HUMAN RESPIRATORY MUSCLES: SENSATIONS, REFLEXES AND FATIGUABILITY
SUMMARY 1. Given the importance of the ventilatory ‘pump’ muscles, it would not be surprising if they were endowed with both sensory and motor specializations. The present review focuses on some unexpected properties of the respiratory muscle system in human subjects. 2. Although changes in blood ga...
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Veröffentlicht in: | Clinical and experimental pharmacology & physiology 1998-10, Vol.25 (10), p.757-763 |
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creator | Gandevia, SC Allen, GM Butler, JE Gorman, RB McKenzie, DK |
description | SUMMARY
1. Given the importance of the ventilatory ‘pump’ muscles, it would not be surprising if they were endowed with both sensory and motor specializations. The present review focuses on some unexpected properties of the respiratory muscle system in human subjects.
2. Although changes in blood gas tension were long held not to influence sensation directly, studies in subjects who are completely paralysed show that increases in arterial CO2 levels elicit strong sensations of respiratory discomfort.
3. Stretch reflexes in human limb muscles contain a monosynaptic spinal excitation and a long‐latency excitation. However, inspiratory muscles show an initial inhibition when tested with brief airway occlusions during inspiration. This inhibition does not depend critically on input from pulmonary or upper airway receptors.
4. Human inspiratory muscles (including the diaphragm) have been considered to fatigue during inspiratory resistive loading. However, recent studies using phrenic nerve stimulation to test the force produced by the diaphragm show that carbon dioxide retention (hypoventilation) and voluntary cessation of loading occur before the muscles become overtly fatigued. |
doi_str_mv | 10.1111/j.1440-1681.1998.tb02150.x |
format | Article |
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1. Given the importance of the ventilatory ‘pump’ muscles, it would not be surprising if they were endowed with both sensory and motor specializations. The present review focuses on some unexpected properties of the respiratory muscle system in human subjects.
2. Although changes in blood gas tension were long held not to influence sensation directly, studies in subjects who are completely paralysed show that increases in arterial CO2 levels elicit strong sensations of respiratory discomfort.
3. Stretch reflexes in human limb muscles contain a monosynaptic spinal excitation and a long‐latency excitation. However, inspiratory muscles show an initial inhibition when tested with brief airway occlusions during inspiration. This inhibition does not depend critically on input from pulmonary or upper airway receptors.
4. Human inspiratory muscles (including the diaphragm) have been considered to fatigue during inspiratory resistive loading. However, recent studies using phrenic nerve stimulation to test the force produced by the diaphragm show that carbon dioxide retention (hypoventilation) and voluntary cessation of loading occur before the muscles become overtly fatigued.</description><identifier>ISSN: 0305-1870</identifier><identifier>EISSN: 1440-1681</identifier><identifier>DOI: 10.1111/j.1440-1681.1998.tb02150.x</identifier><identifier>PMID: 9784913</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>carbon dioxide ; Carbon Dioxide - physiology ; Chemoreceptor Cells - physiology ; diaphragm ; dyspnoea ; fatigue ; Humans ; J reflex ; Muscle Fatigue ; Reflex ; Respiratory Insufficiency - physiopathology ; Respiratory Mechanics - physiology ; Respiratory Muscles - innervation ; Respiratory Muscles - physiology ; Sensation ; stretch reflex</subject><ispartof>Clinical and experimental pharmacology & physiology, 1998-10, Vol.25 (10), p.757-763</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4077-9f2e6d12877ad7c0979cad966bc82dfc85ffe32991d33ac3e58cab71cd92fb673</citedby><cites>FETCH-LOGICAL-c4077-9f2e6d12877ad7c0979cad966bc82dfc85ffe32991d33ac3e58cab71cd92fb673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1440-1681.1998.tb02150.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1440-1681.1998.tb02150.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9784913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gandevia, SC</creatorcontrib><creatorcontrib>Allen, GM</creatorcontrib><creatorcontrib>Butler, JE</creatorcontrib><creatorcontrib>Gorman, RB</creatorcontrib><creatorcontrib>McKenzie, DK</creatorcontrib><title>HUMAN RESPIRATORY MUSCLES: SENSATIONS, REFLEXES AND FATIGUABILITY</title><title>Clinical and experimental pharmacology & physiology</title><addtitle>Clin Exp Pharmacol Physiol</addtitle><description>SUMMARY
1. Given the importance of the ventilatory ‘pump’ muscles, it would not be surprising if they were endowed with both sensory and motor specializations. The present review focuses on some unexpected properties of the respiratory muscle system in human subjects.
2. Although changes in blood gas tension were long held not to influence sensation directly, studies in subjects who are completely paralysed show that increases in arterial CO2 levels elicit strong sensations of respiratory discomfort.
3. Stretch reflexes in human limb muscles contain a monosynaptic spinal excitation and a long‐latency excitation. However, inspiratory muscles show an initial inhibition when tested with brief airway occlusions during inspiration. This inhibition does not depend critically on input from pulmonary or upper airway receptors.
