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How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?

BACKGROUND: Obstructive sleep apnea (OSA) is characterized by repetitive episodes of upper airway collapse during sleep. The contraction of upper airway dilator muscles plays a crucial role in maintaining UA patency. Chronic intermittent hypoxia (CIH) is the most important pathophysiological process...

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Autores principales: Meng, Yanling, Li, Wenyang, Zou, Ying, Yao, Ye, Huang, Hong, Sun, Jianjun, Li, Xiaomeng, Guo, Shu, Zhang, Xilong, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573330/
https://www.ncbi.nlm.nih.gov/pubmed/33117010
http://dx.doi.org/10.2147/NSS.S249948
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author Meng, Yanling
Li, Wenyang
Zou, Ying
Yao, Ye
Huang, Hong
Sun, Jianjun
Li, Xiaomeng
Guo, Shu
Zhang, Xilong
Wang, Wei
author_facet Meng, Yanling
Li, Wenyang
Zou, Ying
Yao, Ye
Huang, Hong
Sun, Jianjun
Li, Xiaomeng
Guo, Shu
Zhang, Xilong
Wang, Wei
author_sort Meng, Yanling
collection PubMed
description BACKGROUND: Obstructive sleep apnea (OSA) is characterized by repetitive episodes of upper airway collapse during sleep. The contraction of upper airway dilator muscles plays a crucial role in maintaining UA patency. Chronic intermittent hypoxia (CIH) is the most important pathophysiological process of OSA. Exposure to CIH induced not only the damage of dilator muscles but also the plasticity of the muscles. This study aimed to dynamically assess the influence of CIH on the upper airway. METHODS: The experiments were performed on 44 rats. They were randomly divided into a normoxia (NO) group (n=22) and CIH group (n=22). In each group (n=6, respectively), EMG, transcranial magnetic stimulation (TMS) response, and critical pressure (Pcrit) value were recorded on day 0 (the day before exposure), and the 7th, 14th, 21st, and 28th day of air/CIH exposure. For each group, 16 rats were used for transmission electron microscopy observations on day 0, and the 7th, 14th and 28th day of air/CIH exposure (n=4 for every time point). RESULTS: Compared to the NO group at the same point, the CIH group showed a damaged ultrastructure of genioglossus, increased activity of genioglossus corticomotor area, and increased Pcrit of the upper airway from the 7th to the 28th day of CIH. Increased EMG activity occurred at the 14th day of CIH and lasted for 2 weeks. CONCLUSION: The elevated genioglossus corticomotor excitability in response to the CIH could not counterbalance the damage effect of CIH on upper airway dilator muscles, which ultimately increased the collapsibility of the upper airway.
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spelling pubmed-75733302020-10-27 How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats? Meng, Yanling Li, Wenyang Zou, Ying Yao, Ye Huang, Hong Sun, Jianjun Li, Xiaomeng Guo, Shu Zhang, Xilong Wang, Wei Nat Sci Sleep Original Research BACKGROUND: Obstructive sleep apnea (OSA) is characterized by repetitive episodes of upper airway collapse during sleep. The contraction of upper airway dilator muscles plays a crucial role in maintaining UA patency. Chronic intermittent hypoxia (CIH) is the most important pathophysiological process of OSA. Exposure to CIH induced not only the damage of dilator muscles but also the plasticity of the muscles. This study aimed to dynamically assess the influence of CIH on the upper airway. METHODS: The experiments were performed on 44 rats. They were randomly divided into a normoxia (NO) group (n=22) and CIH group (n=22). In each group (n=6, respectively), EMG, transcranial magnetic stimulation (TMS) response, and critical pressure (Pcrit) value were recorded on day 0 (the day before exposure), and the 7th, 14th, 21st, and 28th day of air/CIH exposure. For each group, 16 rats were used for transmission electron microscopy observations on day 0, and the 7th, 14th and 28th day of air/CIH exposure (n=4 for every time point). RESULTS: Compared to the NO group at the same point, the CIH group showed a damaged ultrastructure of genioglossus, increased activity of genioglossus corticomotor area, and increased Pcrit of the upper airway from the 7th to the 28th day of CIH. Increased EMG activity occurred at the 14th day of CIH and lasted for 2 weeks. CONCLUSION: The elevated genioglossus corticomotor excitability in response to the CIH could not counterbalance the damage effect of CIH on upper airway dilator muscles, which ultimately increased the collapsibility of the upper airway. Dove 2020-10-15 /pmc/articles/PMC7573330/ /pubmed/33117010 http://dx.doi.org/10.2147/NSS.S249948 Text en © 2020 Meng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Meng, Yanling
Li, Wenyang
Zou, Ying
Yao, Ye
Huang, Hong
Sun, Jianjun
Li, Xiaomeng
Guo, Shu
Zhang, Xilong
Wang, Wei
How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title_full How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title_fullStr How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title_full_unstemmed How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title_short How Does Chronic Intermittent Hypoxia Influence Upper Airway Stability in Rats?
title_sort how does chronic intermittent hypoxia influence upper airway stability in rats?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573330/
https://www.ncbi.nlm.nih.gov/pubmed/33117010
http://dx.doi.org/10.2147/NSS.S249948
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