迟活动是理解与年龄相关的认知障碍的个体基础以及解决与年龄相关下降的位置细胞贡献有关的文献中的许多差异的关键。最后,我们还发现,在延迟非匹配到位置任务中的长延迟期间,位置细胞放电变异性(“过度分散”)的程度与性能之间存在正相关。位置细胞过度分散可能为行为和认知的个体间差异提供功能基础。