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Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation

The hippocampus has been a focus of memory research since H.M’s surgery abolished his ability to form new memories, yet its mechanistic role in memory remains debated. Here, we identify a candidate memory mechanism: an anticipatory hippocampal “convergence state”, observed while awaiting valuable in...

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Autores principales: Poh, Jia-Hou, Vu, Mai-Anh T., Stanek, Jessica K., Hsiung, Abigail, Egner, Tobias, Adcock, R. Alison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640528/
https://www.ncbi.nlm.nih.gov/pubmed/36344524
http://dx.doi.org/10.1038/s41467-022-34459-3
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author Poh, Jia-Hou
Vu, Mai-Anh T.
Stanek, Jessica K.
Hsiung, Abigail
Egner, Tobias
Adcock, R. Alison
author_facet Poh, Jia-Hou
Vu, Mai-Anh T.
Stanek, Jessica K.
Hsiung, Abigail
Egner, Tobias
Adcock, R. Alison
author_sort Poh, Jia-Hou
collection PubMed
description The hippocampus has been a focus of memory research since H.M’s surgery abolished his ability to form new memories, yet its mechanistic role in memory remains debated. Here, we identify a candidate memory mechanism: an anticipatory hippocampal “convergence state”, observed while awaiting valuable information, and which predicts subsequent learning. During fMRI, participants viewed trivia questions eliciting high or low curiosity, followed seconds later by its answer. We reasoned that encoding success requires a confluence of conditions, so that hippocampal states more conducive to memory formation should converge in state space. To operationalize convergence of neural states, we quantified the typicality of multivoxel patterns in the medial temporal lobes during anticipation and encoding of trivia answers. We found that the typicality of anticipatory hippocampal patterns increased during high curiosity. Crucially, anticipatory hippocampal pattern typicality increased with dopaminergic midbrain activation and uniquely accounted for the association between midbrain activation and subsequent recall. We propose that hippocampal convergence states may complete a cascade from motivation and midbrain activation to memory enhancement, and may be a general predictor of memory formation.
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spelling pubmed-96405282022-11-15 Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation Poh, Jia-Hou Vu, Mai-Anh T. Stanek, Jessica K. Hsiung, Abigail Egner, Tobias Adcock, R. Alison Nat Commun Article The hippocampus has been a focus of memory research since H.M’s surgery abolished his ability to form new memories, yet its mechanistic role in memory remains debated. Here, we identify a candidate memory mechanism: an anticipatory hippocampal “convergence state”, observed while awaiting valuable information, and which predicts subsequent learning. During fMRI, participants viewed trivia questions eliciting high or low curiosity, followed seconds later by its answer. We reasoned that encoding success requires a confluence of conditions, so that hippocampal states more conducive to memory formation should converge in state space. To operationalize convergence of neural states, we quantified the typicality of multivoxel patterns in the medial temporal lobes during anticipation and encoding of trivia answers. We found that the typicality of anticipatory hippocampal patterns increased during high curiosity. Crucially, anticipatory hippocampal pattern typicality increased with dopaminergic midbrain activation and uniquely accounted for the association between midbrain activation and subsequent recall. We propose that hippocampal convergence states may complete a cascade from motivation and midbrain activation to memory enhancement, and may be a general predictor of memory formation. Nature Publishing Group UK 2022-11-07 /pmc/articles/PMC9640528/ /pubmed/36344524 http://dx.doi.org/10.1038/s41467-022-34459-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Poh, Jia-Hou
Vu, Mai-Anh T.
Stanek, Jessica K.
Hsiung, Abigail
Egner, Tobias
Adcock, R. Alison
Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title_full Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title_fullStr Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title_full_unstemmed Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title_short Hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
title_sort hippocampal convergence during anticipatory midbrain activation promotes subsequent memory formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640528/
https://www.ncbi.nlm.nih.gov/pubmed/36344524
http://dx.doi.org/10.1038/s41467-022-34459-3
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