Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats

Detalhes bibliográficos
Autor(a) principal: Leonardo Perin Ribeiro
Data de Publicação: 2018
Outros Autores: Leandro Ceotto Freitas Lima, Gustavo Baptista Naumann, Silvana dos Santos Meyrelles, Wellington Lunz, Simone da Fonseca Pires, Hélida Monteiro de Andrade, Juliana Brambilla Carnielli Trindade, Suely Gomes de Figueiredo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFMG
Texto Completo: https://doi.org/10.1590/1414-431X20177033
http://hdl.handle.net/1843/56289
https://orcid.org/0000-0001-9550-6095
https://orcid.org/0000-0003-0167-4093
https://orcid.org/0000-0003-2318-3340
https://orcid.org/0000-0003-2823-4530
https://orcid.org/0000-0003-2116-6379
https://orcid.org/0000-0002-5363-8329
Resumo: In the present study, we successfully demonstrated for the first time the existence of cardiac proteomic differences between non-selectively bred rats with distinct intrinsic exercise capacities. A proteomic approach based on two-dimensional gel electrophoresis coupled to mass spectrometry was used to study the left ventricle (LV) tissue proteome of rats with distinct intrinsic exercise capacity. Low running performance (LRP) and high running performance (HRP) rats were categorized by a treadmill exercise test, according to distance run to exhaustion. The running capacity of HRPs was 3.5-fold greater than LRPs. Protein profiling revealed 29 differences between HRP and LRP rats (15 proteins were identified). We detected alterations in components involved in metabolism, antioxidant and stress response, microfibrillar and cytoskeletal proteins. Contractile proteins were upregulated in the LVs of HRP rats (a-myosin heavy chain-6, myosin light chain-1 and creatine kinase), whereas the LVs of LRP rats exhibited upregulation in proteins associated with stress response (aldehyde dehydrogenase 2, a-crystallin B chain and HSPb-2). In addition, the cytoskeletal proteins desmin and a-actin were upregulated in LRPs. Taken together, our results suggest that the increased contractile protein levels in HRP rats partly accounted for their improved exercise capacity, and that proteins considered risk factors to the development of cardiovascular disease were expressed in higher amounts in LRP animals.
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spelling 2023-07-14T20:26:34Z2023-07-14T20:26:34Z2018513https://doi.org/10.1590/1414-431X201770331414-431Xhttp://hdl.handle.net/1843/56289https://orcid.org/0000-0001-9550-6095https://orcid.org/0000-0003-0167-4093https://orcid.org/0000-0003-2318-3340https://orcid.org/0000-0003-2823-4530https://orcid.org/0000-0003-2116-6379https://orcid.org/0000-0002-5363-8329In the present study, we successfully demonstrated for the first time the existence of cardiac proteomic differences between non-selectively bred rats with distinct intrinsic exercise capacities. A proteomic approach based on two-dimensional gel electrophoresis coupled to mass spectrometry was used to study the left ventricle (LV) tissue proteome of rats with distinct intrinsic exercise capacity. Low running performance (LRP) and high running performance (HRP) rats were categorized by a treadmill exercise test, according to distance run to exhaustion. The running capacity of HRPs was 3.5-fold greater than LRPs. Protein profiling revealed 29 differences between HRP and LRP rats (15 proteins were identified). We detected alterations in components involved in metabolism, antioxidant and stress response, microfibrillar and cytoskeletal proteins. Contractile proteins were upregulated in the LVs of HRP rats (a-myosin heavy chain-6, myosin light chain-1 and creatine kinase), whereas the LVs of LRP rats exhibited upregulation in proteins associated with stress response (aldehyde dehydrogenase 2, a-crystallin B chain and HSPb-2). In addition, the cytoskeletal proteins desmin and a-actin were upregulated in LRPs. Taken together, our results suggest that the increased contractile protein