Respiratory sensations, cardiovascular control, kinaesthesia and transcranial stimulation during paralysis in humans
1. To determine whether discomfort associated with breathing (dyspnoea) is related to the chemical drive to breath, three subjects were totally paralysed while fully conscious. Subjective responses to a rising CO2 stimulus were obtained during rebreathing, rebreathing with CO2 added, and breath hold...
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creator | Gandevia, S C Killian, K McKenzie, D K Crawford, M Allen, G M Gorman, R B Hales, J P |
description | 1. To determine whether discomfort associated with breathing (dyspnoea) is related to the chemical drive to breath, three
subjects were totally paralysed while fully conscious. Subjective responses to a rising CO2 stimulus were obtained during
rebreathing, rebreathing with CO2 added, and breath holding. Dyspnoea was measured with a 10-point Borg scale. 2. Following
nasotracheal intubation and ventilation (oxygen saturation, O2,Sat, 98-100% and end-tidal CO2, PET,CO2, 30-40 mmHg), total
neuromuscular blockade was induced by a rapid injection of atracurium (> 2.5 mg kg-1) and complete paralysis was maintained
with an infusion (5 mg (kg h)-1). Paralysis was confirmed by abolition of the compound muscle action potentials of both the
diaphragm and abductor hallucis evoked by supramaximal electrical stimulation of the relevant nerves. Communication via finger
movement was preserved for the first 20-30 min following paralysis by inflation of a sphygmomanometer cuff on one arm. 3.
Before and during complete paralysis, dyspnoea increased progressively during hypercapnia produced by rebreathing (with or
without CO2 added to the circuit at 250 ml min-1). The mean PET,CO2 eliciting 'severe' dyspnoea was 46 mmHg during rebreathing,
42 mmHg during 'breath holding', and 52 mmHg during rebreathing with added CO2. There were no significant differences between
the values obtained during paralysis and in the control study immediately before paralysis. The duration of breath holding
was not prolonged by paralysis and the PET,CO2 at the 'break point' was not altered by paralysis. 4. Thus, dyspnoea is preserved
following total neuromuscular blockade. This suggests that chemoreceptor activity, via the central neuronal activity which
it evokes, can lead to discomfort in the absence of any contraction of respiratory muscles. 5. During paralysis, attempted
contraction of arm, leg and trunk muscles increased heart rate and blood pressure. For attempted handgrip contractions, the
increases in heart rate (range, 7-15 beats min-1) and mean arterial pressure (range, 20-32 mmHg) were similar to those recorded
with actual contractions in trials immediately before paralysis. In one subject, graded increases in heart rate and blood
pressure occurred for attempted contractions of 45 s duration over a range of intensities (0-100% maximal effort). 6. During
complete paralysis, transcranial electromagnetic stimulation of the motor cortex produced illusory twitch-like movements of
the wrist and |
doi_str_mv | 10.1113/jphysiol.1993.sp019849 |
format | Article |
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subjects were totally paralysed while fully conscious. Subjective responses to a rising CO2 stimulus were obtained during
rebreathing, rebreathing with CO2 added, and breath holding. Dyspnoea was measured with a 10-point Borg scale. 2. Following
nasotracheal intubation and ventilation (oxygen saturation, O2,Sat, 98-100% and end-tidal CO2, PET,CO2, 30-40 mmHg), total
neuromuscular blockade was induced by a rapid injection of atracurium (> 2.5 mg kg-1) and complete paralysis was maintained
with an infusion (5 mg (kg h)-1). Paralysis was confirmed by abolition of the compound muscle action potentials of both the
diaphragm and abductor hallucis evoked by supramaximal electrical stimulation of the relevant nerves. Communication via finger
movement was preserved for the first 20-30 min following paralysis by inflation of a sphygmomanometer cuff on one arm. 3.
