Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada.
Neurobiol Aging. 2012 Jul;33(7):1466-80. doi: 10.1016/j.neurobiolaging.2010.10.011. Epub 2010 Dec 15.
It is well established that the cerebral cortex undergoes extensive remodeling in aging. In this study, we used behaviorally characterized rats to correlate age-related morphological changes with cognitive impairment. For this, young and aged animals were tested in the Morris water maze to evaluate their cognitive performance. Following behavioral characterization, the animals were perfused and a combination of intracellular labeling and immunohistochemistry was applied. Using this approach, we characterized the dendritic morphology of cortical pyramidal neurons as well as the pattern of glutamatergic and GABAergic appositions on their cell bodies and dendrites. We focused on the association region of the parietal cortex (LtPA) and the medial prefrontal cortex (mPFC) for their involvement in the Morris water maze task. We found an age-related atrophy of distal basal dendrites that did not differ between aged cognitively unimpaired (AU) and aged cognitively impaired animals (AI). Dendritic spines and glutamatergic appositions generally decreased from young to AU and from AU to AI rats. On the other hand, GABAergic appositions only showed a trend towards a decrease in AU rats. Collectively, the data show that the ratio of excitatory/inhibitory inputs was only altered in AI animals. When cortical cholinergic varicosities were labeled on alternate sections, we found that AI animals also had a significant reduction of cortical cholinergic boutons compared with AU or young animals. In aged animals, the density of cortical cholinergic varicosities correlated with the excitatory/inhibitory ratio. Our data suggest that both cholinergic atrophy and an imbalance towards inhibition may contribute to the observed age-associated behavioral impairment.
众所周知,大脑皮层在衰老过程中会经历广泛的重塑。在这项研究中,我们使用经过行为特征描述的大鼠将与年龄相关的形态变化与认知障碍相关联。为此,年轻和老年动物在 Morris 水迷宫中接受测试,以评估它们的认知表现。在行为特征描述后,对动物进行灌注,并应用细胞内标记和免疫组织化学的组合。使用这种方法,我们描述了皮质锥体神经元的树突形态以及谷氨酸能和 GABA 能在其胞体和树突上的附着模式。我们专注于顶叶皮层(LtPA)和内侧前额叶皮层(mPFC)的关联区域,因为它们参与 Morris 水迷宫任务。我们发现与年龄相关的基底树突末梢萎缩,在认知未受损的老年动物(AU)和认知受损的老年动物(AI)之间没有差异。从年轻到 AU 再到 AI 大鼠,树突棘和谷氨酸能附着通常会减少。另一方面,GABA 能附着仅在 AU 大鼠中呈减少趋势。总的来说,数据表明兴奋性/抑制性输入的比例仅在 AI 动物中发生改变。当在交替切片上标记皮质胆碱能囊泡时,我们发现 AI 动物与 AU 或年轻动物相比,皮质胆碱能末梢也显著减少。在老年动物中,皮质胆碱能囊泡的密度与兴奋性/抑制性比值相关。我们的数据表明,胆碱能萎缩和抑制失衡都可能导致观察到的与年龄相关的行为障碍。