Resistance Training Regulates Cardiac Function through Modulation of miRNA-214

Aims: To determine the effects of resistance training (RT) on the expression of microRNA (miRNA)-214 and its target in sarcoplasmic reticulum Ca2+-ATPase (SERCA2a), and on the morphological and mechanical properties of isolated left ventricular myocytes. Main methods: Male Wistar rats were divided...

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Main Authors: Stéphano Freitas Soares Melo, Valério Garrone Barauna, Miguel Araújo Carneiro Júnior, Luiz Henrique Marchesi Bozi, Lucas Rios Drummond, Antônio José Natali, Edilamar Menezes de Oliveira
Format: Article
Language:English
Published: MDPI AG 2015-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/16/4/6855
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spelling doaj-f51c5a6eb34a47adb82d81adfbdae0742020-11-25T01:44:55ZengMDPI AGInternational Journal of Molecular Sciences1422-00672015-03-011646855686710.3390/ijms16046855ijms16046855Resistance Training Regulates Cardiac Function through Modulation of miRNA-214Stéphano Freitas Soares Melo0Valério Garrone Barauna1Miguel Araújo Carneiro Júnior2Luiz Henrique Marchesi Bozi3Lucas Rios Drummond4Antônio José Natali5Edilamar Menezes de Oliveira6Laboratory of Biochemistry and Molecular Biology of the Exercise, School of Physical Education and Sport, University of Sao Paulo, Sao Paulo 05508-030, BrazilLaboratory of Molecular Physiology, Health Sciences Center, Federal University of Espírito Santo, Vitória 29043-900, BrazilDepartment of Physical Education, Federal University of Viçosa, Viçosa, Minas Gerais 36570-900, BrazilLaboratory of Biochemistry and Molecular Biology of the Exercise, School of Physical Education and Sport, University of Sao Paulo, Sao Paulo 05508-030, BrazilDepartment of Physical Education, Federal University of Viçosa, Viçosa, Minas Gerais 36570-900, BrazilDepartment of Physical Education, Federal University of Viçosa, Viçosa, Minas Gerais 36570-900, BrazilLaboratory of Biochemistry and Molecular Biology of the Exercise, School of Physical Education and Sport, University of Sao Paulo, Sao Paulo 05508-030, BrazilAims: To determine the effects of resistance training (RT) on the expression of microRNA (miRNA)-214 and its target in sarcoplasmic reticulum Ca2+-ATPase (SERCA2a), and on the morphological and mechanical properties of isolated left ventricular myocytes. Main methods: Male Wistar rats were divided into two groups (n = 7/group): Control (CO) or trained (TR). The exercise-training protocol consisted of: 4 × 12 bouts, 5×/week during 8 weeks, with 80% of one repetition maximum. Key findings: RT increased the left ventricular myocyte width by 15% and volume by 12%, compared with control animals (p < 0.05). The time to half relaxation and time to peak were 8.4% and 4.4% lower, respectively, in cells from TR group as compared to CO group (p < 0.05). RT decreased miRNA-214 level by 18.5% while its target SERCA2a expression were 18.5% higher (p < 0.05). Significance: Our findings showed that RT increases single left ventricular myocyte dimensions and also leads to faster cell contraction and relaxation. These mechanical adaptations may be related to the augmented expression of SERCA2a which, in turn, may be associated with the epigenetic modification of decreased miRNA-214 expression.http://www.mdpi.com/1422-0067/16/4/6855resistance trainingcardiovascularmicroRNAcardiomyocytes
collection DOAJ
language English
format Article
sources DOAJ
author Stéphano Freitas Soares Melo
Valério Garrone Barauna
Miguel Araújo Carneiro Júnior
Luiz Henrique Marchesi Bozi
Lucas Rios Drummond
Antônio José Natali
Edilamar Menezes de Oliveira
spellingShingle Stéphano Freitas Soares Melo
Valério Garrone Barauna
Miguel Araújo Carneiro Júnior
Luiz Henrique Marchesi Bozi
Lucas Rios Drummond
Antônio José Natali
Edilamar Menezes de Oliveira
Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
International Journal of Molecular Sciences
resistance training
cardiovascular
microRNA
cardiomyocytes
author_facet Stéphano Freitas Soares Melo
Valério Garrone Barauna
Miguel Araújo Carneiro Júnior
Luiz Henrique Marchesi Bozi
Lucas Rios Drummond
Antônio José Natali
Edilamar Menezes de Oliveira
author_sort Stéphano Freitas Soares Melo
title Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
title_short Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
title_full Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
title_fullStr Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
title_full_unstemmed Resistance Training Regulates Cardiac Function through Modulation of miRNA-214
title_sort resistance training regulates cardiac function through modulation of mirna-214
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2015-03-01
description Aims: To determine the effects of resistance training (RT) on the expression of microRNA (miRNA)-214 and its target in sarcoplasmic reticulum Ca2+-ATPase (SERCA2a), and on the morphological and mechanical properties of isolated left ventricular myocytes. Main methods: Male Wistar rats were divided into two groups (n = 7/group): Control (CO) or trained (TR). The exercise-training protocol consisted of: 4 × 12 bouts, 5×/week during 8 weeks, with 80% of one repetition maximum. Key findings: RT increased the left ventricular myocyte width by 15% and volume by 12%, compared with control animals (p < 0.05). The time to half relaxation and time to peak were 8.4% and 4.4% lower, respectively, in cells from TR group as compared to CO group (p < 0.05). RT decreased miRNA-214 level by 18.5% while its target SERCA2a expression were 18.5% higher (p < 0.05). Significance: Our findings showed that RT increases single left ventricular myocyte dimensions and also leads to faster cell contraction and relaxation. These mechanical adaptations may be related to the augmented expression of SERCA2a which, in turn, may be associated with the epigenetic modification of decreased miRNA-214 expression.
topic resistance training
cardiovascular
microRNA
cardiomyocytes
url http://www.mdpi.com/1422-0067/16/4/6855
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