High-Fidelity Mapping of Repetition-Related Changes in the Parietal Memory Network

item.page.doi

Abstract

fMRI studies of human memory have identified a “parietal memory network” (PMN) that displays distinct responses to novel and familiar stimuli, typically deactivating during initial encoding but robustly activating during retrieval. The small size of PMN regions, combined with their proximity to the neighboring default mode network, makes a targeted assessment of their responses in highly sampled subjects important for understanding information processing within the network. Here, we describe an experiment in which participants made semantic decisions about repeatedly-presented stimuli, assessing PMN BOLD responses as items transitioned from experimentally novel to repeated. Data are from the highly-sampled subjects in the Midnight Scan Club dataset, enabling a characterization of BOLD responses at both the group and single-subject level. Across all analyses, PMN regions deactivated in response to novel stimuli and displayed changes in BOLD activity across presentations, but did not significantly activate to repeated items. Results support only a portion of initially hypothesized effects, in particular suggesting that novelty-related deactivations may be less susceptible to attentional/task manipulations than are repetition-related activations within the network. This in turn suggests that novelty and familiarity may be processed as separable entities within the PMN. © 2019 The Authors

Description

Supplementary material is available on publisher's website. Use the DOI link below.
Due to copyright restrictions and/or publisher's policy full text access from Treasures at UT Dallas is limited to current UTD affiliates (use the provided Link to Article).

Keywords

Magnetic resonance imaging, Highly-sampled human subjects, Magnetic resonance imaging, Information retrieval

item.page.sponsorship

National Science Foundation Graduate Research Fellowship DGE-1143954; National Institutes of Health Grants NS088590, TR000448, MH104592, 1R25MH112473, 1P30NS098577, and HD087011

Rights

©2019 The Authors

Citation

Collections