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Published on: June 15, 2018
Resistance training regulates cardiac function through modulation of miRNA-214
Stéphano Freitas Soares Melo1, Valério Garrone Barauna2, Miguel Araújo Carneiro Júnior3
1Laboratory of Biochemistry and Molecular Biology of the Exercise, School of Physical Education and Sport, University of Sao Paulo, Sao Paulo 05508-030, Brazil. stephanomelo@usp.br.
Resistance training (RT) enhances cardiac myocyte size and function by increasing SERCA2a expression, potentially via reduced miRNA-214 levels. This study explores the molecular basis of RT-induced cardiac adaptations.
Area of Science:
- Cardiovascular Physiology
- Molecular Biology
- Exercise Science
Background:
- Resistance training (RT) impacts cardiac function.
- MicroRNAs (miRNAs) play regulatory roles in cellular processes.
- SERCA2a is crucial for cardiac muscle relaxation and contraction.
Purpose of the Study:
- To investigate the effect of RT on miRNA-214 expression and its target SERCA2a in rat ventricular myocytes.
- To assess RT's influence on the morphological and mechanical properties of isolated left ventricular myocytes.
Main Methods:
- Male Wistar rats underwent an 8-week RT program (4x12 bouts/week, 80% 1RM).
- Control and trained groups were compared for myocyte dimensions and mechanical function.
- miRNA-214 and SERCA2a expression levels were quantified.
Main Results:
- RT significantly increased left ventricular myocyte width (15%) and volume (12%).
- Myocyte contraction and relaxation times were reduced post-RT.
- RT led to decreased miRNA-214 levels and increased SERCA2a expression.
Conclusions:
- RT improves cardiac myocyte dimensions and mechanical function, promoting faster contraction and relaxation.
- Enhanced SERCA2a expression, possibly due to reduced miRNA-214, underlies these adaptations.
- Epigenetic modifications via miRNA regulation may mediate RT's beneficial effects on cardiac myocytes.
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