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Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain
Frequent nightly arousals typical for sleep disorders cause daytime fatigue and present health risks. As such arousals are often short, partial, or occur locally within the brain, reliable characterization in rodent models of sleep disorders and in human patients is challenging. We found that the EE...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291975/ https://www.ncbi.nlm.nih.gov/pubmed/34227936 http://dx.doi.org/10.7554/eLife.65835 |
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author | Cardis, Romain Lecci, Sandro Fernandez, Laura MJ Osorio-Forero, Alejandro Chu Sin Chung, Paul Fulda, Stephany Decosterd, Isabelle Lüthi, Anita |
author_facet | Cardis, Romain Lecci, Sandro Fernandez, Laura MJ Osorio-Forero, Alejandro Chu Sin Chung, Paul Fulda, Stephany Decosterd, Isabelle Lüthi, Anita |
author_sort | Cardis, Romain |
collection | PubMed |
description | Frequent nightly arousals typical for sleep disorders cause daytime fatigue and present health risks. As such arousals are often short, partial, or occur locally within the brain, reliable characterization in rodent models of sleep disorders and in human patients is challenging. We found that the EEG spectral composition of non-rapid eye movement sleep (NREMS) in healthy mice shows an infraslow (~50 s) interval over which microarousals appear preferentially. NREMS could hence be vulnerable to abnormal arousals on this time scale. Chronic pain is well-known to disrupt sleep. In the spared nerve injury (SNI) mouse model of chronic neuropathic pain, we found more numerous local cortical arousals accompanied by heart rate increases in hindlimb primary somatosensory, but not in prelimbic, cortices, although sleep macroarchitecture appeared unaltered. Closed-loop mechanovibrational stimulation further revealed higher sensory arousability. Chronic pain thus preserved conventional sleep measures but resulted in elevated spontaneous and evoked arousability. We develop a novel moment-to-moment probing of NREMS vulnerability and propose that chronic pain-induced sleep complaints arise from perturbed arousability. |
format | Online Article Text |
id | pubmed-8291975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-82919752021-07-21 Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain Cardis, Romain Lecci, Sandro Fernandez, Laura MJ Osorio-Forero, Alejandro Chu Sin Chung, Paul Fulda, Stephany Decosterd, Isabelle Lüthi, Anita eLife Neuroscience Frequent nightly arousals typical for sleep disorders cause daytime fatigue and present health risks. As such arousals are often short, partial, or occur locally within the brain, reliable characterization in rodent models of sleep disorders and in human patients is challenging. We found that the EEG spectral composition of non-rapid eye movement sleep (NREMS) in healthy mice shows an infraslow (~50 s) interval over which microarousals appear preferentially. NREMS could hence be vulnerable to abnormal arousals on this time scale. Chronic pain is well-known to disrupt sleep. In the spared nerve injury (SNI) mouse model of chronic neuropathic pain, we found more numerous local cortical arousals accompanied by heart rate increases in hindlimb primary somatosensory, but not in prelimbic, cortices, although sleep macroarchitecture appeared unaltered. Closed-loop mechanovibrational stimulation further revealed higher sensory arousability. Chronic pain thus preserved conventional sleep measures but resulted in elevated spontaneous and evoked arousability. We develop a novel moment-to-moment probing of NREMS vulnerability and propose that chronic pain-induced sleep complaints arise from perturbed arousability. eLife Sciences Publications, Ltd 2021-07-06 /pmc/articles/PMC8291975/ /pubmed/34227936 http://dx.doi.org/10.7554/eLife.65835 Text en © 2021, Cardis et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Cardis, Romain Lecci, Sandro Fernandez, Laura MJ Osorio-Forero, Alejandro Chu Sin Chung, Paul Fulda, Stephany Decosterd, Isabelle Lüthi, Anita Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title | Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title_full | Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title_fullStr | Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title_full_unstemmed | Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title_short | Cortico-autonomic local arousals and heightened somatosensory arousability during NREMS of mice in neuropathic pain |
title_sort | cortico-autonomic local arousals and heightened somatosensory arousability during nrems of mice in neuropathic pain |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291975/ https://www.ncbi.nlm.nih.gov/pubmed/34227936 http://dx.doi.org/10.7554/eLife.65835 |
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