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After-discharge in the upper airway muscle genioglossus following brief hypoxia
Abstract Study Objectives Genioglossus (GG) after-discharge is thought to protect against pharyngeal collapse by minimizing periods of low upper airway muscle activity. How GG after-discharge occurs and which single motor units (SMUs) are responsible for the phenomenon are unknown. The aim of this s...
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Published in: | Sleep (New York, N.Y.) N.Y.), 2021-09, Vol.44 (9), p.1 |
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creator | Avraam, Joanne Dawson, Andrew Feast, Nicole Fan, Feiven Lee Fridgant, Monika D Kay, Amanda Koay, Zi Yi Jia, Pingdong Greig, Rachel Thornton, Therese Nicholas, Christian L O’Donoghue, Fergal J Trinder, John Jordan, Amy S |
description | Abstract
Study Objectives
Genioglossus (GG) after-discharge is thought to protect against pharyngeal collapse by minimizing periods of low upper airway muscle activity. How GG after-discharge occurs and which single motor units (SMUs) are responsible for the phenomenon are unknown. The aim of this study was to investigate genioglossal after-discharge.
Methods
During wakefulness, after-discharge was elicited 8–12 times in healthy individuals with brief isocapnic hypoxia (45–60 s of 10% O2 in N2) terminated by a single breath of 100% O2. GG SMUs were designated as firing solely, or at increased rate, during inspiration (Inspiratory phasic [IP] and inspiratory tonic [IT], respectively); solely, or at increased rate, during expiration (Expiratory phasic [EP] or expiratory tonic [ET], respectively) or firing constantly without respiratory modulation (Tonic). SMUs were quantified at baseline, the end of hypoxia, the hyperoxic breath, and the following eight normoxic breaths.
Results
A total of 210 SMUs were identified in 17 participants. GG muscle activity was elevated above baseline for seven breaths after hyperoxia (p < 0.001), indicating a strong after-discharge effect. After-discharge occurred due to persistent firing of IP and IT units that were recruited during hypoxia, with minimal changes in ET, EP, or Tonic SMUs. The firing frequency of units that were already active changed minimally during hypoxia or the afterdischarge period (p > 0.05).
Conclusion
That genioglossal after-discharge is almost entirely due to persistent firing of previously silent inspiratory SMUs provides insight into the mechanisms responsible for the phenomenon and supports the hypothesis that the inspiratory and expiratory/tonic motor units within the muscle have idiosyncratic functions. |
doi_str_mv | 10.1093/sleep/zsab084 |
format | article |
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Study Objectives
Genioglossus (GG) after-discharge is thought to protect against pharyngeal collapse by minimizing periods of low upper airway muscle activity. How GG after-discharge occurs and which single motor units (SMUs) are responsible for the phenomenon are unknown. The aim of this study was to investigate genioglossal after-discharge.
Methods
During wakefulness, after-discharge was elicited 8–12 times in healthy individuals with brief isocapnic hypoxia (45–60 s of 10% O2 in N2) terminated by a single breath of 100% O2. GG SMUs were designated as firing solely, or at increased rate, during inspiration (Inspiratory phasic [IP] and inspiratory tonic [IT], respectively); solely, or at increased rate, during expiration (Expiratory phasic [EP] or expiratory tonic [ET], respectively) or firing constantly without respiratory modulation (Tonic). SMUs were quantified at baseline, the end of hypoxia, the hyperoxic breath, and the following eight normoxic breaths.
Results
A total of 210 SMUs were identified in 17 participants. GG muscle activity was elevated above baseline for seven breaths after hyperoxia (p < 0.001), indicating a strong after-discharge effect. After-discharge occurred due to persistent firing of IP and IT units that were recruited during hypoxia, with minimal changes in ET, EP, or Tonic SMUs. The firing frequency of units that were already active changed minimally during hypoxia or the afterdischarge period (p > 0.05).
