Smith David E, Rapp Peter R, McKay Heather M, Roberts Jeffrey A, Tuszynski Mark H
Department of Neurosciences, University of California, San Diego, La Jolla, California 92093-0626, USA.
J Neurosci. 2004 May 5;24(18):4373-81. doi: 10.1523/JNEUROSCI.4289-03.2004.
Mechanisms of cognitive decline with aging remain primarily unknown. We determined whether localized cell loss occurred in brain regions associated with age-related cognitive decline in primates. On a task requiring the prefrontal cortex, aged monkeys were impaired in maintaining representations in working memory. Stereological quantification in area 8A, a prefrontal region associated with working memory, demonstrated a significant 32 +/- 11% reduction in the number of Nissl-stained neurons compared with young monkeys. Furthermore, the number of immunolabeled cholinergic neurons projecting to this region of cortex from the nucleus basalis was also reduced by 50 +/- 6%. In contrast, neuronal number was strikingly preserved in an adjoining prefrontal cortical region also associated with working memory, area 46, and in the component of the nucleus basalis projecting to this region. These findings demonstrate extensive but highly localized loss of neocortical neurons in aged, cognitively impaired monkeys that likely contributes to cognitive decline. Cell degeneration, when present, extends transneuronally.
衰老导致认知衰退的机制基本上仍不为人知。我们确定了在与灵长类动物年龄相关的认知衰退相关的脑区中是否发生了局部细胞丢失。在一项需要前额叶皮层参与的任务中,老年猴子在工作记忆中维持表象的能力受损。在与工作记忆相关的前额叶区域8A进行的体视学定量分析表明,与年轻猴子相比,尼氏染色神经元数量显著减少了32±11%。此外,从基底核投射到该皮层区域的免疫标记胆碱能神经元数量也减少了50±6%。相比之下,在同样与工作记忆相关的相邻前额叶皮层区域46以及投射到该区域的基底核部分,神经元数量显著保留。这些发现表明,在认知受损的老年猴子中,新皮层神经元存在广泛但高度局部化的丢失,这可能导致认知衰退。当出现细胞变性时,它会跨神经元扩展。