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Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice

Periodic Cheyne–Stokes breathing (CSB) oscillating between apnea and crescendo–decrescendo hyperpnea is the most common central apnea. Currently, there is no proven therapy for CSB, probably because the fundamental pathophysiological question of how the respiratory center generates this form of brea...

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Autores principales: Casarrubios, Ana M., Pérez-Atencio, Leonel F., Martín, Cristina, Ibarz, José M., Mañas, Eva, Paul, David L., Barrio, Luis C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944137/
https://www.ncbi.nlm.nih.gov/pubmed/36845442
http://dx.doi.org/10.3389/fnins.2023.1045269
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author Casarrubios, Ana M.
Pérez-Atencio, Leonel F.
Martín, Cristina
Ibarz, José M.
Mañas, Eva
Paul, David L.
Barrio, Luis C.
author_facet Casarrubios, Ana M.
Pérez-Atencio, Leonel F.
Martín, Cristina
Ibarz, José M.
Mañas, Eva
Paul, David L.
Barrio, Luis C.
author_sort Casarrubios, Ana M.
collection PubMed
description Periodic Cheyne–Stokes breathing (CSB) oscillating between apnea and crescendo–decrescendo hyperpnea is the most common central apnea. Currently, there is no proven therapy for CSB, probably because the fundamental pathophysiological question of how the respiratory center generates this form of breathing instability is still unresolved. Therefore, we aimed to determine the respiratory motor pattern of CSB resulting from the interaction of inspiratory and expiratory oscillators and identify the neural mechanism responsible for breathing regularization induced by the supplemental CO(2) administration. Analysis of the inspiratory and expiratory motor pattern in a transgenic mouse model lacking connexin-36 electrical synapses, the neonatal (P14) Cx36 knockout male mouse, with a persistent CSB, revealed that the reconfigurations recurrent between apnea and hyperpnea and vice versa result from cyclical turn on/off of active expiration driven by the expiratory oscillator, which acts as a master pacemaker of respiration and entrains the inspiratory oscillator to restore ventilation. The results also showed that the suppression of CSB by supplemental 12% CO(2) in inhaled air is due to the stabilization of coupling between expiratory and inspiratory oscillators, which causes the regularization of respiration. CSB rebooted after washout of CO(2) excess when the inspiratory activity depressed again profoundly, indicating that the disability of the inspiratory oscillator to sustain ventilation is the triggering factor of CSB. Under these circumstances, the expiratory oscillator activated by the cyclic increase of CO(2) behaves as an “anti-apnea” center generating the crescendo–decrescendo hyperpnea and periodic breathing. The neurogenic mechanism of CSB identified highlights the plasticity of the two-oscillator system in the neural control of respiration and provides a rationale base for CO(2) therapy.
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spelling pubmed-99441372023-02-23 Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice Casarrubios, Ana M. Pérez-Atencio, Leonel F. Martín, Cristina Ibarz, José M. Mañas, Eva Paul, David L. Barrio, Luis C. Front Neurosci Neuroscience Periodic Cheyne–Stokes breathing (CSB) oscillating between apnea and crescendo–decrescendo hyperpnea is the most common central apnea. Currently, there is no proven therapy for CSB, probably because the fundamental pathophysiological question of how the respiratory center generates this form of breathing instability is still unresolved. Therefore, we aimed to determine the respiratory motor pattern of CSB resulting from the interaction of inspiratory and expiratory oscillators and identify the neural mechanism responsible for breathing regularization induced by the supplemental CO(2) administration. Analysis of the inspiratory and expiratory motor pattern in a transgenic mouse model lacking connexin-36 electrical synapses, the neonatal (P14) Cx36 knockout male mouse, with a persistent CSB, revealed that the reconfigurations recurrent between apnea and hyperpnea and vice versa result from cyclical turn on/off of active expiration driven by the expiratory oscillator, which acts as a master pacemaker of respiration and entrains the inspiratory oscillator to restore ventilation. The results also showed that the suppression of CSB by supplemental 12% CO(2) in inhaled air is due to the stabilization of coupling between expiratory and inspiratory oscillators, which causes the regularization of respiration. CSB rebooted after washout of CO(2) excess when the inspiratory activity depressed again profoundly, indicating that the disability of the inspiratory oscillator to sustain ventilation is the triggering factor of CSB. Under these circumstances, the expiratory oscillator activated by the cyclic increase of CO(2) behaves as an “anti-apnea” center generating the crescendo–decrescendo hyperpnea and periodic breathing. The neurogenic mechanism of CSB identified highlights the plasticity of the two-oscillator system in the neural control of respiration and provides a rationale base for CO(2) therapy. Frontiers Media S.A. 2023-02-08 /pmc/articles/PMC9944137/ /pubmed/36845442 http://dx.doi.org/10.3389/fnins.2023.1045269 Text en Copyright © 2023 Casarrubios, Pérez-Atencio, Martín, Ibarz, Mañas, Paul and Barrio. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Casarrubios, Ana M.
Pérez-Atencio, Leonel F.
Martín, Cristina
Ibarz, José M.
Mañas, Eva
Paul, David L.
Barrio, Luis C.
Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title_full Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title_fullStr Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title_full_unstemmed Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title_short Neural bases for the genesis and CO(2) therapy of periodic Cheyne–Stokes breathing in neonatal male connexin-36 knockout mice
title_sort neural bases for the genesis and co(2) therapy of periodic cheyne–stokes breathing in neonatal male connexin-36 knockout mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944137/
https://www.ncbi.nlm.nih.gov/pubmed/36845442
http://dx.doi.org/10.3389/fnins.2023.1045269
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