Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats

Detalhes bibliográficos
Autor(a) principal: Carvalho, Marianna R.
Data de Publicação: 2021
Outros Autores: Mendonça, Maria Lua M., Oliveira, Jéssica M.L., Romanenghi, Rodrigo B., Morais, Camila S., Ota, Gabriel E., Lima, Aline R.R. [UNESP], Oliveira, Rodrigo J., Filiú, Wander F.O., Okoshi, Katashi [UNESP], Okoshi, Marina P. [UNESP], Oliveira-Junior, Silvio A., Martinez, Paula F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.lfs.2020.118697
http://hdl.handle.net/11449/206794
Resumo: Aim: To evaluate the influence of intermittent fasting and high-intensity interval training (HIIT) on myocardial apoptosis signaling and cardiac morphological characteristics in healthy rats. Methods: Male Wistar rats (n = 60) were divided into four groups: sedentary control (SED-C), intermittent fasting (SED-IF), high-intensity interval training (HIIT-C), and high-intensity interval training plus intermittent fasting (HIIT-IF). SED-C and HIIT-C groups were treated daily with ad libitum chow; SED-IF and HIIT-IF received the same standard chow every other day. HIIT-C and HIIT-IF rats were submitted to an HIIT protocol five times a week for 12 weeks. At the end of the experiment, functional capacity, cardiac morphology, and expression of apoptosis signaling pathways-related proteins were analyzed. Key findings: HIIT increased cardiomyocyte cross-sectional area, collagen interstitial fraction, and the pro-apoptotic proteins AIF and caspase-3 expression, and reduced pro-apoptotic protein CYTC expression and the cleaved-to-non-cleaved PARP-1 ratio in myocardium. Intermittent fasting reduced cardiomyocyte cross-sectional area, collagen interstitial fraction, and expression of Bax, CYTC and cleaved PARP-1, and increased expression of the anti-apoptotic protein BCL-2. SMAC, ARC, and caspase-8 expression was not changed by HIIT or intermittent fasting. Significance: HIIT promotes cardiomyocyte hypertrophy and interstitial fibrosis, and modulates the apoptosis signaling pathway in healthy rat myocardium. Intermittent fasting reduces pro-apoptotic and increases antiapoptotic signaling, besides attenuating HIIT-induced cardiomyocyte hypertrophy and myocardial interstitial fibrosis.
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spelling Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy ratsApoptosisHeartPhysical exerciseTime restricted feedingAim: To evaluate the influence of intermittent fasting and high-intensity interval training (HIIT) on myocardial apoptosis signaling and cardiac morphological characteristics in healthy rats. Methods: Male Wistar rats (n = 60) were divided into four groups: sedentary control (SED-C), intermittent fasting (SED-IF), high-intensity interval training (HIIT-C), and high-intensity interval training plus intermittent fasting (HIIT-IF). SED-C and HIIT-C groups were treated daily with ad libitum chow; SED-IF and HIIT-IF received the same standard chow every other day. HIIT-C and HIIT-IF rats were submitted to an HIIT protocol five times a week for 12 weeks. At the end of the experiment, functional capacity, cardiac morphology, and expression of apoptosis signaling pathways-related proteins were analyzed. Key findings: HIIT increased cardiomyocyte cross-sectional area, collagen interstitial fraction, and the pro-apoptotic proteins AIF and caspase-3 expression, and reduced pro-apoptotic protein CYTC expression and the cleaved-to-non-cleaved PARP-1 ratio in myocardium. Intermittent fasting reduced cardiomyocyte cross-sectional area, collagen interstitial fraction, and expression of Bax, CYTC and cleaved PARP-1, and increased expression of the anti-apoptotic protein BCL-2. SMAC, ARC, and caspase-8 expression was not changed by HIIT or intermittent fasting. Significance: HIIT promotes cardiomyocyte hypertrophy and interstitial fibrosis, and modulates the apoptosis signaling pathway in healthy rat myocardium. Intermittent fasting reduces pro-apoptotic and increases antiapoptotic signaling, besides attenuating HIIT-induced cardiomyocyte hypertrophy and myocardial interstitial fibrosis.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Striated Muscle Study Laboratory Federal University of Mato Grosso do Sul (UFMS)Internal Medicine Department Botucatu Medical School Sao Paulo State University (UNESP)Internal Medicine Department Botucatu Medical School Sao Paulo State University (UNESP)CAPES: 001CNPq: 482556/2013-7Universidade Federal de Mato Grosso do Sul (UFMS)Universidade Estadual Paulista (Unesp)Carvalho, Marianna R.Mendonça, Maria Lua M.Oliveira, Jéssica M.L.Romanenghi, Rodrigo B.Morais, Camila S.Ota, Gabriel E.Lima, Aline R.R. [UNESP]Oliveira, Rodrigo J.Filiú, Wander F.O.Okoshi, Katashi [UNESP]Okoshi, Marina P. [UNESP]Oliveira-Junior, Silvio A.Martinez, Paula F.2021-06-25T10:43:53Z2021-06-25T10:43:53Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.lfs.2020.118697Life Sciences, v. 264.1879-06310024-3205http://hdl.handle.net/11449/20679410.1016/j.lfs.2020.1186972-s2.0-85095578216Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLife Sciencesinfo:eu-repo/semantics/openAccess2024-08-14T17:22:26Zoai:repositorio.unesp.br:11449/206794Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:22:26Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
title Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
spellingShingle Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
Carvalho, Marianna R.