levels in HRP rats partly accounted for their improved exercise capacity, and that proteins considered risk factors to the development of cardiovascular disease were expressed in higher amounts in LRP animals.No presente estudo, demonstramos pela primeira vez com sucesso a existência de diferenças proteômicas cardíacas entre ratos criados de forma não seletiva com capacidades de exercício intrínsecas distintas. Uma abordagem proteômica baseada em eletroforese bidimensional em gel acoplada à espectrometria de massa foi utilizada para estudar o proteoma do tecido do ventrículo esquerdo (VE) de ratos com capacidade de exercício intrínseca distinta. Ratos de baixo desempenho na corrida (LRP) e alto desempenho na corrida (HRP) foram categorizados por um teste de exercício em esteira, de acordo com a distância percorrida até a exaustão. A capacidade de funcionamento dos HRPs foi 3,5 vezes maior do que os LRPs. O perfil de proteína revelou 29 diferenças entre ratos HRP e LRP (15 proteínas foram identificadas). Detectamos alterações em componentes envolvidos no metabolismo, resposta antioxidante e ao estresse, proteínas microfibrilares e do citoesqueleto. As proteínas contráteis foram reguladas positivamente nos LVs de ratos HRP (a-miosina cadeia pesada-6, cadeia leve de miosina-1 e creatina quinase), enquanto os LVs de ratos LRP exibiram regulação positiva em proteínas associadas à resposta ao estresse (aldeído desidrogenase 2, a- cadeia B cristalina e HSPb-2). Além disso, as proteínas do citoesqueleto desmina e a-actina foram reguladas positivamente em LRPs. Em conjunto, nossos resultados sugerem que os níveis aumentados de proteína contrátil em ratos HRP foram parcialmente responsáveis ​​por sua capacidade de exercício melhorada, e que as proteínas consideradas fatores de risco para o desenvolvimento de doenças cardiovasculares foram expressas em maiores quantidades em animais LRP.CNPq - Conselho Nacional de Desenvolvimento Científico e TecnológicoOutra AgênciaengUniversidade Federal de Minas GeraisUFMGBrasilICB - DEPARTAMENTO DE PARASITOLOGIABrazilian Journal of Medical and Biological ResearchProteômicaRatosExercício físicoEspectrometria de massasProteínasInborn aerobic capacityProteomics2-DEMSHeart proteinsCardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred ratsPadrões de expressão de proteínas cardíacas estão associados com capacidade de exercício inata distinta em ratos criados não seletivamenteinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://www.scielo.br/j/bjmbr/a/xqSWX6nMnFzKSrDXgXRGnsG/?lang=en#Leonardo Perin RibeiroLeandro Ceotto Freitas LimaGustavo Baptista NaumannSilvana dos Santos MeyrellesWellington LunzSimone da Fonseca PiresHélida Monteiro de AndradeJuliana Brambilla Carnielli TrindadeSuely Gomes de Figueiredoapplication/pdfinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGLICENSELicense.txtLicense.txttext/plain; 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dc.title.pt_BR.fl_str_mv Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
dc.title.alternative.pt_BR.fl_str_mv Padrões de expressão de proteínas cardíacas estão associados com capacidade de exercício inata distinta em ratos criados não seletivamente
title Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
spellingShingle Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
Leonardo Perin Ribeiro
Inborn aerobic capacity
Proteomics
2-DE
MS
Heart proteins
Proteômica
Ratos
Exercício físico
Espectrometria de massas
Proteínas
title_short Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
title_full Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
title_fullStr Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
title_full_unstemmed Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
title_sort Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
author Leonardo Perin Ribeiro
author_facet Leonardo Perin Ribeiro
Leandro Ceotto Freitas Lima
Gustavo Baptista Naumann
Silvana dos Santos Meyrelles
Wellington Lunz
