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Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway

Obstructive sleep apnea (OSA) patients have increased upper airway muscle activity, including such lingual muscles as the genioglossus (GG), geniohyoid (GH), and hyoglossus (HG). This adaptation partially protects their upper airway against obstructions. Rodents are used to study the central neural...

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Autores principales: Rukhadze, Irma, Kalter, Julie, Stettner, Georg M., Kubin, Leszek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009435/
https://www.ncbi.nlm.nih.gov/pubmed/24803913
http://dx.doi.org/10.3389/fneur.2014.00061
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author Rukhadze, Irma
Kalter, Julie
Stettner, Georg M.
Kubin, Leszek
author_facet Rukhadze, Irma
Kalter, Julie
Stettner, Georg M.
Kubin, Leszek
author_sort Rukhadze, Irma
collection PubMed
description Obstructive sleep apnea (OSA) patients have increased upper airway muscle activity, including such lingual muscles as the genioglossus (GG), geniohyoid (GH), and hyoglossus (HG). This adaptation partially protects their upper airway against obstructions. Rodents are used to study the central neural control of sleep and breathing but they do not naturally exhibit OSA. We investigated whether, in chronically instrumented, behaving rats, disconnecting the GH and HG muscles from the hyoid (H) apparatus would result in a compensatory increase of other upper airway muscle activity (electromyogram, EMG) and/or other signs of upper airway instability. We first determined that, in intact rats, lingual (GG and intrinsic) muscles maintained stable activity levels when quantified based on 2 h-long recordings conducted on days 6 through 22 after instrumentation. We then studied five rats in which the tendons connecting the GH and HG muscles to the H apparatus were experimentally severed. When quantified across all recording days, lingual EMG during slow-wave sleep (SWS) was modestly but significantly increased in rats with surgically altered upper airway [8.6 ± 0.7% (SE) vs. 6.1 ± 0.7% of the mean during wakefulness; p = 0.012]. Respiratory modulation of lingual EMG occurred mainly during SWS and was similarly infrequent in both groups, and the incidence of sighs and central apneas also was similar. Thus, a weakened action of selected lingual muscles did not produce sleep-disordered breathing but resulted in a relatively elevated activity in other lingual muscles during SWS. These results encourage more extensive surgical manipulations with the aim to obtain a rodent model with collapsible upper airway.
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spelling pubmed-40094352014-05-06 Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway Rukhadze, Irma Kalter, Julie Stettner, Georg M. Kubin, Leszek Front Neurol Neuroscience Obstructive sleep apnea (OSA) patients have increased upper airway muscle activity, including such lingual muscles as the genioglossus (GG), geniohyoid (GH), and hyoglossus (HG). This adaptation partially protects their upper airway against obstructions. Rodents are used to study the central neural control of sleep and breathing but they do not naturally exhibit OSA. We investigated whether, in chronically instrumented, behaving rats, disconnecting the GH and HG muscles from the hyoid (H) apparatus would result in a compensatory increase of other upper airway muscle activity (electromyogram, EMG) and/or other signs of upper airway instability. We first determined that, in intact rats, lingual (GG and intrinsic) muscles maintained stable activity levels when quantified based on 2 h-long recordings conducted on days 6 through 22 after instrumentation. We then studied five rats in which the tendons connecting the GH and HG muscles to the H apparatus were experimentally severed. When quantified across all recording days, lingual EMG during slow-wave sleep (SWS) was modestly but significantly increased in rats with surgically altered upper airway [8.6 ± 0.7% (SE) vs. 6.1 ± 0.7% of the mean during wakefulness; p = 0.012]. Respiratory modulation of lingual EMG occurred mainly during SWS and was similarly infrequent in both groups, and the incidence of sighs and central apneas also was similar. Thus, a weakened action of selected lingual muscles did not produce sleep-disordered breathing but resulted in a relatively elevated activity in other lingual muscles during SWS. These results encourage more extensive surgical manipulations with the aim to obtain a rodent model with collapsible upper airway. Frontiers Media S.A. 2014-04-28 /pmc/articles/PMC4009435/ /pubmed/24803913 http://dx.doi.org/10.3389/fneur.2014.00061 Text en Copyright © 2014 Rukhadze, Kalter, Stettner and Kubin. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Rukhadze, Irma
Kalter, Julie
Stettner, Georg M.
Kubin, Leszek
Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title_full Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title_fullStr Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title_full_unstemmed Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title_short Lingual Muscle Activity Across Sleep–Wake States in Rats with Surgically Altered Upper Airway
title_sort lingual muscle activity across sleep–wake states in rats with surgically altered upper airway
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009435/
https://www.ncbi.nlm.nih.gov/pubmed/24803913
http://dx.doi.org/10.3389/fneur.2014.00061
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