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Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats

Hippocampal theta and gamma rhythms are hypothesized to play a role in the physiology of higher cognition. Prior research has reported that an offset in theta cycles between the entorhinal cortex, CA3, and CA1 regions promotes independence of population activity across the hippocampus. In line with...

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Detalles Bibliográficos
Autores principales: Zhou, Yuchen, Sheremet, Alex, Kennedy, Jack P., Qin, Yu, DiCola, Nicholas M., Lovett, Sarah D., Burke, Sara N., Maurer, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667293/
https://www.ncbi.nlm.nih.gov/pubmed/36405771
http://dx.doi.org/10.1016/j.isci.2022.105457
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author Zhou, Yuchen
Sheremet, Alex
Kennedy, Jack P.
Qin, Yu
DiCola, Nicholas M.
Lovett, Sarah D.
Burke, Sara N.
Maurer, Andrew P.
author_facet Zhou, Yuchen
Sheremet, Alex
Kennedy, Jack P.
Qin, Yu
DiCola, Nicholas M.
Lovett, Sarah D.
Burke, Sara N.
Maurer, Andrew P.
author_sort Zhou, Yuchen
collection PubMed
description Hippocampal theta and gamma rhythms are hypothesized to play a role in the physiology of higher cognition. Prior research has reported that an offset in theta cycles between the entorhinal cortex, CA3, and CA1 regions promotes independence of population activity across the hippocampus. In line with this idea, it has recently been observed that CA1 pyramidal cells can establish and maintain coordinated place cell activity intrinsically, with minimal reliance on afferent input. Counter to these observations is the contemporary hypothesis that CA1 neuron activity is driven by a gamma oscillation arising from the medial entorhinal cortex (MEC) that relays information by providing precisely timed synchrony between MEC and CA1. Reinvestigating this in rats during appetitive track running, we found that theta is the dominant frequency of cross-frequency coupling between the MEC and hippocampus, with hippocampal gamma largely independent of entorhinal gamma.
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spelling pubmed-96672932022-11-17 Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats Zhou, Yuchen Sheremet, Alex Kennedy, Jack P. Qin, Yu DiCola, Nicholas M. Lovett, Sarah D. Burke, Sara N. Maurer, Andrew P. iScience Article Hippocampal theta and gamma rhythms are hypothesized to play a role in the physiology of higher cognition. Prior research has reported that an offset in theta cycles between the entorhinal cortex, CA3, and CA1 regions promotes independence of population activity across the hippocampus. In line with this idea, it has recently been observed that CA1 pyramidal cells can establish and maintain coordinated place cell activity intrinsically, with minimal reliance on afferent input. Counter to these observations is the contemporary hypothesis that CA1 neuron activity is driven by a gamma oscillation arising from the medial entorhinal cortex (MEC) that relays information by providing precisely timed synchrony between MEC and CA1. Reinvestigating this in rats during appetitive track running, we found that theta is the dominant frequency of cross-frequency coupling between the MEC and hippocampus, with hippocampal gamma largely independent of entorhinal gamma. Elsevier 2022-10-29 /pmc/articles/PMC9667293/ /pubmed/36405771 http://dx.doi.org/10.1016/j.isci.2022.105457 Text en © 2022 The Author(s) 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/).
spellingShingle Article
Zhou, Yuchen
Sheremet, Alex
Kennedy, Jack P.
Qin, Yu
DiCola, Nicholas M.
Lovett, Sarah D.
Burke, Sara N.
Maurer, Andrew P.
Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title_full Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title_fullStr Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title_full_unstemmed Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title_short Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
title_sort theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667293/
https://www.ncbi.nlm.nih.gov/pubmed/36405771
http://dx.doi.org/10.1016/j.isci.2022.105457
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