TY - JOUR
AU - Stangl, Matthias
AU - Achtzehn, Johannes
AU - Huber, Karin
AU - Dietrich, Caroline
AU - Tempelmann, Claus
AU - Wolbers, Thomas
TI - Compromised Grid-Cell-like Representations in Old Age as a Key Mechanism to Explain Age-Related Navigational Deficits.
JO - Current biology
VL - 28
IS - 7
SN - 0960-9822
CY - London
PB - Current Biology Ltd.
M1 - DZNE-2020-06209
SP - 1108-1115.e6
PY - 2018
AB - 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.
KW - Adult
KW - Aged
KW - Aging: pathology
KW - Cognition: physiology
KW - Entorhinal Cortex: physiology
KW - Female
KW - Grid Cells: physiology
KW - Humans
KW - Male
KW - Spatial Memory: physiology
KW - Spatial Navigation: physiology
LB - PUB:(DE-HGF)16
C6 - pmid:29551413
C2 - pmc:PMC5887108
DO - DOI:10.1016/j.cub.2018.02.038
UR - https://pub.dzne.de/record/139887
ER -