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Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo

Motoneurons are the final output pathway for the brain’s influence on behavior. Here we identify properties of hypoglossal motor output to the tongue musculature. Tongue motor control is critical to the pathogenesis of obstructive sleep apnea, a common and serious sleep-related breathing disorder. S...

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Autores principales: Aggarwal, Jasmin A., Liu, Wen-Ying, Montandon, Gaspard, Liu, Hattie, Hughes, Stuart W., Horner, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969049/
https://www.ncbi.nlm.nih.gov/pubmed/31953471
http://dx.doi.org/10.1038/s41598-019-57328-4
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author Aggarwal, Jasmin A.
Liu, Wen-Ying
Montandon, Gaspard
Liu, Hattie
Hughes, Stuart W.
Horner, Richard L.
author_facet Aggarwal, Jasmin A.
Liu, Wen-Ying
Montandon, Gaspard
Liu, Hattie
Hughes, Stuart W.
Horner, Richard L.
author_sort Aggarwal, Jasmin A.
collection PubMed
description Motoneurons are the final output pathway for the brain’s influence on behavior. Here we identify properties of hypoglossal motor output to the tongue musculature. Tongue motor control is critical to the pathogenesis of obstructive sleep apnea, a common and serious sleep-related breathing disorder. Studies were performed on mice expressing a light sensitive cation channel exclusively on cholinergic neurons (ChAT-ChR2(H134R)-EYFP). Discrete photostimulations under isoflurane-induced anesthesia from an optical probe positioned above the medullary surface and hypoglossal motor nucleus elicited discrete increases in tongue motor output, with the magnitude of responses dependent on stimulation power (P < 0.001, n = 7) and frequency (P = 0.002, n = 8, with responses to 10 Hz stimulation greater than for 15–25 Hz, P < 0.022). Stimulations during REM sleep elicited significantly reduced responses at powers 3–20 mW compared to non-rapid eye movement (non-REM) sleep and wakefulness (each P < 0.05, n = 7). Response thresholds were also greater in REM sleep (10 mW) compared to non-REM and waking (3 to 5 mW, P < 0.05), and the slopes of the regressions between input photostimulation powers and output motor responses were specifically reduced in REM sleep (P < 0.001). This study identifies that variations in photostimulation input produce tunable changes in hypoglossal motor output in-vivo and identifies REM sleep specific suppression of net motor excitability and responsivity.
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spelling pubmed-69690492020-01-22 Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo Aggarwal, Jasmin A. Liu, Wen-Ying Montandon, Gaspard Liu, Hattie Hughes, Stuart W. Horner, Richard L. Sci Rep Article Motoneurons are the final output pathway for the brain’s influence on behavior. Here we identify properties of hypoglossal motor output to the tongue musculature. Tongue motor control is critical to the pathogenesis of obstructive sleep apnea, a common and serious sleep-related breathing disorder. Studies were performed on mice expressing a light sensitive cation channel exclusively on cholinergic neurons (ChAT-ChR2(H134R)-EYFP). Discrete photostimulations under isoflurane-induced anesthesia from an optical probe positioned above the medullary surface and hypoglossal motor nucleus elicited discrete increases in tongue motor output, with the magnitude of responses dependent on stimulation power (P < 0.001, n = 7) and frequency (P = 0.002, n = 8, with responses to 10 Hz stimulation greater than for 15–25 Hz, P < 0.022). Stimulations during REM sleep elicited significantly reduced responses at powers 3–20 mW compared to non-rapid eye movement (non-REM) sleep and wakefulness (each P < 0.05, n = 7). Response thresholds were also greater in REM sleep (10 mW) compared to non-REM and waking (3 to 5 mW, P < 0.05), and the slopes of the regressions between input photostimulation powers and output motor responses were specifically reduced in REM sleep (P < 0.001). This study identifies that variations in photostimulation input produce tunable changes in hypoglossal motor output in-vivo and identifies REM sleep specific suppression of net motor excitability and responsivity. Nature Publishing Group UK 2020-01-17 /pmc/articles/PMC6969049/ /pubmed/31953471 http://dx.doi.org/10.1038/s41598-019-57328-4 Text en © The Author(s) 2020 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/.
spellingShingle Article
Aggarwal, Jasmin A.
Liu, Wen-Ying
Montandon, Gaspard
Liu, Hattie
Hughes, Stuart W.
Horner, Richard L.
Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title_full Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title_fullStr Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title_full_unstemmed Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title_short Measurement and State-Dependent Modulation of Hypoglossal Motor Excitability and Responsivity In-Vivo
title_sort measurement and state-dependent modulation of hypoglossal motor excitability and responsivity in-vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969049/
https://www.ncbi.nlm.nih.gov/pubmed/31953471
http://dx.doi.org/10.1038/s41598-019-57328-4
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