Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling

Detalhes bibliográficos
Autor(a) principal: Okoshi, K. [UNESP]
Data de Publicação: 2019
Outros Autores: Cezar, M. D.M. [UNESP], Polin, M. A.M. [UNESP], Paladino, J. R. [UNESP], Martinez, P. F., Oliveira, S. A., Lima, A. R.R. [UNESP], Damatto, R. L. [UNESP], Paiva, S. A.R. [UNESP], Zornoff, L. A.M. [UNESP], Okoshi, M. P. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/s12872-019-1113-4
http://hdl.handle.net/11449/189178
Resumo: Background: Information on the role of intermittent fasting (IF) on pathologic cardiac remodeling is scarce. We compared the effects of IF before and after myocardial infarction (MI) on rat cardiac remodeling and survival. Methods: Wistar rats were intermittently fasted (food available every other day) or fed ad libitum for 12 weeks and then divided into three groups: AL - fed ad libitum; AL/IF - fed AL before MI and IF after MI; and IF - fed IF before and after MI. Echocardiogram was performed before MI and 2 and 12 weeks after surgery. Isolated hearts were evaluated in Langendorff preparations. Results: Before surgery, body weight (BW) was lower in IF than AL. Final BW was lower in AL/IF and IF than AL. Perioperative mortality did not change between AL (31.3%) and IF (27.3%). Total mortality was lower in IF than AL. Before surgery, echocardiographic parameters did not differ between groups. Two weeks after surgery, MI size did not differ between groups. Twelve weeks after MI, left ventricular (LV) diastolic posterior wall thickness was lower in AL/IF and IF than AL. The percentage of variation of echocardiographic parameters between twelve and two weeks showed that MI size decreased in all groups and the reduction was higher in IF than AL/IF. In Langendorff preparations, LV volume at zero end-diastolic pressure (V0; AL: 0.41 ± 0.05; AL/IF: 0.34 ± 0.06; IF: 0.28 ± 0.05 mL) and at 25 mmHg end-diastolic pressure (V25; AL: 0.61 ± 0.05; AL/IF: 0.54 ± 0.07; IF: 0.44 ± 0.06 mL) was lower in AL/IF and IF than AL and V25 was lower in IF than AL/IF. V0/BW ratio was lower in IF than AL and LV weight/V0 ratio was higher in IF than AL. Myocyte diameter was lower in AL/IF and IF than AL (AL: 17.3 ± 1.70; AL/IF: 15.1 ± 2.21; IF: 13.4 ± 1.49 μm). Myocardial hydroxyproline concentration and gene expression of ANP, Serca 2a, and α- and β-myosin heavy chain did not differ between groups. Conclusion: Intermittent fasting initiated before or after MI reduces myocyte hypertrophy and LV dilation. Myocardial fibrosis and fetal gene expression are not modulated by feeding regimens. Benefit is more evident when intermittent fasting is initiated before rather than after MI.