4. Human inspiratory muscles (including the diaphragm) have been considered to fatigue during inspiratory resistive loading. However, recent studies using phrenic nerve stimulation to test the force produced by the diaphragm show that carbon dioxide retention (hypoventilation) and voluntary cessation of loading occur before the muscles become overtly fatigued.</description><subject>carbon dioxide</subject><subject>Carbon Dioxide - physiology</subject><subject>Chemoreceptor Cells - physiology</subject><subject>diaphragm</subject><subject>dyspnoea</subject><subject>fatigue</subject><subject>Humans</subject><subject>J reflex</subject><subject>Muscle Fatigue</subject><subject>Reflex</subject><subject>Respiratory Insufficiency - physiopathology</subject><subject>Respiratory Mechanics - physiology</subject><subject>Respiratory Muscles - innervation</subject><subject>Respiratory Muscles - physiology</subject><subject>Sensation</subject><subject>stretch reflex</subject><issn>0305-1870</issn><issn>1440-1681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEFPg0AQhTdGU2v1J5gQD54Ed1mWZT2YYKWUhNKmtNqeNrAsCZXayrax_fdCaHp3LpPMe_Mm8wHwgKCB6npeGciyoI5sBxmIMcfYpdBEBBqHC9A9S5egCzEkOnIovAY3Sq0ghATauAM6jDoWQ7gL3OF85Eba1IsnwdSdjadLbTSP-6EXv2ixF8XuLBhH8VNtGITewos1N3rXBvXUn7tvQRjMlrfgKk9KJe9OvQfmA2_WH-rh2A_6bqgLC1Kqs9yUdoZMh9IkowIyykSSMdtOhWNmuXBInktsMoYyjBOBJXFEklIkMmbmqU1xDzy2udtq87OXasfXhRKyLJNvudkrbrOahMVgbXxpjaLaKFXJnG-rYp1UR44gb_jxFW8g8QYSb_jxEz9-qJfvT1f26Vpm59UTsFp_bfXfopTHfyTzvjehpHlDbwMKtZOHc0BSffH6SUr4Z-TzD3_hY2LafIL_AH6xiUA</recordid><startdate>199810</startdate><enddate>199810</enddate><creator>Gandevia, SC</creator><creator>Allen, GM</creator><creator>Butler, JE</creator><creator>Gorman, RB</creator><creator>McKenzie, DK</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199810</creationdate><title>HUMAN RESPIRATORY MUSCLES: SENSATIONS, REFLEXES AND FATIGUABILITY</title><author>Gandevia, SC ; Allen, GM ; Butler, JE ; Gorman, RB ; McKenzie, DK</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4077-9f2e6d12877ad7c0979cad966bc82dfc85ffe32991d33ac3e58cab71cd92fb673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>carbon dioxide</topic><topic>Carbon Dioxide - physiology</topic><topic>Chemoreceptor Cells - physiology</topic><topic>diaphragm</topic><topic>dyspnoea</topic><topic>fatigue</topic><topic>Humans</topic><topic>J reflex</topic><topic>Muscle Fatigue</topic><topic>Reflex</topic><topic>Respiratory Insufficiency - physiopathology</topic><topic>Respiratory Mechanics - physiology</topic><topic>Respiratory Muscles - innervation</topic><topic>Respiratory Muscles - physiology</topic><topic>Sensation</topic><topic>stretch reflex</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gandevia, SC</creatorcontrib><creatorcontrib>Allen, GM</creatorcontrib><creatorcontrib>Butler, JE</creatorcontrib><creatorcontrib>Gorman, RB</creatorcontrib><creatorcontrib>McKenzie, DK</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental pharmacology & physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gandevia, SC</au><au>Allen, GM</au><au>Butler, JE</au><au>Gorman, RB</au><au>McKenzie, DK</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HUMAN RESPIRATORY MUSCLES: SENSATIONS, REFLEXES AND FATIGUABILITY</atitle><jtitle>Clinical and experimental pharmacology & physiology</jtitle><addtitle>Clin Exp Pharmacol Physiol</addtitle><date>1998-10</date><risdate>1998</risdate><volume>25</volume><issue>10</issue><spage>757</spage><epage>763</epage><pages>757-763</pages><issn>0305-1870</issn><eissn>1440-1681</eissn><abstract>SUMMARY
1. Given the importance of the ventilatory ‘pump’ muscles, it would not be surprising if they were endowed with both sensory and motor specializations. The present review focuses on some unexpected properties of the respiratory muscle system in human subjects.
2. Although changes in blood gas tension were long held not to influence sensation directly, studies in subjects who are completely paralysed show that increases in arterial CO2 levels elicit strong sensations of respiratory discomfort.
3. Stretch reflexes in human limb muscles contain a monosynaptic spinal excitation and a long‐latency excitation. However, inspiratory muscles show an initial inhibition when tested with brief airway occlusions during inspiration. This inhibition does not depend critically on input from pulmonary or upper airway receptors.
4. Human inspiratory muscles (including the diaphragm) have been considered to fatigue during inspiratory resistive loading. However, recent studies using phrenic nerve stimulation to test the force produced by the diaphragm show that carbon dioxide retention (hypoventilation) and voluntary cessation of loading occur before the muscles become overtly fatigued.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9784913</pmid><doi>10.1111/j.1440-1681.1998.tb02150.x</doi><tpages>7</tpages></addata></record> |
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subjects | carbon dioxide Carbon Dioxide - physiology Chemoreceptor Cells - physiology diaphragm dyspnoea fatigue Humans J reflex Muscle Fatigue Reflex Respiratory Insufficiency - physiopathology Respiratory Mechanics - physiology Respiratory Muscles - innervation Respiratory Muscles - physiology Sensation stretch reflex |
title | HUMAN RESPIRATORY MUSCLES: SENSATIONS, REFLEXES AND FATIGUABILITY |
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