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Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation
Interhemispheric correlation between homotopic areas is a major hallmark of cortical physiology and is believed to emerge through the corpus callosum. However, how interhemispheric correlations and corpus callosum activity are affected by behavioral states remains unknown. We performed laminar extra...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253780/ https://www.ncbi.nlm.nih.gov/pubmed/34215734 http://dx.doi.org/10.1038/s41467-021-24310-6 |
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author | Oran, Yael Katz, Yonatan Sokoletsky, Michael Malina, Katayun Cohen-Kashi Lampl, Ilan |
author_facet | Oran, Yael Katz, Yonatan Sokoletsky, Michael Malina, Katayun Cohen-Kashi Lampl, Ilan |
author_sort | Oran, Yael |
collection | PubMed |
description | Interhemispheric correlation between homotopic areas is a major hallmark of cortical physiology and is believed to emerge through the corpus callosum. However, how interhemispheric correlations and corpus callosum activity are affected by behavioral states remains unknown. We performed laminar extracellular and intracellular recordings simultaneously from both barrel cortices in awake mice. We find robust interhemispheric correlations of both spiking and synaptic activities that are reduced during whisking compared to quiet wakefulness. Accordingly, optogenetic inactivation of one hemisphere reveals that interhemispheric coupling occurs only during quiet wakefulness, and chemogenetic inactivation of callosal terminals reduces interhemispheric correlation especially during quiet wakefulness. Moreover, in contrast to the generally elevated firing rate observed during whisking epochs, we find a marked decrease in the activity of imaged callosal fibers. Our results indicate that the reduction in interhemispheric coupling and correlations during active behavior reflects the specific reduction in the activity of callosal neurons. |
format | Online Article Text |
id | pubmed-8253780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82537802021-07-20 Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation Oran, Yael Katz, Yonatan Sokoletsky, Michael Malina, Katayun Cohen-Kashi Lampl, Ilan Nat Commun Article Interhemispheric correlation between homotopic areas is a major hallmark of cortical physiology and is believed to emerge through the corpus callosum. However, how interhemispheric correlations and corpus callosum activity are affected by behavioral states remains unknown. We performed laminar extracellular and intracellular recordings simultaneously from both barrel cortices in awake mice. We find robust interhemispheric correlations of both spiking and synaptic activities that are reduced during whisking compared to quiet wakefulness. Accordingly, optogenetic inactivation of one hemisphere reveals that interhemispheric coupling occurs only during quiet wakefulness, and chemogenetic inactivation of callosal terminals reduces interhemispheric correlation especially during quiet wakefulness. Moreover, in contrast to the generally elevated firing rate observed during whisking epochs, we find a marked decrease in the activity of imaged callosal fibers. Our results indicate that the reduction in interhemispheric coupling and correlations during active behavior reflects the specific reduction in the activity of callosal neurons. Nature Publishing Group UK 2021-07-02 /pmc/articles/PMC8253780/ /pubmed/34215734 http://dx.doi.org/10.1038/s41467-021-24310-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oran, Yael Katz, Yonatan Sokoletsky, Michael Malina, Katayun Cohen-Kashi Lampl, Ilan Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title | Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title_full | Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title_fullStr | Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title_full_unstemmed | Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title_short | Reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
title_sort | reduction of corpus callosum activity during whisking leads to interhemispheric decorrelation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253780/ https://www.ncbi.nlm.nih.gov/pubmed/34215734 http://dx.doi.org/10.1038/s41467-021-24310-6 |
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