Before and during complete paralysis, dyspnoea increased progressively during hypercapnia produced by rebreathing (with or
without CO2 added to the circuit at 250 ml min-1). The mean PET,CO2 eliciting 'severe' dyspnoea was 46 mmHg during rebreathing,
42 mmHg during 'breath holding', and 52 mmHg during rebreathing with added CO2. There were no significant differences between
the values obtained during paralysis and in the control study immediately before paralysis. The duration of breath holding
was not prolonged by paralysis and the PET,CO2 at the 'break point' was not altered by paralysis. 4. Thus, dyspnoea is preserved
following total neuromuscular blockade. This suggests that chemoreceptor activity, via the central neuronal activity which
it evokes, can lead to discomfort in the absence of any contraction of respiratory muscles. 5. During paralysis, attempted
contraction of arm, leg and trunk muscles increased heart rate and blood pressure. For attempted handgrip contractions, the
increases in heart rate (range, 7-15 beats min-1) and mean arterial pressure (range, 20-32 mmHg) were similar to those recorded
with actual contractions in trials immediately before paralysis. In one subject, graded increases in heart rate and blood
pressure occurred for attempted contractions of 45 s duration over a range of intensities (0-100% maximal effort). 6. During
complete paralysis, transcranial electromagnetic stimulation of the motor cortex produced illusory twitch-like movements of
the wrist and digits. This also occurred in separate studies during complete ischaemic paralysis and anaesthesia of the forearm
and hand.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.1993.sp019849</identifier><identifier>PMID: 8308755</identifier><identifier>CODEN: JPHYA7</identifier><language>eng</language><publisher>Oxford: The Physiological Society</publisher><subject>Action Potentials - physiology ; Biological and medical sciences ; Blood Pressure - physiology ; Dyspnea - physiopathology ; Electric Stimulation ; Hemodynamics - physiology ; Humans ; Hypercapnia - physiopathology ; Kinesthesis - physiology ; Magnetics ; Male ; Medical sciences ; Motor Cortex - physiology ; Paralysis - chemically induced ; Paralysis - physiopathology ; Pneumology ; Respiratory Mechanics - physiology ; Respiratory system : syndromes and miscellaneous diseases</subject><ispartof>The Journal of physiology, 1993-10, Vol.470 (1), p.85-107</ispartof><rights>1993 The Physiological Society</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6265-41ed9386dd702077a948c2189ddac053c1719bed1ddd38d477f83c584c85dcf23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1143908/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1143908/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,1412,27905,27906,45555,45556,53772,53774</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3757823$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8308755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gandevia, S C</creatorcontrib><creatorcontrib>Killian, K</creatorcontrib><creatorcontrib>McKenzie, D K</creatorcontrib><creatorcontrib>Crawford, M</creatorcontrib><creatorcontrib>Allen, G M</creatorcontrib><creatorcontrib>Gorman, R B</creatorcontrib><creatorcontrib>Hales, J P</creatorcontrib><title>Respiratory sensations, cardiovascular control, kinaesthesia and transcranial stimulation during paralysis in humans</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>1. To determine whether discomfort associated with breathing (dyspnoea) is related to the chemical drive to breath, three
subjects were totally paralysed while fully conscious. Subjective responses to a rising CO2 stimulus were obtained during
rebreathing, rebreathing with CO2 added, and breath holding. Dyspnoea was measured with a 10-point Borg scale. 2. Following
nasotracheal intubation and ventilation (oxygen saturation, O2,Sat, 98-100% and end-tidal CO2, PET,CO2, 30-40 mmHg), total
neuromuscular blockade was induced by a rapid injection of atracurium (> 2.5 mg kg-1) and complete paralysis was maintained
with an infusion (5 mg (kg h)-1). Paralysis was confirmed by abolition of the compound muscle action potentials of both the
diaphragm and abductor hallucis evoked by supramaximal electrical stimulation of the relevant nerves. Communication via finger
movement was preserved for the first 20-30 min following paralysis by inflation of a sphygmomanometer cuff on one arm. 3.
