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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-9667293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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