Conclusion
That genioglossal after-discharge is almost entirely due to persistent firing of previously silent inspiratory SMUs provides insight into the mechanisms responsible for the phenomenon and supports the hypothesis that the inspiratory and expiratory/tonic motor units within the muscle have idiosyncratic functions.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsab084</identifier><identifier>PMID: 33822200</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Alcohol ; Hypoxia ; Muscle function ; Sleep ; Sleep apnea ; Sleep apnea syndromes</subject><ispartof>Sleep (New York, N.Y.), 2021-09, Vol.44 (9), p.1</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2021</rights><rights>Sleep Research Society 2021. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2021 Oxford University Press</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4115-71f5b3562f1f6aa13f5eb1f5b07683d3dae17b3c25d59739d5af7811fb3660983</citedby><cites>FETCH-LOGICAL-c4115-71f5b3562f1f6aa13f5eb1f5b07683d3dae17b3c25d59739d5af7811fb3660983</cites><orcidid>0000-0002-3837-3609 ; 0000-0001-8561-9766</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33822200$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Avraam, Joanne</creatorcontrib><creatorcontrib>Dawson, Andrew</creatorcontrib><creatorcontrib>Feast, Nicole</creatorcontrib><creatorcontrib>Fan, Feiven Lee</creatorcontrib><creatorcontrib>Fridgant, Monika D</creatorcontrib><creatorcontrib>Kay, Amanda</creatorcontrib><creatorcontrib>Koay, Zi Yi</creatorcontrib><creatorcontrib>Jia, Pingdong</creatorcontrib><creatorcontrib>Greig, Rachel</creatorcontrib><creatorcontrib>Thornton, Therese</creatorcontrib><creatorcontrib>Nicholas, Christian L</creatorcontrib><creatorcontrib>O’Donoghue, Fergal J</creatorcontrib><creatorcontrib>Trinder, John</creatorcontrib><creatorcontrib>Jordan, Amy S</creatorcontrib><title>After-discharge in the upper airway muscle genioglossus following brief hypoxia</title><title>Sleep (New York, N.Y.)</title><addtitle>Sleep</addtitle><description>Abstract
Study Objectives
Genioglossus (GG) after-discharge is thought to protect against pharyngeal collapse by minimizing periods of low upper airway muscle activity. How GG after-discharge occurs and which single motor units (SMUs) are responsible for the phenomenon are unknown. The aim of this study was to investigate genioglossal after-discharge.
Methods
During wakefulness, after-discharge was elicited 8–12 times in healthy individuals with brief isocapnic hypoxia (45–60 s of 10% O2 in N2) terminated by a single breath of 100% O2. GG SMUs were designated as firing solely, or at increased rate, during inspiration (Inspiratory phasic [IP] and inspiratory tonic [IT], respectively); solely, or at increased rate, during expiration (Expiratory phasic [EP] or expiratory tonic [ET], respectively) or firing constantly without respiratory modulation (Tonic). SMUs were quantified at baseline, the end of hypoxia, the hyperoxic breath, and the following eight normoxic breaths.
Results
A total of 210 SMUs were identified in 17 participants. GG muscle activity was elevated above baseline for seven breaths after hyperoxia (p < 0.001), indicating a strong after-discharge effect. After-discharge occurred due to persistent firing of IP and IT units that were recruited during hypoxia, with minimal changes in ET, EP, or Tonic SMUs. The firing frequency of units that were already active changed minimally during hypoxia or the afterdischarge period (p > 0.05).
Conclusion
That genioglossal after-discharge is almost entirely due to persistent firing of previously silent inspiratory SMUs provides insight into the mechanisms responsible for the phenomenon and supports the hypothesis that the inspiratory and expiratory/tonic motor units within the muscle have idiosyncratic functions.</description><subject>Alcohol</subject><subject>Hypoxia</subject><subject>Muscle function</subject><subject>Sleep</subject><subject>Sleep apnea</subject><subject>Sleep apnea syndromes</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkU1P3DAQhq2qCJaFY6-VpV64hPVHnMTHFSpQCYkLnC0nGWeNnDjYGy3Lr68XFlatKlU-jDzzzKuZeRH6RsklJZIvogMYF69R16TKv6AZFYJkMpW-ohmhBc0qSsQJOo3xiaR_LvkxOuG8YowRMkP3S7OGkLU2NisdOsB2wOsV4GkcIWBtw0ZvcT_FxgHuYLC-cz7GKWLjnfMbO3S4DhYMXm1H_2L1GToy2kU438c5erz--XB1m93d3_y6Wt5lTU6pyEpqRM1FwQw1hdaUGwH1LkfKouItbzXQsuYNE62QJZet0KasKDU1LwoiKz5HF--6Y_DPE8S16tMK4JwewE9RMUEkSyjjCf3xF_rkpzCk6RJVCp4XspQHqtMOlB2MXwfd7ETVsiSECc5YnqjLf1DptdDbxg9gbMr_0ZC9NzQh3S2AUWOwvQ5bRYnaGajeDFR7AxP_fT_sVPfQftIfjh0W99P4H63f-OukGA</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Avraam, Joanne</creator><creator>Dawson, Andrew</creator><creator>Feast, Nicole</creator><creator>Fan, Feiven Lee</creator><creator>Fridgant, Monika D</creator><creator>Kay, Amanda</creator><creator>Koay, Zi