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Running speed and REM sleep control two distinct modes of rapid interhemispheric communication
Rhythmic gamma-band communication within and across cortical hemispheres is critical for optimal perception, navigation, and memory. Here, using multisite recordings in both rats and mice, we show that even faster ~140 Hz rhythms are robustly anti-phase across cortical hemispheres, visually resembli...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291430/ https://www.ncbi.nlm.nih.gov/pubmed/35793619 http://dx.doi.org/10.1016/j.celrep.2022.111028 |
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author | Ghosh, Megha Yang, Fang-Chi Rice, Sharena P. Hetrick, Vaughn Gonzalez, Alcides Lorenzo Siu, Danny Brennan, Ellen K.W. John, Tibin T. Ahrens, Allison M. Ahmed, Omar J. |
author_facet | Ghosh, Megha Yang, Fang-Chi Rice, Sharena P. Hetrick, Vaughn Gonzalez, Alcides Lorenzo Siu, Danny Brennan, Ellen K.W. John, Tibin T. Ahrens, Allison M. Ahmed, Omar J. |
author_sort | Ghosh, Megha |
collection | PubMed |
description | Rhythmic gamma-band communication within and across cortical hemispheres is critical for optimal perception, navigation, and memory. Here, using multisite recordings in both rats and mice, we show that even faster ~140 Hz rhythms are robustly anti-phase across cortical hemispheres, visually resembling splines, the interlocking teeth on mechanical gears. Splines are strongest in superficial granular retrosplenial cortex, a region important for spatial navigation and memory. Spline-frequency interhemispheric communication becomes more coherent and more precisely anti-phase at faster running speeds. Anti-phase splines also demarcate high-activity frames during REM sleep. While splines and associated neuronal spiking are anti-phase across retrosplenial hemispheres during navigation and REM sleep, gamma-rhythmic interhemispheric communication is precisely in-phase. Gamma and splines occur at distinct points of a theta cycle and thus highlight the ability of interhemispheric cortical communication to rapidly switch between in-phase (gamma) and anti-phase (spline) modes within individual theta cycles during both navigation and REM sleep. |
format | Online Article Text |
id | pubmed-9291430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-92914302022-07-18 Running speed and REM sleep control two distinct modes of rapid interhemispheric communication Ghosh, Megha Yang, Fang-Chi Rice, Sharena P. Hetrick, Vaughn Gonzalez, Alcides Lorenzo Siu, Danny Brennan, Ellen K.W. John, Tibin T. Ahrens, Allison M. Ahmed, Omar J. Cell Rep Article Rhythmic gamma-band communication within and across cortical hemispheres is critical for optimal perception, navigation, and memory. Here, using multisite recordings in both rats and mice, we show that even faster ~140 Hz rhythms are robustly anti-phase across cortical hemispheres, visually resembling splines, the interlocking teeth on mechanical gears. Splines are strongest in superficial granular retrosplenial cortex, a region important for spatial navigation and memory. Spline-frequency interhemispheric communication becomes more coherent and more precisely anti-phase at faster running speeds. Anti-phase splines also demarcate high-activity frames during REM sleep. While splines and associated neuronal spiking are anti-phase across retrosplenial hemispheres during navigation and REM sleep, gamma-rhythmic interhemispheric communication is precisely in-phase. Gamma and splines occur at distinct points of a theta cycle and thus highlight the ability of interhemispheric cortical communication to rapidly switch between in-phase (gamma) and anti-phase (spline) modes within individual theta cycles during both navigation and REM sleep. 2022-07-05 /pmc/articles/PMC9291430/ /pubmed/35793619 http://dx.doi.org/10.1016/j.celrep.2022.111028 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 Ghosh, Megha Yang, Fang-Chi Rice, Sharena P. Hetrick, Vaughn Gonzalez, Alcides Lorenzo Siu, Danny Brennan, Ellen K.W. John, Tibin T. Ahrens, Allison M. Ahmed, Omar J. Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title | Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title_full | Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title_fullStr | Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title_full_unstemmed | Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title_short | Running speed and REM sleep control two distinct modes of rapid interhemispheric communication |
title_sort | running speed and rem sleep control two distinct modes of rapid interhemispheric communication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291430/ https://www.ncbi.nlm.nih.gov/pubmed/35793619 http://dx.doi.org/10.1016/j.celrep.2022.111028 |
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