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Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P

The rhythm generating network for breathing must continuously adjust to changing metabolic and behavioral demands. Here, we examined network-based mechanisms in the mouse preBötzinger complex using substance P, a potent excitatory modulator of breathing frequency and stability, as a tool to dissect...

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Detalles Bibliográficos
Autores principales: Baertsch, Nathan A, Ramirez, Jan-Marino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957314/
https://www.ncbi.nlm.nih.gov/pubmed/31804180
http://dx.doi.org/10.7554/eLife.51350
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author Baertsch, Nathan A
Ramirez, Jan-Marino
author_facet Baertsch, Nathan A
Ramirez, Jan-Marino
author_sort Baertsch, Nathan A
collection PubMed
description The rhythm generating network for breathing must continuously adjust to changing metabolic and behavioral demands. Here, we examined network-based mechanisms in the mouse preBötzinger complex using substance P, a potent excitatory modulator of breathing frequency and stability, as a tool to dissect network properties that underlie dynamic breathing. We find that substance P does not alter the balance of excitation and inhibition during breaths or the duration of the resulting refractory period. Instead, mechanisms of recurrent excitation between breaths are enhanced such that the rate that excitation percolates through the network is increased. We propose a conceptual framework in which three distinct phases of inspiration, the burst phase, refractory phase, and percolation phase, can be differentially modulated to control breathing dynamics and stability. Unraveling mechanisms that support this dynamic control may improve our understanding of nervous system disorders that destabilize breathing, many of which involve changes in brainstem neuromodulatory systems.
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spelling pubmed-69573142020-01-15 Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P Baertsch, Nathan A Ramirez, Jan-Marino eLife Neuroscience The rhythm generating network for breathing must continuously adjust to changing metabolic and behavioral demands. Here, we examined network-based mechanisms in the mouse preBötzinger complex using substance P, a potent excitatory modulator of breathing frequency and stability, as a tool to dissect network properties that underlie dynamic breathing. We find that substance P does not alter the balance of excitation and inhibition during breaths or the duration of the resulting refractory period. Instead, mechanisms of recurrent excitation between breaths are enhanced such that the rate that excitation percolates through the network is increased. We propose a conceptual framework in which three distinct phases of inspiration, the burst phase, refractory phase, and percolation phase, can be differentially modulated to control breathing dynamics and stability. Unraveling mechanisms that support this dynamic control may improve our understanding of nervous system disorders that destabilize breathing, many of which involve changes in brainstem neuromodulatory systems. eLife Sciences Publications, Ltd 2019-12-05 /pmc/articles/PMC6957314/ /pubmed/31804180 http://dx.doi.org/10.7554/eLife.51350 Text en © 2019, Baertsch and Ramirez http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Baertsch, Nathan A
Ramirez, Jan-Marino
Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title_full Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title_fullStr Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title_full_unstemmed Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title_short Insights into the dynamic control of breathing revealed through cell-type-specific responses to substance P
title_sort insights into the dynamic control of breathing revealed through cell-type-specific responses to substance p
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957314/
https://www.ncbi.nlm.nih.gov/pubmed/31804180
http://dx.doi.org/10.7554/eLife.51350
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