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vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness

Our ability to recall past experiences, autobiographical memories (AMs), is crucial to cognition, endowing us with a sense of self and underwriting our capacity for autonomy. Traditional views assume that the hippocampus orchestrates event recall, whereas recent accounts propose that the ventromedia...

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Autores principales: McCormick, Cornelia, Barry, Daniel N, Jafarian, Amirhossein, Barnes, Gareth R, Maguire, Eleanor A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899055/
https://www.ncbi.nlm.nih.gov/pubmed/32572443
http://dx.doi.org/10.1093/cercor/bhaa172
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author McCormick, Cornelia
Barry, Daniel N
Jafarian, Amirhossein
Barnes, Gareth R
Maguire, Eleanor A
author_facet McCormick, Cornelia
Barry, Daniel N
Jafarian, Amirhossein
Barnes, Gareth R
Maguire, Eleanor A
author_sort McCormick, Cornelia
collection PubMed
description Our ability to recall past experiences, autobiographical memories (AMs), is crucial to cognition, endowing us with a sense of self and underwriting our capacity for autonomy. Traditional views assume that the hippocampus orchestrates event recall, whereas recent accounts propose that the ventromedial prefrontal cortex (vmPFC) instigates and coordinates hippocampal-dependent processes. Here we sought to characterize the dynamic interplay between the hippocampus and vmPFC during AM recall to adjudicate between these perspectives. Leveraging the high temporal resolution of magnetoencephalography, we found that the left hippocampus and the vmPFC showed the greatest power changes during AM retrieval. Moreover, responses in the vmPFC preceded activity in the hippocampus during initiation of AM recall, except during retrieval of the most recent AMs. The vmPFC drove hippocampal activity during recall initiation and also as AMs unfolded over subsequent seconds, and this effect was evident regardless of AM age. These results recast the positions of the hippocampus and the vmPFC in the AM retrieval hierarchy, with implications for theoretical accounts of memory processing and systems-level consolidation.
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spelling pubmed-78990552021-02-25 vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness McCormick, Cornelia Barry, Daniel N Jafarian, Amirhossein Barnes, Gareth R Maguire, Eleanor A Cereb Cortex Original Article Our ability to recall past experiences, autobiographical memories (AMs), is crucial to cognition, endowing us with a sense of self and underwriting our capacity for autonomy. Traditional views assume that the hippocampus orchestrates event recall, whereas recent accounts propose that the ventromedial prefrontal cortex (vmPFC) instigates and coordinates hippocampal-dependent processes. Here we sought to characterize the dynamic interplay between the hippocampus and vmPFC during AM recall to adjudicate between these perspectives. Leveraging the high temporal resolution of magnetoencephalography, we found that the left hippocampus and the vmPFC showed the greatest power changes during AM retrieval. Moreover, responses in the vmPFC preceded activity in the hippocampus during initiation of AM recall, except during retrieval of the most recent AMs. The vmPFC drove hippocampal activity during recall initiation and also as AMs unfolded over subsequent seconds, and this effect was evident regardless of AM age. These results recast the positions of the hippocampus and the vmPFC in the AM retrieval hierarchy, with implications for theoretical accounts of memory processing and systems-level consolidation. Oxford University Press 2020-06-23 /pmc/articles/PMC7899055/ /pubmed/32572443 http://dx.doi.org/10.1093/cercor/bhaa172 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
McCormick, Cornelia
Barry, Daniel N
Jafarian, Amirhossein
Barnes, Gareth R
Maguire, Eleanor A
vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title_full vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title_fullStr vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title_full_unstemmed vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title_short vmPFC Drives Hippocampal Processing during Autobiographical Memory Recall Regardless of Remoteness
title_sort vmpfc drives hippocampal processing during autobiographical memory recall regardless of remoteness
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899055/
https://www.ncbi.nlm.nih.gov/pubmed/32572443
http://dx.doi.org/10.1093/cercor/bhaa172
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