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Mechanisms of sympathetic regulation during Apnea

Volitional Apnea produces a robust peak sympathetic response through several interacting mechanisms. However, the specific contribution of each mechanism has not been elucidated. Muscle sympathetic activity was collected in participants (n = 10; 24 ± 3 years) that performed four maximal volitional a...

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Autores principales: Busch, Stephen A., Bruce, Christina D., Skow, Rachel J., Pfoh, Jaime R., Day, Trevor A., Davenport, Margie H., Steinback, Craig D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349657/
https://www.ncbi.nlm.nih.gov/pubmed/30693670
http://dx.doi.org/10.14814/phy2.13991
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author Busch, Stephen A.
Bruce, Christina D.
Skow, Rachel J.
Pfoh, Jaime R.
Day, Trevor A.
Davenport, Margie H.
Steinback, Craig D.
author_facet Busch, Stephen A.
Bruce, Christina D.
Skow, Rachel J.
Pfoh, Jaime R.
Day, Trevor A.
Davenport, Margie H.
Steinback, Craig D.
author_sort Busch, Stephen A.
collection PubMed
description Volitional Apnea produces a robust peak sympathetic response through several interacting mechanisms. However, the specific contribution of each mechanism has not been elucidated. Muscle sympathetic activity was collected in participants (n = 10; 24 ± 3 years) that performed four maximal volitional apneas aimed at isolating lung‐stretch (mechanical) and chemoreflex drive: (Ainslie and Duffin 2009) end‐expiratory breath‐hold, (Ainslie et al. 2013) end‐inspiratory breath‐hold, (Alpher et al. 1986) prehyperventilation breath‐hold, and (Andersson and Schagatay 1998) prehyperoxia breath‐hold. A final repeated rebreathe breath‐hold protocol was performed to measure the peak sympathetic response during successive breath‐holds at increasing chemoreflex stress. Finally, the influence of dynamic ventilation was assessed through asphyxic rebreathe. Muscle sympathetic activity was calculated as the change in burst frequency (burst/min), burst incidence (burst/100 heart‐beats), and amplitude (au) between baseline and prevolitional breakpoint. Rebreathe was analyzed at similar chemoreflex stress as inspiratory breath‐hold. All maneuvers increased muscle sympathetic activity compared to baseline (P < 0.01). However, prehyperoxia exhibited a smaller increase (+22.18 ± 9.13 burst/min; +25.52 ± 11.7 burst/100 heart‐beats) compared to inspiratory, expiratory, and prehyperventilation breath‐holds. At similar chemoreflex strain, rebreathe sympathetic activity was blunted compared to inspiratory breath‐hold (P < 0.01). Finally, muscle sympathetic activity was not different between the repeated rebreathe trials, despite elevated chemoreflex stress and lower breath‐hold duration with each subsequent breath‐hold. We have demonstrated an obligatory role of the peripheral, but not central, chemoreflex (prehyperventilation vs. prehyperoxia) in producing peak sympathetic responses. At similar chemoreflex stresses the act of dynamic ventilation, but not static lung stretch per se, blunts muscle sympathetic activity. Finally, similar peak sympathetic responses during successive repeated breath‐holds suggest a sympathetic ceiling may exist.
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spelling pubmed-63496572019-01-31 Mechanisms of sympathetic regulation during Apnea Busch, Stephen A. Bruce, Christina D. Skow, Rachel J. Pfoh, Jaime R. Day, Trevor A. Davenport, Margie H. Steinback, Craig D. Physiol Rep Original Research Volitional Apnea produces a robust peak sympathetic response through several interacting mechanisms. However, the specific contribution of each mechanism has not been elucidated. Muscle sympathetic activity was collected in participants (n = 10; 24 ± 3 years) that performed four maximal volitional apneas aimed at isolating lung‐stretch (mechanical) and chemoreflex drive: (Ainslie and Duffin 2009) end‐expiratory breath‐hold, (Ainslie et al. 2013) end‐inspiratory breath‐hold, (Alpher et al. 1986) prehyperventilation breath‐hold, and (Andersson and Schagatay 1998) prehyperoxia breath‐hold. A final repeated rebreathe breath‐hold protocol was performed to measure the peak sympathetic response during successive breath‐holds at increasing chemoreflex stress. Finally, the influence of dynamic ventilation was assessed through asphyxic rebreathe. Muscle sympathetic activity was calculated as the change in burst frequency (burst/min), burst incidence (burst/100 heart‐beats), and amplitude (au) between baseline and prevolitional breakpoint. Rebreathe was analyzed at similar chemoreflex stress as inspiratory breath‐hold. All maneuvers increased muscle sympathetic activity compared to baseline (P < 0.01). However, prehyperoxia exhibited a smaller increase (+22.18 ± 9.13 burst/min; +25.52 ± 11.7 burst/100 heart‐beats) compared to inspiratory, expiratory, and prehyperventilation breath‐holds. At similar chemoreflex strain, rebreathe sympathetic activity was blunted compared to inspiratory breath‐hold (P < 0.01). Finally, muscle sympathetic activity was not different between the repeated rebreathe trials, despite elevated chemoreflex stress and lower breath‐hold duration with each subsequent breath‐hold. We have demonstrated an obligatory role of the peripheral, but not central, chemoreflex (prehyperventilation vs. prehyperoxia) in producing peak sympathetic responses. At similar chemoreflex stresses the act of dynamic ventilation, but not static lung stretch per se, blunts muscle sympathetic activity. Finally, similar peak sympathetic responses during successive repeated breath‐holds suggest a sympathetic ceiling may exist. John Wiley and Sons Inc. 2019-01-28 /pmc/articles/PMC6349657/ /pubmed/30693670 http://dx.doi.org/10.14814/phy2.13991 Text en © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Busch, Stephen A.
Bruce, Christina D.
Skow, Rachel J.
Pfoh, Jaime R.
Day, Trevor A.
Davenport, Margie H.
Steinback, Craig D.
Mechanisms of sympathetic regulation during Apnea
title Mechanisms of sympathetic regulation during Apnea
title_full Mechanisms of sympathetic regulation during Apnea
title_fullStr Mechanisms of sympathetic regulation during Apnea
title_full_unstemmed Mechanisms of sympathetic regulation during Apnea
title_short Mechanisms of sympathetic regulation during Apnea
title_sort mechanisms of sympathetic regulation during apnea
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349657/
https://www.ncbi.nlm.nih.gov/pubmed/30693670
http://dx.doi.org/10.14814/phy2.13991
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