Before and during complete paralysis, dyspnoea increased progressively during hypercapnia produced by rebreathing (with or
without CO2 added to the circuit at 250 ml min-1). The mean PET,CO2 eliciting 'severe' dyspnoea was 46 mmHg during rebreathing,
42 mmHg during 'breath holding', and 52 mmHg during rebreathing with added CO2. There were no significant differences between
the values obtained during paralysis and in the control study immediately before paralysis. The duration of breath holding
was not prolonged by paralysis and the PET,CO2 at the 'break point' was not altered by paralysis. 4. Thus, dyspnoea is preserved
following total neuromuscular blockade. This suggests that chemoreceptor activity, via the central neuronal activity which
it evokes, can lead to discomfort in the absence of any contraction of respiratory muscles. 5. During paralysis, attempted
contraction of arm, leg and trunk muscles increased heart rate and blood pressure. For attempted handgrip contractions, the
increases in heart rate (range, 7-15 beats min-1) and mean arterial pressure (range, 20-32 mmHg) were similar to those recorded
with actual contractions in trials immediately before paralysis. In one subject, graded increases in heart rate and blood
pressure occurred for attempted contractions of 45 s duration over a range of intensities (0-100% maximal effort). 6. During
complete paralysis, transcranial electromagnetic stimulation of the motor cortex produced illusory twitch-like movements of
the wrist and digits. This also occurred in separate studies during complete ischaemic paralysis and anaesthesia of the forearm
and hand.</description><subject>Action Potentials - physiology</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Dyspnea - physiopathology</subject><subject>Electric Stimulation</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Hypercapnia - physiopathology</subject><subject>Kinesthesis - physiology</subject><subject>Magnetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Motor Cortex - physiology</subject><subject>Paralysis - chemically induced</subject><subject>Paralysis - physiopathology</subject><subject>Pneumology</subject><subject>Respiratory Mechanics - physiology</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxSMEKtvCRwD5gFAPzeKJk9i-IFUVf1UJhMrZcm1n4-KNgydptd8eR7tdwY2LLXl-896MX1G8BroGAPbubux36GNYg5RsjSMFKWr5pFhB3cqSc8meFitKq6pkvIHnxSniHaXAqJQnxYlgVPCmWRXTD4ejT3qKaUfQDagnHwe8IEYn6-O9RjMHnYiJw5RiuCC__KAdTr1Dr4keLJmSHtDkw-tAcPLbzC8axM7JDxsy6qRDHhWJH0g_bzP9onjW6YDu5eE-K35-_HBz9bm8_vbpy9XldWnaqm3KGpyVTLTWclpRzrWshalASGu1oQ0zwEHeOgvWWiZszXknmGlEbURjTVexs-L9Xnecb7fOGpd30EGNyW912qmovfq3MvhebeK9AqiZpCILnB8EUvw957XV1qNxIejBxRkVtC2toa744tXuUZMiYnLd0QaoWhJTj4mpJTH1mFhufPX3kMe2Q0S5_uZQz1no0OWfNh6PWE6Xi4pl7HKPPfjgdv9prm6-fl8eak5BLFZv9xq93_QPPjm178JovJt2KmMKVAb_AFw4yQg</recordid><startdate>19931001</startdate><enddate>19931001</enddate><creator>Gandevia, S C</creator><creator>Killian, K</creator><creator>McKenzie, D K</creator><creator>Crawford, M</creator><creator>Allen, G M</creator><creator>Gorman, R B</creator><creator>Hales, J P</creator><general>The Physiological Society</general><general>Blackwell</general><scope>IQODW</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>7QR</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>19931001</creationdate><title>Respiratory sensations, cardiovascular control, kinaesthesia and transcranial stimulation during paralysis in humans</title><author>Gandevia, S C ; Killian, K ; McKenzie, D K ; Crawford, M ; Allen, G M ; Gorman, R B ; Hales, J P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6265-41ed9386dd702077a948c2189ddac053c1719bed1ddd38d477f83c584c85dcf23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Action Potentials - physiology</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - physiology</topic><topic>Dyspnea - physiopathology</topic><topic>Electric Stimulation</topic><topic>Hemodynamics - physiology</topic><topic>Humans</topic><topic>Hypercapnia - physiopathology</topic><topic>Kinesthesis - physiology</topic><topic>Magnetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Motor Cortex - physiology</topic><topic>Paralysis - chemically induced</topic><topic>Paralysis - physiopathology</topic><topic>Pneumology</topic><topic>Respiratory Mechanics - physiology</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gandevia, S