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spelling Influence of intermittent fasting on myocardial infarction-induced cardiac remodelingCalorie restrictionEchocardiogramFetal gene expressionHeart failureIntermittent feedingIsolated heartLangendorff preparationMyocardial infarctionRatVentricular remodelingBackground: Information on the role of intermittent fasting (IF) on pathologic cardiac remodeling is scarce. We compared the effects of IF before and after myocardial infarction (MI) on rat cardiac remodeling and survival. Methods: Wistar rats were intermittently fasted (food available every other day) or fed ad libitum for 12 weeks and then divided into three groups: AL - fed ad libitum; AL/IF - fed AL before MI and IF after MI; and IF - fed IF before and after MI. Echocardiogram was performed before MI and 2 and 12 weeks after surgery. Isolated hearts were evaluated in Langendorff preparations. Results: Before surgery, body weight (BW) was lower in IF than AL. Final BW was lower in AL/IF and IF than AL. Perioperative mortality did not change between AL (31.3%) and IF (27.3%). Total mortality was lower in IF than AL. Before surgery, echocardiographic parameters did not differ between groups. Two weeks after surgery, MI size did not differ between groups. Twelve weeks after MI, left ventricular (LV) diastolic posterior wall thickness was lower in AL/IF and IF than AL. The percentage of variation of echocardiographic parameters between twelve and two weeks showed that MI size decreased in all groups and the reduction was higher in IF than AL/IF. In Langendorff preparations, LV volume at zero end-diastolic pressure (V0; AL: 0.41 ± 0.05; AL/IF: 0.34 ± 0.06; IF: 0.28 ± 0.05 mL) and at 25 mmHg end-diastolic pressure (V25; AL: 0.61 ± 0.05; AL/IF: 0.54 ± 0.07; IF: 0.44 ± 0.06 mL) was lower in AL/IF and IF than AL and V25 was lower in IF than AL/IF. V0/BW ratio was lower in IF than AL and LV weight/V0 ratio was higher in IF than AL. Myocyte diameter was lower in AL/IF and IF than AL (AL: 17.3 ± 1.70; AL/IF: 15.1 ± 2.21; IF: 13.4 ± 1.49 μm). Myocardial hydroxyproline concentration and gene expression of ANP, Serca 2a, and α- and β-myosin heavy chain did not differ between groups. Conclusion: Intermittent fasting initiated before or after MI reduces myocyte hypertrophy and LV dilation. Myocardial fibrosis and fetal gene expression are not modulated by feeding regimens. Benefit is more evident when intermittent fasting is initiated before rather than after MI.Internal Medicine Department Botucatu Medical School Sao Paulo State University UNESPDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Rubiao Junior, S/NItapeva Social and Agrarian Sciences College FAITFederal University of Mato Grosso Do sul Cidade Universitária, Av. Costa e Silva - PioneirosInternal Medicine Department Botucatu Medical School Sao Paulo State University UNESPDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Rubiao Junior, S/NUniversidade Estadual Paulista (Unesp)FAITCidade UniversitáriaOkoshi, K. [UNESP]Cezar, M. D.M. [UNESP]Polin, M. A.M. [UNESP]Paladino, J. R. [UNESP]Martinez, P. F.Oliveira, S. A.Lima, A. R.R. [UNESP]Damatto, R. L. [UNESP]Paiva, S. A.R. [UNESP]Zornoff, L. A.M. [UNESP]Okoshi, M. P. [UNESP]2019-10-06T16:32:21Z2019-10-06T16:32:21Z2019-05-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1186/s12872-019-1113-4BMC Cardiovascular Disorders, v. 19, n. 1, 2019.1471-2261http://hdl.handle.net/11449/18917810.1186/s12872-019-1113-42-s2.0-85066411310Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Cardiovascular Disordersinfo:eu-repo/semantics/openAccess2021-10-23T17:45:54Zoai:repositorio.unesp.br:11449/189178Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T17:45:54Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
title Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
spellingShingle Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
Okoshi, K. [UNESP]
Calorie restriction
Echocardiogram
Fetal gene expression
Heart failure
Intermittent feeding
Isolated heart
Langendorff preparation
Myocardial infarction
Rat
Ventricular remodeling
title_short Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
title_full Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
title_fullStr Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
title_full_unstemmed Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
title_sort Influence of intermittent fasting on myocardial infarction-induced cardiac remodeling
author Okoshi, K. [UNESP]
author_facet Okoshi, K. [UNESP]
Cezar, M. D.M. [UNESP]
Polin, M. A.M. [UNESP]
Paladino, J. R. [UNESP]
Martinez, P. F.
Oliveira, S. A.
Lima, A. R.R. [UNESP]
Damatto, R. L. [UNESP]
Paiva, S. A.R. [UNESP]
Zornoff, L. A.M. [UNESP]
Okoshi, M. P. [UNESP]
author_role author
author2 Cezar, M. D.M. [UNESP]
Polin, M. A.M. [UNESP]
Paladino, J. R. [UNESP]
Martinez, P. F.
Oliveira, S. A.
