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Dissociable contributions of the medial parietal cortex to recognition memory

Human neuroimaging studies of episodic memory retrieval routinely observe the engagement of specific cortical regions beyond the medial temporal lobe. Of these, medial parietal cortex (MPC) is of particular interest given its ubiquitous, and yet distinct, functional characteristics during different...

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Detalles Bibliográficos
Autores principales: Koslov, Seth R., Kable, Joseph W., Foster, Brett L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515876/
https://www.ncbi.nlm.nih.gov/pubmed/37745317
http://dx.doi.org/10.1101/2023.09.12.557048
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author Koslov, Seth R.
Kable, Joseph W.
Foster, Brett L.
author_facet Koslov, Seth R.
Kable, Joseph W.
Foster, Brett L.
author_sort Koslov, Seth R.
collection PubMed
description Human neuroimaging studies of episodic memory retrieval routinely observe the engagement of specific cortical regions beyond the medial temporal lobe. Of these, medial parietal cortex (MPC) is of particular interest given its ubiquitous, and yet distinct, functional characteristics during different types of retrieval tasks. Specifically, while recognition memory and autobiographical recall tasks are both used to probe episodic retrieval, these paradigms consistently drive distinct patterns of response within MPC. This dissociation adds to growing evidence suggesting a common principle of functional organization across memory related brain structures, specifically regarding the control or content demands of memory-based decisions. To carefully examine this putative organization, we used a high-resolution fMRI dataset collected at ultra-high field (7T) while subjects performed thousands of recognition-memory trials to identify MPC regions responsive to recognition-decisions or semantic content of stimuli within and across individuals. We observed interleaving, though distinct, functional subregions of MPC where responses were sensitive to either recognition decisions or the semantic representation of stimuli, but rarely both. In addition, this functional dissociation within MPC was further accentuated by distinct profiles of connectivity bias with the hippocampus during task and rest. Finally, we show that recent observations of person and place selectivity within MPC reflect category specific responses from within identified semantic regions that are sensitive to mnemonic demands. Together, these data better account for how distinct patterns of MPC responses can occur as a result of task demands during episodic retrieval and may reflect a common principle of organization throughout hippocampal-neocortical memory systems.
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spelling pubmed-105158762023-09-23 Dissociable contributions of the medial parietal cortex to recognition memory Koslov, Seth R. Kable, Joseph W. Foster, Brett L. bioRxiv Article Human neuroimaging studies of episodic memory retrieval routinely observe the engagement of specific cortical regions beyond the medial temporal lobe. Of these, medial parietal cortex (MPC) is of particular interest given its ubiquitous, and yet distinct, functional characteristics during different types of retrieval tasks. Specifically, while recognition memory and autobiographical recall tasks are both used to probe episodic retrieval, these paradigms consistently drive distinct patterns of response within MPC. This dissociation adds to growing evidence suggesting a common principle of functional organization across memory related brain structures, specifically regarding the control or content demands of memory-based decisions. To carefully examine this putative organization, we used a high-resolution fMRI dataset collected at ultra-high field (7T) while subjects performed thousands of recognition-memory trials to identify MPC regions responsive to recognition-decisions or semantic content of stimuli within and across individuals. We observed interleaving, though distinct, functional subregions of MPC where responses were sensitive to either recognition decisions or the semantic representation of stimuli, but rarely both. In addition, this functional dissociation within MPC was further accentuated by distinct profiles of connectivity bias with the hippocampus during task and rest. Finally, we show that recent observations of person and place selectivity within MPC reflect category specific responses from within identified semantic regions that are sensitive to mnemonic demands. Together, these data better account for how distinct patterns of MPC responses can occur as a result of task demands during episodic retrieval and may reflect a common principle of organization throughout hippocampal-neocortical memory systems. Cold Spring Harbor Laboratory 2023-09-13 /pmc/articles/PMC10515876/ /pubmed/37745317 http://dx.doi.org/10.1101/2023.09.12.557048 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Koslov, Seth R.
Kable, Joseph W.
Foster, Brett L.
Dissociable contributions of the medial parietal cortex to recognition memory
title Dissociable contributions of the medial parietal cortex to recognition memory
title_full Dissociable contributions of the medial parietal cortex to recognition memory
title_fullStr Dissociable contributions of the medial parietal cortex to recognition memory
title_full_unstemmed Dissociable contributions of the medial parietal cortex to recognition memory
title_short Dissociable contributions of the medial parietal cortex to recognition memory
title_sort dissociable contributions of the medial parietal cortex to recognition memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515876/
https://www.ncbi.nlm.nih.gov/pubmed/37745317
http://dx.doi.org/10.1101/2023.09.12.557048
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