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Stability of ripple events during task engagement in human hippocampus

High-frequency activity bursts in the hippocampus, known as ripples, are thought to support memory consolidation during “offline” states, such as sleep. Recently, human hippocampal ripples have been observed during “online” episodic memory tasks. It remains unclear whether similar ripple activity oc...

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Autores principales: Chen, Yvonne Y., Aponik-Gremillion, Lyndsey, Bartoli, Eleonora, Yoshor, Daniel, Sheth, Sameer A., Foster, Brett L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288441/
https://www.ncbi.nlm.nih.gov/pubmed/34192546
http://dx.doi.org/10.1016/j.celrep.2021.109304
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author Chen, Yvonne Y.
Aponik-Gremillion, Lyndsey
Bartoli, Eleonora
Yoshor, Daniel
Sheth, Sameer A.
Foster, Brett L.
author_facet Chen, Yvonne Y.
Aponik-Gremillion, Lyndsey
Bartoli, Eleonora
Yoshor, Daniel
Sheth, Sameer A.
Foster, Brett L.
author_sort Chen, Yvonne Y.
collection PubMed
description High-frequency activity bursts in the hippocampus, known as ripples, are thought to support memory consolidation during “offline” states, such as sleep. Recently, human hippocampal ripples have been observed during “online” episodic memory tasks. It remains unclear whether similar ripple activity occurs during other cognitive states, including different types of episodic memory. However, identifying genuine ripple events in the human hippocampus is challenging. To address these questions, spectro-temporal ripple identification was applied to human hippocampal recordings across a variety of cognitive tasks. Overall, ripple attributes were stable across tasks of visual perception and associative memory, with mean rates lower than offline states of rest and sleep. In contrast, while more complex visual attention tasks did not modulate ripple attributes, rates were enhanced for more complex autobiographical memory conditions. Therefore, hippocampal ripples reliably occur across cognitive states but are specifically enhanced during offline states and complex memory processes, consistent with a role in consolidation.
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spelling pubmed-82884412021-07-19 Stability of ripple events during task engagement in human hippocampus Chen, Yvonne Y. Aponik-Gremillion, Lyndsey Bartoli, Eleonora Yoshor, Daniel Sheth, Sameer A. Foster, Brett L. Cell Rep Article High-frequency activity bursts in the hippocampus, known as ripples, are thought to support memory consolidation during “offline” states, such as sleep. Recently, human hippocampal ripples have been observed during “online” episodic memory tasks. It remains unclear whether similar ripple activity occurs during other cognitive states, including different types of episodic memory. However, identifying genuine ripple events in the human hippocampus is challenging. To address these questions, spectro-temporal ripple identification was applied to human hippocampal recordings across a variety of cognitive tasks. Overall, ripple attributes were stable across tasks of visual perception and associative memory, with mean rates lower than offline states of rest and sleep. In contrast, while more complex visual attention tasks did not modulate ripple attributes, rates were enhanced for more complex autobiographical memory conditions. Therefore, hippocampal ripples reliably occur across cognitive states but are specifically enhanced during offline states and complex memory processes, consistent with a role in consolidation. 2021-06-29 /pmc/articles/PMC8288441/ /pubmed/34192546 http://dx.doi.org/10.1016/j.celrep.2021.109304 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Chen, Yvonne Y.
Aponik-Gremillion, Lyndsey
Bartoli, Eleonora
Yoshor, Daniel
Sheth, Sameer A.
Foster, Brett L.
Stability of ripple events during task engagement in human hippocampus
title Stability of ripple events during task engagement in human hippocampus
title_full Stability of ripple events during task engagement in human hippocampus
title_fullStr Stability of ripple events during task engagement in human hippocampus
title_full_unstemmed Stability of ripple events during task engagement in human hippocampus
title_short Stability of ripple events during task engagement in human hippocampus
title_sort stability of ripple events during task engagement in human hippocampus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288441/
https://www.ncbi.nlm.nih.gov/pubmed/34192546
http://dx.doi.org/10.1016/j.celrep.2021.109304
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