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Structure of cortical network activity across natural wake and sleep states in mice
Cortical neurons fire intermittently and synchronously during non-rapid eye movement sleep (NREMS), in which active and silent periods are referred to as ON and OFF periods, respectively. Neuronal firing rates during ON periods (NREMS-ON-activity) are similar to those of wakefulness (W-activity), ra...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259746/ https://www.ncbi.nlm.nih.gov/pubmed/32470016 http://dx.doi.org/10.1371/journal.pone.0233561 |
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author | Ohyama, Kaoru Kanda, Takeshi Miyazaki, Takehiro Tsujino, Natsuko Ishii, Ryo Ishikawa, Yukiko Muramoto, Hiroki Grenier, Francois Makino, Yuichi McHugh, Thomas J. Yanagisawa, Masashi Greene, Robert W. Vogt, Kaspar E. |
author_facet | Ohyama, Kaoru Kanda, Takeshi Miyazaki, Takehiro Tsujino, Natsuko Ishii, Ryo Ishikawa, Yukiko Muramoto, Hiroki Grenier, Francois Makino, Yuichi McHugh, Thomas J. Yanagisawa, Masashi Greene, Robert W. Vogt, Kaspar E. |
author_sort | Ohyama, Kaoru |
collection | PubMed |
description | Cortical neurons fire intermittently and synchronously during non-rapid eye movement sleep (NREMS), in which active and silent periods are referred to as ON and OFF periods, respectively. Neuronal firing rates during ON periods (NREMS-ON-activity) are similar to those of wakefulness (W-activity), raising the possibility that NREMS-ON neuronal-activity is fragmented W-activity. To test this, we investigated the patterning and organization of cortical spike trains and of spike ensembles in neuronal networks using extracellular recordings in mice. Firing rates of neurons during NREMS-ON and W were similar, but showed enhanced bursting in NREMS with no apparent preference in occurrence, relative to the beginning or end of the on-state. Additionally, there was an overall increase in the randomness of occurrence of sequences comprised of multi-neuron ensembles in NREMS recorded from tetrodes. In association with increased burst firing, somatic calcium transients were increased in NREMS. The increased calcium transients associated with bursting during NREM may activate calcium-dependent, cell-signaling pathways for sleep related cellular processes. |
format | Online Article Text |
id | pubmed-7259746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72597462020-06-08 Structure of cortical network activity across natural wake and sleep states in mice Ohyama, Kaoru Kanda, Takeshi Miyazaki, Takehiro Tsujino, Natsuko Ishii, Ryo Ishikawa, Yukiko Muramoto, Hiroki Grenier, Francois Makino, Yuichi McHugh, Thomas J. Yanagisawa, Masashi Greene, Robert W. Vogt, Kaspar E. PLoS One Research Article Cortical neurons fire intermittently and synchronously during non-rapid eye movement sleep (NREMS), in which active and silent periods are referred to as ON and OFF periods, respectively. Neuronal firing rates during ON periods (NREMS-ON-activity) are similar to those of wakefulness (W-activity), raising the possibility that NREMS-ON neuronal-activity is fragmented W-activity. To test this, we investigated the patterning and organization of cortical spike trains and of spike ensembles in neuronal networks using extracellular recordings in mice. Firing rates of neurons during NREMS-ON and W were similar, but showed enhanced bursting in NREMS with no apparent preference in occurrence, relative to the beginning or end of the on-state. Additionally, there was an overall increase in the randomness of occurrence of sequences comprised of multi-neuron ensembles in NREMS recorded from tetrodes. In association with increased burst firing, somatic calcium transients were increased in NREMS. The increased calcium transients associated with bursting during NREM may activate calcium-dependent, cell-signaling pathways for sleep related cellular processes. Public Library of Science 2020-05-29 /pmc/articles/PMC7259746/ /pubmed/32470016 http://dx.doi.org/10.1371/journal.pone.0233561 Text en © 2020 Ohyama et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ohyama, Kaoru Kanda, Takeshi Miyazaki, Takehiro Tsujino, Natsuko Ishii, Ryo Ishikawa, Yukiko Muramoto, Hiroki Grenier, Francois Makino, Yuichi McHugh, Thomas J. Yanagisawa, Masashi Greene, Robert W. Vogt, Kaspar E. Structure of cortical network activity across natural wake and sleep states in mice |
title | Structure of cortical network activity across natural wake and sleep states in mice |
title_full | Structure of cortical network activity across natural wake and sleep states in mice |
title_fullStr | Structure of cortical network activity across natural wake and sleep states in mice |
title_full_unstemmed | Structure of cortical network activity across natural wake and sleep states in mice |
title_short | Structure of cortical network activity across natural wake and sleep states in mice |
title_sort | structure of cortical network activity across natural wake and sleep states in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259746/ https://www.ncbi.nlm.nih.gov/pubmed/32470016 http://dx.doi.org/10.1371/journal.pone.0233561 |
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