Exploring the role of the Kölliker–Fuse nucleus in breathing variability by mathematical modelling
Main Author: | |
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Publication Date: | 2024 |
Other Authors: | , , , , |
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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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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1834482392385978368 |