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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...

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Autores principales: Cardis, Romain, Lecci, Sandro, Fernandez, Laura MJ, Osorio-Forero, Alejandro, Chu Sin Chung, Paul, Fulda, Stephany, Decosterd, Isabelle, Lüthi, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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