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

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...

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Autores principales: Ribeiro, L.P., Freitas-Lima, L.C., Naumann, G.B., Meyrelles, S.S., Lunz, W., Pires, S.F., Andrade, H.M., Carnielli, J.B.T., Figueiredo, S.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769761/
https://www.ncbi.nlm.nih.gov/pubmed/29340527
http://dx.doi.org/10.1590/1414-431X20177033
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author Ribeiro, L.P.
Freitas-Lima, L.C.
Naumann, G.B.
Meyrelles, S.S.
Lunz, W.
Pires, S.F.
Andrade, H.M.
Carnielli, J.B.T.
Figueiredo, S.G.
author_facet Ribeiro, L.P.
Freitas-Lima, L.C.
Naumann, G.B.
Meyrelles, S.S.
Lunz, W.
Pires, S.F.
Andrade, H.M.
Carnielli, J.B.T.
Figueiredo, S.G.
author_sort Ribeiro, L.P.
collection PubMed
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 (α-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, α-crystallin B chain and HSPβ-2). In addition, the cytoskeletal proteins desmin and α-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 pubmed-57697612018-01-31 Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats Ribeiro, L.P. Freitas-Lima, L.C. Naumann, G.B. Meyrelles, S.S. Lunz, W. Pires, S.F. Andrade, H.M. Carnielli, J.B.T. Figueiredo, S.G. Braz J Med Biol Res Research Articles 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 (α-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, α-crystallin B chain and HSPβ-2). In addition, the cytoskeletal proteins desmin and α-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. Associação Brasileira de Divulgação Científica 2018-01-11 /pmc/articles/PMC5769761/ /pubmed/29340527 http://dx.doi.org/10.1590/1414-431X20177033 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ribeiro, L.P.
Freitas-Lima, L.C.
Naumann, G.B.
Meyrelles, S.S.
Lunz, W.
Pires, S.F.
Andrade, H.M.
Carnielli, J.B.T.
Figueiredo, S.G.
Cardiac protein expression patterns are associated with distinct inborn exercise capacity in non-selectively bred rats
title 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_short 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
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769761/
https://www.ncbi.nlm.nih.gov/pubmed/29340527
http://dx.doi.org/10.1590/1414-431X20177033
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