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Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling

Bibliographic Details
Main Author: John, S. R.
Publication Date: 2024
Other Authors: Barnett, W. H., Abdala, A. P.L., Zoccal, D. B. [UNESP], Rubin, J. E., Molkov, Y. I.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1113/JP285158
https://hdl.handle.net/11449/306458
Summary: Abstract: The Kölliker–Fuse nucleus (KF), which is part of the parabrachial complex, participates in the generation of eupnoea under resting conditions and the control of active abdominal expiration when increased ventilation is required. Moreover, dysfunctions in KF neuronal activity are believed to play a role in the emergence of respiratory abnormalities seen in Rett syndrome (RTT), a progressive neurodevelopmental disorder associated with an irregular breathing pattern and frequent apnoeas. Relatively little is known, however, about the intrinsic dynamics of neurons within the KF and how their synaptic connections affect breathing pattern control and contribute to breathing irregularities. In this study, we use a reduced computational model to consider several dynamical regimes of KF activity paired with different input sources to determine which combinations are compatible with known experimental observations. We further build on these findings to identify possible interactions between the KF and other components of the respiratory neural circuitry. Specifically, we present two models that both simulate eupnoeic as well as RTT-like breathing phenotypes. Using nullcline analysis, we identify the types of inhibitory inputs to the KF leading to RTT-like respiratory patterns and suggest possible KF local circuit organizations. When the identified properties are present, the two models also exhibit quantal acceleration of late-expiratory activity, a hallmark of active expiration featuring forced exhalation, with increasing inhibition to KF, as reported experimentally. Hence, these models instantiate plausible hypotheses about possible KF dynamics and forms of local network interactions, thus providing a general framework as well as specific predictions for future experimental testing. (Figure presented.). Key points: The Kölliker–Fuse nucleus (KF), a part of the parabrachial complex, is involved in regulating normal breathing and controlling active abdominal expiration during increased ventilation. Dysfunction in KF neuronal activity is thought to contribute to respiratory abnormalities seen in Rett syndrome (RTT). This study utilizes computational modelling to explore different dynamical regimes of KF activity and their compatibility with experimental observations. By analysing different model configurations, the study identifies inhibitory inputs to the KF that lead to RTT-like respiratory patterns and proposes potential KF local circuit organizations. Two models are presented that simulate both normal breathing and RTT-like breathing patterns. These models provide testable hypotheses and specific predictions for future experimental investigations, offering a general framework for understanding KF dynamics and potential network interactions.
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spelling Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modellingcontrol of breathingKölliker–FusemodellingRett syndromeAbstract: The Kölliker–Fuse nucleus (KF), which is part of the parabrachial complex, participates in the generation of eupnoea under resting conditions and the control of active abdominal expiration when increased ventilation is required. Moreover, dysfunctions in KF neuronal activity are believed to play a role in the emergence of respiratory abnormalities seen in Rett syndrome (RTT), a progressive neurodevelopmental disorder associated with an irregular breathing pattern and frequent apnoeas. Relatively little is known, however, about the intrinsic dynamics of neurons within the KF and how their synaptic connections affect breathing pattern control and contribute to breathing irregularities. In this study, we use a reduced computational model to consider several dynamical regimes of KF activity paired with different input sources to determine which combinations are compatible with known experimental observations. We further build on these findings to identify possible interactions between the KF and other components of the respiratory neural circuitry. Specifically, we present two models that both simulate eupnoeic as well as RTT-like breathing phenotypes. Using nullcline analysis, we identify the types of inhibitory inputs to the KF leading to RTT-like respiratory patterns and suggest possible KF local circuit organizations. When the identified properties are present, the two models also exhibit quantal acceleration of late-expiratory activity, a hallmark of active expiration featuring forced exhalation, with increasing inhibition to KF, as reported experimentally. Hence, these models instantiate plausible hypotheses about possible KF dynamics and forms of local network interactions, thus providing a general framework as well as specific predictions for future experimental testing. (Figure presented.). Key points: The Kölliker–Fuse nucleus (KF), a part of the parabrachial complex, is involved in regulating normal breathing and controlling active abdominal expiration during increased ventilation. Dysfunction in KF neuronal activity is thought to contribute to respiratory abnormalities seen in Rett syndrome (RTT). This study utilizes computational modelling to explore different dynamical regimes of KF activity and their compatibility with experimental observations. By analysing different model configurations, the study identifies inhibitory inputs to the KF that lead to RTT-like respiratory patterns and proposes potential KF local circuit organizations. Two models are presented that simulate both normal breathing and RTT-like breathing patterns. These models provide testable hypotheses and specific predictions for future experimental investigations, offering a general framework for understanding KF dynamics and potential network interactions.Georgia State UniversityConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)National Science FoundationNational Center for Complementary and Integrative HealthUniversity of PittsburghIndiana University Purdue University IndianapolisUniversity of BristolSão Paulo State UniversityGeorgia State UniversitySão Paulo State UniversityCNPq: 303481/2021-8National Science Foundation: DMS 1951095National Center for Complementary and Integrative Health: R01AT008632University of PittsburghIndiana University Purdue University IndianapolisUniversity of BristolUniversidade Estadual Paulista (UNESP)Georgia State UniversityJohn, S. R.Barnett, W. H.Abdala, A. P.L.Zoccal, D. B. [UNESP]Rubin, J. E.Molkov, Y. I.2025-04-29T20:06:18Z2024-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article93-112http://dx.doi.org/10.1113/JP285158Journal of Physiology, v. 602, n. 1, p. 93-112, 2024.1469-77930022-3751https://hdl.handle.net/11449/30645810.1113/JP2851582-s2.0-85178966285Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Physiologyinfo:eu-repo/semantics/openAccess2025-04-30T13:53:31Zoai:repositorio.unesp.br:11449/306458Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T13:53:31Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
title Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
spellingShingle Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
John, S. R.
