Mental Health Institute of Quebec, Quebec City, QC, Canada G1J 2G3.
J Neurosci. 2013 Jan 23;33(4):1344-56. doi: 10.1523/JNEUROSCI.3258-12.2013.
Normal aging is associated with a variable decline in cognitive functions. Among these, executive function, decision-making, and working memory are primarily associated with the prefrontal cortex. Although a number of studies have examined the structural substrates of cognitive decline associated with aging within this cortical area, their functional correlates remain poorly understood. To fill this gap, we aimed to identify functional synaptic substrates of age-associated frontal-dependent deficits in layer 2/3 pyramidal neurons of medial prefrontal cortex of 3-, 9-, and ≥ 23-month-old Fischer 344 rats. We combined, in the same animals, novelty recognition and exploratory behavioral tasks with assessment of structural and functional aspects of prefrontal synaptic properties. We found that subsets of aged animals displayed stereotyped exploratory behavior or memory deficits. Despite an age-dependent dendritic spine loss, patch-clamp recording of synaptic activity revealed an increase in miniature EPSC frequency restricted to aged animals with preserved exploratory behavior. In contrast, we found a strong positive relationship between miniature IPSC frequency and the occurrence of both stereotyped exploratory behavior and novelty-related memory deficits. The enhanced miniature inhibitory tone was accompanied by a deficit in activity-driven inhibition, also suggesting an impaired dynamic range for modulation of inhibition in the aged, cognitively impaired animals. Together, our data indicate that differential changes in the balance of inhibitory to excitatory synaptic tone may underlie distinct trajectories in the evolution of cognitive performance during aging.
正常衰老与认知功能的不同程度下降有关。在这些认知功能中,执行功能、决策和工作记忆主要与前额叶皮层有关。尽管许多研究已经检查了与老化相关的皮质区域内认知下降的结构基础,但它们的功能相关性仍知之甚少。为了填补这一空白,我们旨在确定与年龄相关的前额叶依赖的 3、9 和≥23 个月大的 Fischer 344 大鼠内侧前额叶皮层第 2/3 层锥体神经元功能突触基质。我们在同一动物中结合了新颖性识别和探索性行为任务,以及评估前额叶突触特性的结构和功能方面。我们发现,一些老年动物表现出刻板的探索行为或记忆缺陷。尽管存在与年龄相关的树突棘丢失,但突触活动的膜片钳记录显示,仅在保持探索行为的老年动物中,微小 EPSC 频率增加。相比之下,我们发现微小 IPSC 频率与刻板探索行为和与新颖性相关的记忆缺陷的发生之间存在很强的正相关关系。增强的微小抑制性音调伴随着活性驱动抑制的缺陷,这也表明在认知受损的老年动物中,抑制的动态范围受到损害。总的来说,我们的数据表明,抑制性到兴奋性突触音调平衡的差异变化可能是认知表现随衰老演变的不同轨迹的基础。