Lima, A. R.R. [UNESP]
Damatto, R. L. [UNESP]
Paiva, S. A.R. [UNESP]
Zornoff, L. A.M. [UNESP]
Okoshi, M. P. [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
FAIT
Cidade Universitária
dc.contributor.author.fl_str_mv Okoshi, K. [UNESP]
Cezar, M. D.M. [UNESP]
Polin, M. A.M. [UNESP]
Paladino, J. R. [UNESP]
Martinez, P. F.
Oliveira, S. A.
Lima, A. R.R. [UNESP]
Damatto, R. L. [UNESP]
Paiva, S. A.R. [UNESP]
Zornoff, L. A.M. [UNESP]
Okoshi, M. P. [UNESP]
dc.subject.por.fl_str_mv Calorie restriction
Echocardiogram
Fetal gene expression
Heart failure
Intermittent feeding
Isolated heart
Langendorff preparation
Myocardial infarction
Rat
Ventricular remodeling
topic Calorie restriction
Echocardiogram
Fetal gene expression
Heart failure
Intermittent feeding
Isolated heart
Langendorff preparation
Myocardial infarction
Rat
Ventricular remodeling
description Background: Information on the role of intermittent fasting (IF) on pathologic cardiac remodeling is scarce. We compared the effects of IF before and after myocardial infarction (MI) on rat cardiac remodeling and survival. Methods: Wistar rats were intermittently fasted (food available every other day) or fed ad libitum for 12 weeks and then divided into three groups: AL - fed ad libitum; AL/IF - fed AL before MI and IF after MI; and IF - fed IF before and after MI. Echocardiogram was performed before MI and 2 and 12 weeks after surgery. Isolated hearts were evaluated in Langendorff preparations. Results: Before surgery, body weight (BW) was lower in IF than AL. Final BW was lower in AL/IF and IF than AL. Perioperative mortality did not change between AL (31.3%) and IF (27.3%). Total mortality was lower in IF than AL. Before surgery, echocardiographic parameters did not differ between groups. Two weeks after surgery, MI size did not differ between groups. Twelve weeks after MI, left ventricular (LV) diastolic posterior wall thickness was lower in AL/IF and IF than AL. The percentage of variation of echocardiographic parameters between twelve and two weeks showed that MI size decreased in all groups and the reduction was higher in IF than AL/IF. In Langendorff preparations, LV volume at zero end-diastolic pressure (V0; AL: 0.41 ± 0.05; AL/IF: 0.34 ± 0.06; IF: 0.28 ± 0.05 mL) and at 25 mmHg end-diastolic pressure (V25; AL: 0.61 ± 0.05; AL/IF: 0.54 ± 0.07; IF: 0.44 ± 0.06 mL) was lower in AL/IF and IF than AL and V25 was lower in IF than AL/IF. V0/BW ratio was lower in IF than AL and LV weight/V0 ratio was higher in IF than AL. Myocyte diameter was lower in AL/IF and IF than AL (AL: 17.3 ± 1.70; AL/IF: 15.1 ± 2.21; IF: 13.4 ± 1.49 μm). Myocardial hydroxyproline concentration and gene expression of ANP, Serca 2a, and α- and β-myosin heavy chain did not differ between groups. Conclusion: Intermittent fasting initiated before or after MI reduces myocyte hypertrophy and LV dilation. Myocardial fibrosis and fetal gene expression are not modulated by feeding regimens. Benefit is more evident when intermittent fasting is initiated before rather than after MI.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-06T16:32:21Z
2019-10-06T16:32:21Z
2019-05-28
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/10.1186/s12872-019-1113-4
BMC Cardiovascular Disorders, v. 19, n. 1, 2019.
1471-2261
http://hdl.handle.net/11449/189178
10.1186/s12872-019-1113-4
2-s2.0-85066411310
url http://dx.doi.org/10.1186/s12872-019-1113-4
http://hdl.handle.net/11449/189178
identifier_str_mv BMC Cardiovascular Disorders, v. 19, n. 1, 2019.
1471-2261
10.1186/s12872-019-1113-4
2-s2.0-85066411310
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Cardiovascular Disorders
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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