control of breathing
Kölliker–Fuse
modelling
Rett syndrome
title_short Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
title_full Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
title_fullStr Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
title_full_unstemmed Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
title_sort Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
author John, S. R.
author_facet John, S. R.
Barnett, W. H.
Abdala, A. P.L.
Zoccal, D. B. [UNESP]
Rubin, J. E.
Molkov, Y. I.
author_role author
author2 Barnett, W. H.
Abdala, A. P.L.
Zoccal, D. B. [UNESP]
Rubin, J. E.
Molkov, Y. I.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv University of Pittsburgh
Indiana University Purdue University Indianapolis
University of Bristol
Universidade Estadual Paulista (UNESP)
Georgia State University
dc.contributor.author.fl_str_mv John, S. R.
Barnett, W. H.
Abdala, A. P.L.
Zoccal, D. B. [UNESP]
Rubin, J. E.
Molkov, Y. I.
dc.subject.por.fl_str_mv control of breathing
Kölliker–Fuse
modelling
Rett syndrome
topic control of breathing
Kölliker–Fuse
modelling
Rett syndrome
description Abstract: The Kölliker–Fuse nucleus (KF), which is part of the parabrachial complex, participates in the generation of eupnoea under resting conditions and the control of active abdominal expiration when increased ventilation is required. Moreover, dysfunctions in KF neuronal activity are believed to play a role in the emergence of respiratory abnormalities seen in Rett syndrome (RTT), a progressive neurodevelopmental disorder associated with an irregular breathing pattern and frequent apnoeas. Relatively little is known, however, about the intrinsic dynamics of neurons within the KF and how their synaptic connections affect breathing pattern control and contribute to breathing irregularities. In this study, we use a reduced computational model to consider several dynamical regimes of KF activity paired with different input sources to determine which combinations are compatible with known experimental observations. We further build on these findings to identify possible interactions between the KF and other components of the respiratory neural circuitry. Specifically, we present two models that both simulate eupnoeic as well as RTT-like breathing phenotypes. Using nullcline analysis, we identify the types of inhibitory inputs to the KF leading to RTT-like respiratory patterns and suggest possible KF local circuit organizations. When the identified properties are present, the two models also exhibit quantal acceleration of late-expiratory activity, a hallmark of active expiration featuring forced exhalation, with increasing inhibition to KF, as reported experimentally. Hence, these models instantiate plausible hypotheses about possible KF dynamics and forms of local network interactions, thus providing a general framework as well as specific predictions for future experimental testing. (Figure presented.). Key points: The Kölliker–Fuse nucleus (KF), a part of the parabrachial complex, is involved in regulating normal breathing and controlling active abdominal expiration during increased ventilation. Dysfunction in KF neuronal activity is thought to contribute to respiratory abnormalities seen in Rett syndrome (RTT). This study utilizes computational modelling to explore different dynamical regimes of KF activity and their compatibility with experimental observations. By analysing different model configurations, the study identifies inhibitory inputs to the KF that lead to RTT-like respiratory patterns and proposes potential KF local circuit organizations. Two models are presented that simulate both normal breathing and RTT-like breathing patterns. These models provide testable hypotheses and specific predictions for future experimental investigations, offering a general framework for understanding KF dynamics and potential network interactions.
publishDate 2024
dc.date.none.fl_str_mv 2024-01-01
2025-04-29T20:06:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1113/JP285158
Journal of Physiology, v. 602, n. 1, p. 93-112, 2024.
1469-7793
0022-3751
https://hdl.handle.net/11449/306458
10.1113/JP285158
2-s2.0-85178966285
url http://dx.doi.org/10.1113/JP285158
https://hdl.handle.net/11449/306458
identifier_str_mv Journal of Physiology, v. 602, n. 1, p. 93-112, 2024.
1469-7793
0022-3751
10.1113/JP285158
2-s2.0-85178966285
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Physiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 93-112
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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