Apoptosis
Heart
Physical exercise
Time restricted feeding
title_short Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
title_full Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
title_fullStr Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
title_full_unstemmed Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
title_sort Influence of high-intensity interval training and intermittent fasting on myocardium apoptosis pathway and cardiac morphology of healthy rats
author Carvalho, Marianna R.
author_facet Carvalho, Marianna R.
Mendonça, Maria Lua M.
Oliveira, Jéssica M.L.
Romanenghi, Rodrigo B.
Morais, Camila S.
Ota, Gabriel E.
Lima, Aline R.R. [UNESP]
Oliveira, Rodrigo J.
Filiú, Wander F.O.
Okoshi, Katashi [UNESP]
Okoshi, Marina P. [UNESP]
Oliveira-Junior, Silvio A.
Martinez, Paula F.
author_role author
author2 Mendonça, Maria Lua M.
Oliveira, Jéssica M.L.
Romanenghi, Rodrigo B.
Morais, Camila S.
Ota, Gabriel E.
Lima, Aline R.R. [UNESP]
Oliveira, Rodrigo J.
Filiú, Wander F.O.
Okoshi, Katashi [UNESP]
Okoshi, Marina P. [UNESP]
Oliveira-Junior, Silvio A.
Martinez, Paula F.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Mato Grosso do Sul (UFMS)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Carvalho, Marianna R.
Mendonça, Maria Lua M.
Oliveira, Jéssica M.L.
Romanenghi, Rodrigo B.
Morais, Camila S.
Ota, Gabriel E.
Lima, Aline R.R. [UNESP]
Oliveira, Rodrigo J.
Filiú, Wander F.O.
Okoshi, Katashi [UNESP]
Okoshi, Marina P. [UNESP]
Oliveira-Junior, Silvio A.
Martinez, Paula F.
dc.subject.por.fl_str_mv Apoptosis
Heart
Physical exercise
Time restricted feeding
topic Apoptosis
Heart
Physical exercise
Time restricted feeding
description Aim: To evaluate the influence of intermittent fasting and high-intensity interval training (HIIT) on myocardial apoptosis signaling and cardiac morphological characteristics in healthy rats. Methods: Male Wistar rats (n = 60) were divided into four groups: sedentary control (SED-C), intermittent fasting (SED-IF), high-intensity interval training (HIIT-C), and high-intensity interval training plus intermittent fasting (HIIT-IF). SED-C and HIIT-C groups were treated daily with ad libitum chow; SED-IF and HIIT-IF received the same standard chow every other day. HIIT-C and HIIT-IF rats were submitted to an HIIT protocol five times a week for 12 weeks. At the end of the experiment, functional capacity, cardiac morphology, and expression of apoptosis signaling pathways-related proteins were analyzed. Key findings: HIIT increased cardiomyocyte cross-sectional area, collagen interstitial fraction, and the pro-apoptotic proteins AIF and caspase-3 expression, and reduced pro-apoptotic protein CYTC expression and the cleaved-to-non-cleaved PARP-1 ratio in myocardium. Intermittent fasting reduced cardiomyocyte cross-sectional area, collagen interstitial fraction, and expression of Bax, CYTC and cleaved PARP-1, and increased expression of the anti-apoptotic protein BCL-2. SMAC, ARC, and caspase-8 expression was not changed by HIIT or intermittent fasting. Significance: HIIT promotes cardiomyocyte hypertrophy and interstitial fibrosis, and modulates the apoptosis signaling pathway in healthy rat myocardium. Intermittent fasting reduces pro-apoptotic and increases antiapoptotic signaling, besides attenuating HIIT-induced cardiomyocyte hypertrophy and myocardial interstitial fibrosis.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:43:53Z
2021-06-25T10:43:53Z
2021-01-01
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/10.1016/j.lfs.2020.118697
Life Sciences, v. 264.
1879-0631
0024-3205
http://hdl.handle.net/11449/206794
10.1016/j.lfs.2020.118697
2-s2.0-85095578216
url http://dx.doi.org/10.1016/j.lfs.2020.118697
http://hdl.handle.net/11449/206794
identifier_str_mv Life Sciences, v. 264.
1879-0631
0024-3205
10.1016/j.lfs.2020.118697
2-s2.0-85095578216
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Life Sciences
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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
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