Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats

Detalhes bibliográficos
Autor(a) principal: Moraes, Davi José de Almeida
Data de Publicação: 2014
Outros Autores: Bonagamba, Leni Gomes Heck, Costa, Kauê Machado, Costa-Silva, João Henrique, Zoccal, Daniel Breseghello [UNESP], Machado, Benedito Honório
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://onlinelibrary.wiley.com/doi/10.1113/jphysiol.2013.262212/abstract?systemMessage=Wiley+Online+Library+will+have+intermittent+access+on+8th+August+2015+from+10%3A00-16%3A00+BST+%2F+05%3A00-11%3A00+EDT+%2F+17%3A00-23%3A00+SGT+for+essential+maintenance.++Apologies+for+the+inconvenience.
http://hdl.handle.net/11449/125705
Resumo: Individuals experiencing sustained hypoxia (SH) exhibit adjustments in the respiratory and autonomic functions by neural mechanisms not yet elucidated. In the present study we evaluated the central mechanisms underpinning the SH-induced changes in the respiratory pattern and their impact on the sympathetic outflow. Using a decerebrated arterially perfused in situ preparation, we verified that juvenile rats exposed to SH (10% O2) for 24 h presented an active expiratory pattern, with increased abdominal, hypoglossal and vagal activities during late-expiration (late-E). SH also enhanced the activity of augmenting-expiratory neurones and depressed the activity of post-inspiratory neurones of the Botzinger complex (B ¨ otC) ¨ by mechanisms not related to changes in their intrinsic electrophysiological properties. SH rats exhibited high thoracic sympathetic activity and arterial pressure levels associated with an augmented firing frequency of pre-sympathetic neurones of the rostral ventrolateral medulla (RVLM) during the late-E phase. The antagonism of ionotropic glutamatergic receptors in the BotC/RVLM abolished the late-E bursts in expiratory and sympathetic outputs of SH rats, ¨ indicating that glutamatergic inputs to the BotC/RVLM are essential for the changes in the ¨ expiratory and sympathetic coupling observed in SH rats. We also observed that the usually silent late-E neurones of the retrotrapezoid nucleus/parafacial respiratory group became active in SH rats, suggesting that this neuronal population may provide the excitatory drive essential to the emergence of active expiration and sympathetic overactivity. We conclude that short-term SH induces the activation of medullary expiratory neurones, which affects the pattern of expiratory motor activity and its coupling with sympathetic activity.
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spelling Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in ratsIndividuals experiencing sustained hypoxia (SH) exhibit adjustments in the respiratory and autonomic functions by neural mechanisms not yet elucidated. In the present study we evaluated the central mechanisms underpinning the SH-induced changes in the respiratory pattern and their impact on the sympathetic outflow. Using a decerebrated arterially perfused in situ preparation, we verified that juvenile rats exposed to SH (10% O2) for 24 h presented an active expiratory pattern, with increased abdominal, hypoglossal and vagal activities during late-expiration (late-E). SH also enhanced the activity of augmenting-expiratory neurones and depressed the activity of post-inspiratory neurones of the Botzinger complex (B ¨ otC) ¨ by mechanisms not related to changes in their intrinsic electrophysiological properties. SH rats exhibited high thoracic sympathetic activity and arterial pressure levels associated with an augmented firing frequency of pre-sympathetic neurones of the rostral ventrolateral medulla (RVLM) during the late-E phase. The antagonism of ionotropic glutamatergic receptors in the BotC/RVLM abolished the late-E bursts in expiratory and sympathetic outputs of SH rats, ¨ indicating that glutamatergic inputs to the BotC/RVLM are essential for the changes in the ¨ expiratory and sympathetic coupling observed in SH rats. We also observed that the usually silent late-E neurones of the retrotrapezoid nucleus/parafacial respiratory group became active in SH rats, suggesting that this neuronal population may provide the excitatory drive essential to the emergence of active expiration and sympathetic overactivity. We conclude that short-term SH induces the activation of medullary expiratory neurones, which affects the pattern of expiratory motor activity and its coupling with sympathetic activity.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Universidade de São Paulo, Departamento de Fisiologia, Faculdade de Medicina de Ribeirão PretoUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Fisiologia e Patologia, Faculdade de Odontologia de AraraquaraFAPESP: 2006/51159-6FAPESP: 2009/50113-0CNPq: 502098/2008-2CNPq: 301147/2008-6Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Moraes, Davi José de AlmeidaBonagamba, Leni Gomes HeckCosta, Kauê MachadoCosta-Silva, João HenriqueZoccal, Daniel Breseghello [UNESP]Machado, Benedito Honório2015-08-06T16:12:53Z2015-08-06T16:12:53Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2013-2033application/pdfhttp://onlinelibrary.wiley.com/doi/10.1113/jphysiol.2013.262212/abstract?systemMessage=Wiley+Online+Library+will+have+intermittent+access+on+8th+August+2015+from+10%3A00-16%3A00+BST+%2F+05%3A00-11%3A00+EDT+%2F+17%3A00-23%3A00+SGT+for+essential+maintenance.++Apologies+for+the+inconvenience.Journal of Physiology, v. 592, n. 9, p. 2013-2033, 2014.0022-3751http://hdl.handle.net/11449/12570510.1113/jphysiol.2013.262212ISSN0022-3751-2014-592-09-2013-2033.pdf191291111394249706175161885539541958567557189244Currículo Lattesreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Physiology4.5402,051info:eu-repo/semantics/openAccess2024-01-23T07:07:04Zoai:repositorio.unesp.br:11449/125705Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:45:34.939123Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
title Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
spellingShingle Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
Moraes, Davi José de Almeida
title_short Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
title_full Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
title_fullStr Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
title_full_unstemmed Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
title_sort Short-term sustained hypoxia induces changes in the coupling of sympathetic and respiratory activities in rats
author Moraes, Davi José de Almeida
author_facet Moraes, Davi José de Almeida
Bonagamba, Leni Gomes Heck
Costa, Kauê Machado
Costa-Silva, João Henrique
Zoccal, Daniel Breseghello [UNESP]
Machado, Benedito Honório
author_role author
author2 Bonagamba, Leni Gomes Heck
Costa, Kauê Machado
Costa-Silva, João Henrique
Zoccal, Daniel Breseghello [UNESP]
Machado, Benedito Honório
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Moraes, Davi José de Almeida
Bonagamba, Leni Gomes Heck
Costa, Kauê Machado
Costa-Silva, João Henrique
Zoccal, Daniel Breseghello [UNESP]
Machado, Benedito Honório
description Individuals experiencing sustained hypoxia (SH) exhibit adjustments in the respiratory and autonomic functions by neural mechanisms not yet elucidated. In the present study we evaluated the central mechanisms underpinning the SH-induced changes in the respiratory pattern and their impact on the sympathetic outflow. Using a decerebrated arterially perfused in situ preparation, we verified that juvenile rats exposed to SH (10% O2) for 24 h presented an active expiratory pattern, with increased abdominal, hypoglossal and vagal activities during late-expiration (late-E). SH also enhanced the activity of augmenting-expiratory neurones and depressed the activity of post-inspiratory neurones of the Botzinger complex (B ¨ otC) ¨ by mechanisms not related to changes in their intrinsic electrophysiological properties. SH rats exhibited high thoracic sympathetic activity and arterial pressure levels associated with an augmented firing frequency of pre-sympathetic neurones of the rostral ventrolateral medulla (RVLM) during the late-E phase. The antagonism of ionotropic glutamatergic receptors in the BotC/RVLM abolished the late-E bursts in expiratory and sympathetic outputs of SH rats, ¨ indicating that glutamatergic inputs to the BotC/RVLM are essential for the changes in the ¨ expiratory and sympathetic coupling observed in SH rats. We also observed that the usually silent late-E neurones of the retrotrapezoid nucleus/parafacial respiratory group became active in SH rats, suggesting that this neuronal population may provide the excitatory drive essential to the emergence of active expiration and sympathetic overactivity. We conclude that short-term SH induces the activation of medullary expiratory neurones, which affects the pattern of expiratory motor activity and its coupling with sympathetic activity.
publishDate 2014
dc.date.none.fl_str_mv 2014
2015-08-06T16:12:53Z
2015-08-06T16:12:53Z
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://onlinelibrary.wiley.com/doi/10.1113/jphysiol.2013.262212/abstract?systemMessage=Wiley+Online+Library+will+have+intermittent+access+on+8th+August+2015+from+10%3A00-16%3A00+BST+%2F+05%3A00-11%3A00+EDT+%2F+17%3A00-23%3A00+SGT+for+essential+maintenance.++Apologies+for+the+inconvenience.
Journal of Physiology, v. 592, n. 9, p. 2013-2033, 2014.
0022-3751
http://hdl.handle.net/11449/125705
10.1113/jphysiol.2013.262212
ISSN0022-3751-2014-592-09-2013-2033.pdf
1912911113942497
0617516188553954
1958567557189244
url http://onlinelibrary.wiley.com/doi/10.1113/jphysiol.2013.262212/abstract?systemMessage=Wiley+Online+Library+will+have+intermittent+access+on+8th+August+2015+from+10%3A00-16%3A00+BST+%2F+05%3A00-11%3A00+EDT+%2F+17%3A00-23%3A00+SGT+for+essential+maintenance.++Apologies+for+the+inconvenience.
http://hdl.handle.net/11449/125705
identifier_str_mv Journal of Physiology, v. 592, n. 9, p. 2013-2033, 2014.
0022-3751
10.1113/jphysiol.2013.262212
ISSN0022-3751-2014-592-09-2013-2033.pdf
1912911113942497
0617516188553954
1958567557189244
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Physiology
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dc.format.none.fl_str_mv 2013-2033
application/pdf
dc.source.none.fl_str_mv Currículo Lattes
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)
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