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Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements

NEW FINDINGS: What is the central question of this study? Is the stabilising function of the diaphragm altered differentially in response to involuntary augmented breaths induced with or without lower‐limb movements? What is the main finding and its importance? At equivalent levels of ventilation, t...

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Autores principales: Illidi, Camilla R., Romer, Lee M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092310/
https://www.ncbi.nlm.nih.gov/pubmed/36177711
http://dx.doi.org/10.1113/EP090605
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author Illidi, Camilla R.
Romer, Lee M.
author_facet Illidi, Camilla R.
Romer, Lee M.
author_sort Illidi, Camilla R.
collection PubMed
description NEW FINDINGS: What is the central question of this study? Is the stabilising function of the diaphragm altered differentially in response to involuntary augmented breaths induced with or without lower‐limb movements? What is the main finding and its importance? At equivalent levels of ventilation, the diaphragm generated higher passive pressure but moved significantly less during incremental cycle ergometry compared with progressive hypercapnia. Diaphragm excursion velocity and power output did not differ between the two tasks. These findings imply that the power output of the diaphragm during stabilising tasks involving the lower limbs may be preserved via coordinated changes in contractile shortening. ABSTRACT: Activity of key respiratory muscles, such as the diaphragm, must balance the demands of ventilation with the maintenance of stable posture. Our aim was to test whether the stabilising function of the diaphragm would be altered differentially in response to involuntary augmented breaths induced with or without lower‐limb movements. Ten healthy volunteers (age 21 (2) years; mean (SD)) performed progressive CO(2)‐rebreathe (5% CO(2), 95% O(2)) followed 20 min later by incremental cycle exercise (15–30 W/min), both in a semi‐recumbent position. Ventilatory indices, intrathoracic pressures and ultrasonographic measures of diaphragm shortening were assessed before, during and after each task. From rest to iso‐time, inspiratory tidal volume and minute ventilation increased two‐ to threefold. At equivalent levels of tidal volume and minute ventilation, mean inspiratory transdiaphragmatic pressure ([Formula: see text]) was consistently higher during exercise compared with CO(2)‐rebreathe due to larger increases in gastric pressure and the passive component of [Formula: see text] (i.e., mechanical output due to static contractions), and yet diaphragm excursion was consistently lower. This lower excursion during exercise was accompanied by a reduction in excursion time with no difference in the active component of [Formula: see text]. Consequently, the rates of increase in excursion velocity (excursion/time) and power output (active [Formula: see text] × velocity) did not differ between the two tasks. In conclusion, the power output of the human diaphragm during dynamic lower‐limb exercise appears to be preserved via coordinated changes in contractile shortening. The findings may have significance in settings where the ventilatory and stabilising functions of the diaphragm must be balanced (e.g., rehabilitation).
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spelling pubmed-100923102023-04-13 Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements Illidi, Camilla R. Romer, Lee M. Exp Physiol Research Articles NEW FINDINGS: What is the central question of this study? Is the stabilising function of the diaphragm altered differentially in response to involuntary augmented breaths induced with or without lower‐limb movements? What is the main finding and its importance? At equivalent levels of ventilation, the diaphragm generated higher passive pressure but moved significantly less during incremental cycle ergometry compared with progressive hypercapnia. Diaphragm excursion velocity and power output did not differ between the two tasks. These findings imply that the power output of the diaphragm during stabilising tasks involving the lower limbs may be preserved via coordinated changes in contractile shortening. ABSTRACT: Activity of key respiratory muscles, such as the diaphragm, must balance the demands of ventilation with the maintenance of stable posture. Our aim was to test whether the stabilising function of the diaphragm would be altered differentially in response to involuntary augmented breaths induced with or without lower‐limb movements. Ten healthy volunteers (age 21 (2) years; mean (SD)) performed progressive CO(2)‐rebreathe (5% CO(2), 95% O(2)) followed 20 min later by incremental cycle exercise (15–30 W/min), both in a semi‐recumbent position. Ventilatory indices, intrathoracic pressures and ultrasonographic measures of diaphragm shortening were assessed before, during and after each task. From rest to iso‐time, inspiratory tidal volume and minute ventilation increased two‐ to threefold. At equivalent levels of tidal volume and minute ventilation, mean inspiratory transdiaphragmatic pressure ([Formula: see text]) was consistently higher during exercise compared with CO(2)‐rebreathe due to larger increases in gastric pressure and the passive component of [Formula: see text] (i.e., mechanical output due to static contractions), and yet diaphragm excursion was consistently lower. This lower excursion during exercise was accompanied by a reduction in excursion time with no difference in the active component of [Formula: see text]. Consequently, the rates of increase in excursion velocity (excursion/time) and power output (active [Formula: see text] × velocity) did not differ between the two tasks. In conclusion, the power output of the human diaphragm during dynamic lower‐limb exercise appears to be preserved via coordinated changes in contractile shortening. The findings may have significance in settings where the ventilatory and stabilising functions of the diaphragm must be balanced (e.g., rehabilitation). John Wiley and Sons Inc. 2022-10-21 2022-12-01 /pmc/articles/PMC10092310/ /pubmed/36177711 http://dx.doi.org/10.1113/EP090605 Text en © 2022 The Authors. Experimental Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Illidi, Camilla R.
Romer, Lee M.
Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title_full Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title_fullStr Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title_full_unstemmed Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title_short Stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
title_sort stabilising function of the human diaphragm in response to involuntary augmented breaths induced with or without lower‐limb movements
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092310/
https://www.ncbi.nlm.nih.gov/pubmed/36177711
http://dx.doi.org/10.1113/EP090605
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