C</creatorcontrib><creatorcontrib>Killian, K</creatorcontrib><creatorcontrib>McKenzie, D K</creatorcontrib><creatorcontrib>Crawford, M</creatorcontrib><creatorcontrib>Allen, G M</creatorcontrib><creatorcontrib>Gorman, R B</creatorcontrib><creatorcontrib>Hales, J P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gandevia, S C</au><au>Killian, K</au><au>McKenzie, D K</au><au>Crawford, M</au><au>Allen, G M</au><au>Gorman, R B</au><au>Hales, J P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Respiratory sensations, cardiovascular control, kinaesthesia and transcranial stimulation during paralysis in humans</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>1993-10-01</date><risdate>1993</risdate><volume>470</volume><issue>1</issue><spage>85</spage><epage>107</epage><pages>85-107</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><coden>JPHYA7</coden><abstract>1. To determine whether discomfort associated with breathing (dyspnoea) is related to the chemical drive to breath, three
subjects were totally paralysed while fully conscious. Subjective responses to a rising CO2 stimulus were obtained during
rebreathing, rebreathing with CO2 added, and breath holding. Dyspnoea was measured with a 10-point Borg scale. 2. Following
nasotracheal intubation and ventilation (oxygen saturation, O2,Sat, 98-100% and end-tidal CO2, PET,CO2, 30-40 mmHg), total
neuromuscular blockade was induced by a rapid injection of atracurium (> 2.5 mg kg-1) and complete paralysis was maintained
with an infusion (5 mg (kg h)-1). Paralysis was confirmed by abolition of the compound muscle action potentials of both the
diaphragm and abductor hallucis evoked by supramaximal electrical stimulation of the relevant nerves. Communication via finger
movement was preserved for the first 20-30 min following paralysis by inflation of a sphygmomanometer cuff on one arm. 3.
Before and during complete paralysis, dyspnoea increased progressively during hypercapnia produced by rebreathing (with or
without CO2 added to the circuit at 250 ml min-1). The mean PET,CO2 eliciting 'severe' dyspnoea was 46 mmHg during rebreathing,
42 mmHg during 'breath holding', and 52 mmHg during rebreathing with added CO2. There were no significant differences between
the values obtained during paralysis and in the control study immediately before paralysis. The duration of breath holding
was not prolonged by paralysis and the PET,CO2 at the 'break point' was not altered by paralysis. 4. Thus, dyspnoea is preserved
following total neuromuscular blockade. This suggests that chemoreceptor activity, via the central neuronal activity which
it evokes, can lead to discomfort in the absence of any contraction of respiratory muscles. 5. During paralysis, attempted
contraction of arm, leg and trunk muscles increased heart rate and blood pressure. For attempted handgrip contractions, the
increases in heart rate (range, 7-15 beats min-1) and mean arterial pressure (range, 20-32 mmHg) were similar to those recorded
with actual contractions in trials immediately before paralysis. In one subject, graded increases in heart rate and blood
pressure occurred for attempted contractions of 45 s duration over a range of intensities (0-100% maximal effort). 6. During
complete paralysis, transcranial electromagnetic stimulation of the motor cortex produced illusory twitch-like movements of
the wrist and digits. This also occurred in separate studies during complete ischaemic paralysis and anaesthesia of the forearm
and hand.</abstract><cop>Oxford</cop><pub>The Physiological Society</pub><pmid>8308755</pmid><doi>10.1113/jphysiol.1993.sp019849</doi><tpages>23</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; IngentaConnect Free/Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Action Potentials - physiology Biological and medical sciences Blood Pressure - physiology Dyspnea - physiopathology Electric Stimulation Hemodynamics - physiology Humans Hypercapnia - physiopathology Kinesthesis - physiology Magnetics Male Medical sciences Motor Cortex - physiology Paralysis - chemically induced Paralysis - physiopathology Pneumology Respiratory Mechanics - physiology Respiratory system : syndromes and miscellaneous diseases |
title | Respiratory sensations, cardiovascular control, kinaesthesia and transcranial stimulation during paralysis in humans |
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