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Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning
The hippocampus is crucial for episodic or declarative memory and the theta rhythm has been implicated in mnemonic processing, but the functional contribution of theta to memory remains the subject of intense speculation. Recent evidence suggests that the hippocampus might function as a network hub...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289589/ https://www.ncbi.nlm.nih.gov/pubmed/22389627 http://dx.doi.org/10.1371/journal.pbio.1001267 |
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author | Kaplan, Raphael Doeller, Christian F. Barnes, Gareth R. Litvak, Vladimir Düzel, Emrah Bandettini, Peter A. Burgess, Neil |
author_facet | Kaplan, Raphael Doeller, Christian F. Barnes, Gareth R. Litvak, Vladimir Düzel, Emrah Bandettini, Peter A. Burgess, Neil |
author_sort | Kaplan, Raphael |
collection | PubMed |
description | The hippocampus is crucial for episodic or declarative memory and the theta rhythm has been implicated in mnemonic processing, but the functional contribution of theta to memory remains the subject of intense speculation. Recent evidence suggests that the hippocampus might function as a network hub for volitional learning. In contrast to human experiments, electrophysiological recordings in the hippocampus of behaving rodents are dominated by theta oscillations reflecting volitional movement, which has been linked to spatial exploration and encoding. This literature makes the surprising cross-species prediction that the human hippocampal theta rhythm supports memory by coordinating exploratory movements in the service of self-directed learning. We examined the links between theta, spatial exploration, and memory encoding by designing an interactive human spatial navigation paradigm combined with multimodal neuroimaging. We used both non-invasive whole-head Magnetoencephalography (MEG) to look at theta oscillations and Functional Magnetic Resonance Imaging (fMRI) to look at brain regions associated with volitional movement and learning. We found that theta power increases during the self-initiation of virtual movement, additionally correlating with subsequent memory performance and environmental familiarity. Performance-related hippocampal theta increases were observed during a static pre-navigation retrieval phase, where planning for subsequent navigation occurred. Furthermore, periods of the task showing movement-related theta increases showed decreased fMRI activity in the parahippocampus and increased activity in the hippocampus and other brain regions that strikingly overlap with the previously observed volitional learning network (the reverse pattern was seen for stationary periods). These fMRI changes also correlated with participant's performance. Our findings suggest that the human hippocampal theta rhythm supports memory by coordinating exploratory movements in the service of self-directed learning. These findings directly extend the role of the hippocampus in spatial exploration in rodents to human memory and self-directed learning. |
format | Online Article Text |
id | pubmed-3289589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32895892012-03-02 Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning Kaplan, Raphael Doeller, Christian F. Barnes, Gareth R. Litvak, Vladimir Düzel, Emrah Bandettini, Peter A. Burgess, Neil PLoS Biol Research Article The hippocampus is crucial for episodic or declarative memory and the theta rhythm has been implicated in mnemonic processing, but the functional contribution of theta to memory remains the subject of intense speculation. Recent evidence suggests that the hippocampus might function as a network hub for volitional learning. In contrast to human experiments, electrophysiological recordings in the hippocampus of behaving rodents are dominated by theta oscillations reflecting volitional movement, which has been linked to spatial exploration and encoding. This literature makes the surprising cross-species prediction that the human hippocampal theta rhythm supports memory by coordinating exploratory movements in the service of self-directed learning. We examined the links between theta, spatial exploration, and memory encoding by designing an interactive human spatial navigation paradigm combined with multimodal neuroimaging. We used both non-invasive whole-head Magnetoencephalography (MEG) to look at theta oscillations and Functional Magnetic Resonance Imaging (fMRI) to look at brain regions associated with volitional movement and learning. We found that theta power increases during the self-initiation of virtual movement, additionally correlating with subsequent memory performance and environmental familiarity. Performance-related hippocampal theta increases were observed during a static pre-navigation retrieval phase, where planning for subsequent navigation occurred. Furthermore, periods of the task showing movement-related theta increases showed decreased fMRI activity in the parahippocampus and increased activity in the hippocampus and other brain regions that strikingly overlap with the previously observed volitional learning network (the reverse pattern was seen for stationary periods). These fMRI changes also correlated with participant's performance. Our findings suggest that the human hippocampal theta rhythm supports memory by coordinating exploratory movements in the service of self-directed learning. These findings directly extend the role of the hippocampus in spatial exploration in rodents to human memory and self-directed learning. Public Library of Science 2012-02-28 /pmc/articles/PMC3289589/ /pubmed/22389627 http://dx.doi.org/10.1371/journal.pbio.1001267 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Kaplan, Raphael Doeller, Christian F. Barnes, Gareth R. Litvak, Vladimir Düzel, Emrah Bandettini, Peter A. Burgess, Neil Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title | Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title_full | Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title_fullStr | Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title_full_unstemmed | Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title_short | Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning |
title_sort | movement-related theta rhythm in humans: coordinating self-directed hippocampal learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289589/ https://www.ncbi.nlm.nih.gov/pubmed/22389627 http://dx.doi.org/10.1371/journal.pbio.1001267 |
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