Simone da Fonseca Pires
Hélida Monteiro de Andrade
Juliana Brambilla Carnielli Trindade
Suely Gomes de Figueiredo
author_role author
author2 Leandro Ceotto Freitas Lima
Gustavo Baptista Naumann
Silvana dos Santos Meyrelles
Wellington Lunz
Simone da Fonseca Pires
Hélida Monteiro de Andrade
Juliana Brambilla Carnielli Trindade
Suely Gomes de Figueiredo
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Leonardo Perin Ribeiro
Leandro Ceotto Freitas Lima
Gustavo Baptista Naumann
Silvana dos Santos Meyrelles
Wellington Lunz
Simone da Fonseca Pires
Hélida Monteiro de Andrade
Juliana Brambilla Carnielli Trindade
Suely Gomes de Figueiredo
dc.subject.por.fl_str_mv Inborn aerobic capacity
Proteomics
2-DE
MS
Heart proteins
topic Inborn aerobic capacity
Proteomics
2-DE
MS
Heart proteins
Proteômica
Ratos
Exercício físico
Espectrometria de massas
Proteínas
dc.subject.other.pt_BR.fl_str_mv Proteômica
Ratos
Exercício físico
Espectrometria de massas
Proteínas
description In the present study, we successfully demonstrated for the first time the existence of cardiac proteomic differences between non-selectively bred rats with distinct intrinsic exercise capacities. A proteomic approach based on two-dimensional gel electrophoresis coupled to mass spectrometry was used to study the left ventricle (LV) tissue proteome of rats with distinct intrinsic exercise capacity. Low running performance (LRP) and high running performance (HRP) rats were categorized by a treadmill exercise test, according to distance run to exhaustion. The running capacity of HRPs was 3.5-fold greater than LRPs. Protein profiling revealed 29 differences between HRP and LRP rats (15 proteins were identified). We detected alterations in components involved in metabolism, antioxidant and stress response, microfibrillar and cytoskeletal proteins. Contractile proteins were upregulated in the LVs of HRP rats (a-myosin heavy chain-6, myosin light chain-1 and creatine kinase), whereas the LVs of LRP rats exhibited upregulation in proteins associated with stress response (aldehyde dehydrogenase 2, a-crystallin B chain and HSPb-2). In addition, the cytoskeletal proteins desmin and a-actin were upregulated in LRPs. Taken together, our results suggest that the increased contractile protein levels in HRP rats partly accounted for their improved exercise capacity, and that proteins considered risk factors to the development of cardiovascular disease were expressed in higher amounts in LRP animals.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2023-07-14T20:26:34Z
dc.date.available.fl_str_mv 2023-07-14T20:26:34Z
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://hdl.handle.net/1843/56289
dc.identifier.doi.pt_BR.fl_str_mv https://doi.org/10.1590/1414-431X20177033
dc.identifier.issn.pt_BR.fl_str_mv 1414-431X
dc.identifier.orcid.pt_BR.fl_str_mv https://orcid.org/0000-0001-9550-6095
https://orcid.org/0000-0003-0167-4093
https://orcid.org/0000-0003-2318-3340
https://orcid.org/0000-0003-2823-4530
https://orcid.org/0000-0003-2116-6379
https://orcid.org/0000-0002-5363-8329
url https://doi.org/10.1590/1414-431X20177033
http://hdl.handle.net/1843/56289
https://orcid.org/0000-0001-9550-6095
https://orcid.org/0000-0003-0167-4093
https://orcid.org/0000-0003-2318-3340
https://orcid.org/0000-0003-2823-4530
https://orcid.org/0000-0003-2116-6379
https://orcid.org/0000-0002-5363-8329
identifier_str_mv 1414-431X
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Brazilian Journal of Medical and Biological Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.publisher.initials.fl_str_mv UFMG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv ICB - DEPARTAMENTO DE PARASITOLOGIA
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
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instname_str Universidade Federal de Minas Gerais (UFMG)
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reponame_str Repositório Institucional da UFMG
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