German Center for Neurodegenerative Diseases (DZNE), Aging & Cognition Research Group, Leipziger Str. 44, 39120 Magdeburg, Germany.
German Center for Neurodegenerative Diseases (DZNE), Aging & Cognition Research Group, Leipziger Str. 44, 39120 Magdeburg, Germany.
Curr Biol. 2018 Apr 2;28(7):1108-1115.e6. doi: 10.1016/j.cub.2018.02.038. Epub 2018 Mar 15.
A progressive loss of navigational abilities in old age has been observed in numerous studies, but we have only limited understanding of the neural mechanisms underlying this decline [1]. A central component of the brain's navigation circuit are grid cells in entorhinal cortex [2], largely thought to support intrinsic self-motion-related computations, such as path integration (i.e., keeping track of one's position by integrating self-motion cues) [3-6]. Given that entorhinal cortex is particularly vulnerable to neurodegenerative processes during aging and Alzheimer's disease [7-14], deficits in grid cell function could be a key mechanism to explain age-related navigational decline. To test this hypothesis, we conducted two experiments in healthy young and older adults. First, in an fMRI experiment, we found significantly reduced grid-cell-like representations in entorhinal cortex of older adults. Second, in a behavioral path integration experiment, older adults showed deficits in computations of self-position during path integration based on body-based or visual self-motion cues. Most strikingly, we found that these path integration deficits in older adults could be explained by their individual magnitudes of grid-cell-like representations, as reduced grid-cell-like representations were associated with larger path integration errors. Together, these results show that grid-cell-like representations in entorhinal cortex are compromised in healthy aging. Furthermore, the association between grid-cell-like representations and path integration performance in old age supports the notion that grid cells underlie path integration processes. We therefore conclude that impaired grid cell function may play a key role in age-related decline of specific higher-order cognitive functions, such as spatial navigation.
许多研究都观察到老年人在导航能力上的逐渐丧失,但我们对这种衰退的神经机制只有有限的了解[1]。大脑导航回路的一个核心组成部分是内嗅皮层中的网格细胞[2],这些细胞被认为主要支持内在的自我运动相关计算,如路径整合(即通过整合自我运动线索来跟踪自己的位置)[3-6]。鉴于内嗅皮层在衰老和阿尔茨海默病期间特别容易受到神经退行性过程的影响[7-14],网格细胞功能的缺陷可能是解释与年龄相关的导航衰退的关键机制。为了验证这一假设,我们在健康的年轻和老年成年人中进行了两项实验。首先,在 fMRI 实验中,我们发现老年人大脑中内嗅皮层的网格细胞样表示显著减少。其次,在行为路径整合实验中,老年人在基于身体或视觉自我运动线索的路径整合中表现出自定位计算的缺陷。最引人注目的是,我们发现老年人大脑中的这些路径整合缺陷可以用他们个体的网格细胞样表示来解释,因为减少的网格细胞样表示与更大的路径整合错误相关。总的来说,这些结果表明,内嗅皮层中的网格细胞样表示在健康衰老中受到了损害。此外,老年人大脑中网格细胞样表示与路径整合表现之间的关联支持了网格细胞是路径整合过程基础的观点。因此,我们得出结论,网格细胞功能的受损可能在特定高级认知功能(如空间导航)的与年龄相关的衰退中起着关键作用。