Yi</creator><creator>Jia, Pingdong</creator><creator>Greig, Rachel</creator><creator>Thornton, Therese</creator><creator>Nicholas, Christian L</creator><creator>O’Donoghue, Fergal J</creator><creator>Trinder, John</creator><creator>Jordan, Amy S</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3837-3609</orcidid><orcidid>https://orcid.org/0000-0001-8561-9766</orcidid></search><sort><creationdate>20210901</creationdate><title>After-discharge in the upper airway muscle genioglossus following brief hypoxia</title><author>Avraam, Joanne ; Dawson, Andrew ; Feast, Nicole ; Fan, Feiven Lee ; Fridgant, Monika D ; Kay, Amanda ; Koay, Zi Yi ; Jia, Pingdong ; Greig, Rachel ; Thornton, Therese ; Nicholas, Christian L ; O’Donoghue, Fergal J ; Trinder, John ; Jordan, Amy S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4115-71f5b3562f1f6aa13f5eb1f5b07683d3dae17b3c25d59739d5af7811fb3660983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alcohol</topic><topic>Hypoxia</topic><topic>Muscle function</topic><topic>Sleep</topic><topic>Sleep apnea</topic><topic>Sleep apnea syndromes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avraam, Joanne</creatorcontrib><creatorcontrib>Dawson, Andrew</creatorcontrib><creatorcontrib>Feast, Nicole</creatorcontrib><creatorcontrib>Fan, Feiven Lee</creatorcontrib><creatorcontrib>Fridgant, Monika D</creatorcontrib><creatorcontrib>Kay, Amanda</creatorcontrib><creatorcontrib>Koay, Zi Yi</creatorcontrib><creatorcontrib>Jia, Pingdong</creatorcontrib><creatorcontrib>Greig, Rachel</creatorcontrib><creatorcontrib>Thornton, Therese</creatorcontrib><creatorcontrib>Nicholas, Christian L</creatorcontrib><creatorcontrib>O’Donoghue, Fergal J</creatorcontrib><creatorcontrib>Trinder, John</creatorcontrib><creatorcontrib>Jordan, Amy S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Avraam, Joanne</au><au>Dawson, Andrew</au><au>Feast, Nicole</au><au>Fan, Feiven Lee</au><au>Fridgant, Monika D</au><au>Kay, Amanda</au><au>Koay, Zi Yi</au><au>Jia, Pingdong</au><au>Greig, Rachel</au><au>Thornton, Therese</au><au>Nicholas, Christian L</au><au>O’Donoghue, Fergal J</au><au>Trinder, John</au><au>Jordan, Amy S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>After-discharge in the upper airway muscle genioglossus following brief hypoxia</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><addtitle>Sleep</addtitle><date>2021-09-01</date><risdate>2021</risdate><volume>44</volume><issue>9</issue><spage>1</spage><pages>1-</pages><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>Abstract
Study Objectives
Genioglossus (GG) after-discharge is thought to protect against pharyngeal collapse by minimizing periods of low upper airway muscle activity. How GG after-discharge occurs and which single motor units (SMUs) are responsible for the phenomenon are unknown. The aim of this study was to investigate genioglossal after-discharge.
Methods
During wakefulness, after-discharge was elicited 8–12 times in healthy individuals with brief isocapnic hypoxia (45–60 s of 10% O2 in N2) terminated by a single breath of 100% O2. GG SMUs were designated as firing solely, or at increased rate, during inspiration (Inspiratory phasic [IP] and inspiratory tonic [IT], respectively); solely, or at increased rate, during expiration (Expiratory phasic [EP] or expiratory tonic [ET], respectively) or firing constantly without respiratory modulation (Tonic). SMUs were quantified at baseline, the end of hypoxia, the hyperoxic breath, and the following eight normoxic breaths.
Results
A total of 210 SMUs were identified in 17 participants. GG muscle activity was elevated above baseline for seven breaths after hyperoxia (p < 0.001), indicating a strong after-discharge effect. After-discharge occurred due to persistent firing of IP and IT units that were recruited during hypoxia, with minimal changes in ET, EP, or Tonic SMUs. The firing frequency of units that were already active changed minimally during hypoxia or the afterdischarge period (p > 0.05).
Conclusion
That genioglossal after-discharge is almost entirely due to persistent firing of previously silent inspiratory SMUs provides insight into the mechanisms responsible for the phenomenon and supports the hypothesis that the inspiratory and expiratory/tonic motor units within the muscle have idiosyncratic functions.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>33822200</pmid><doi>10.1093/sleep/zsab084</doi><orcidid>https://orcid.org/0000-0002-3837-3609</orcidid><orcidid>https://orcid.org/0000-0001-8561-9766</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford Journals Online; Alma/SFX Local Collection |
subjects | Alcohol Hypoxia Muscle function Sleep Sleep apnea Sleep apnea syndromes |
title | After-discharge in the upper airway muscle genioglossus following brief hypoxia |
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