Objectives: Cognitive flexibility declines with aging and is usually indicated by task switch costs including global and local switch costs. Cognitive flexibility in aging is associated with alterations in functional connectivity. However, whether different task-modulated connectivity mechanisms underlying global and local switch costs remain unclear.
Methods: Here we use the support vector machine to identify age-related functional connectivity in global and local switch costs between older (n = 32) and young adults (n = 33). Participants completed a cued task-switching task during the functional magnetic resonance imaging scan.
Results: Results show an age-related decline behaviorally in global but not in local switch costs. Moreover, distinct patterns of age-related alterations of connectivity were observed for each cost. Specifically, only multivariate changes in connectivity patterns were observed for local switch cost, whereas specific age-related connections were revealed for global switch cost. In older adults, the task-modulated left dorsal premotor cortex-left precuneus connectivity decreased, and the left inferior frontal junction-left inferior parietal sulcus connectivity correlated with decreased global switch cost.
Discussion: This study provides novel evidence for different neural patterns in global and local switch costs by illuminating connectivity mechanisms underlying cognitive flexibility in aging.
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http://dx.doi.org/10.1093/geronb/gbad092 | DOI Listing |
We develop fs laser-fabricated asymmetric couplers and zig-zag arrays consisting of single- and two-mode waveguides with bipartite Kerr nonlinearity in borosilicate (BK7) glass substrates. The fundamental mode ( orbital) is near resonance with the neighboring higher-order orbital, causing efficient light transfer at low power. Due to Kerr nonlinearity, the coupler works as an all-optical switch between and orbitals.
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The regulation of cellular metabolism is crucial for cell survival, with Sch9 in serving a key role as a substrate of TORC1. Sch9 localizes to the vacuolar membrane through binding to PI(3,5)P, which is necessary for TORC1-dependent phosphorylation. This study demonstrates that cytosolic pH regulates Sch9 localization.
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