PeerJ (Apr 2021)

Transcriptional profile in rat muscle: down-regulation networks in acute strenuous exercise

  • Stela Mirla da Silva Felipe,
  • Raquel Martins de Freitas,
  • Emanuel Diego dos Santos Penha,
  • Christina Pacheco,
  • Danilo Lopes Martins,
  • Juliana Osório Alves,
  • Paula Matias Soares,
  • Adriano César Carneiro Loureiro,
  • Tanes Lima,
  • Leonardo R. Silveira,
  • Alex Soares Marreiros Ferraz,
  • Jorge Estefano Santana de Souza,
  • Jose Henrique Leal-Cardoso,
  • Denise P. Carvalho,
  • Vania Marilande Ceccatto

DOI
https://doi.org/10.7717/peerj.10500
Journal volume & issue
Vol. 9
p. e10500

Abstract

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Background Physical exercise is a health promotion factor regulating gene expression and causing changes in phenotype, varying according to exercise type and intensity. Acute strenuous exercise in sedentary individuals appears to induce different transcriptional networks in response to stress caused by exercise. The objective of this research was to investigate the transcriptional profile of strenuous experimental exercise. Methodology RNA-Seq was performed with Rattus norvegicus soleus muscle, submitted to strenuous physical exercise on a treadmill with an initial velocity of 0.5 km/h and increments of 0.2 km/h at every 3 min until animal exhaustion. Twenty four hours post-physical exercise, RNA-seq protocols were performed with coverage of 30 million reads per sample, 100 pb read length, paired-end, with a list of counts totaling 12816 genes. Results Eighty differentially expressed genes (61 down-regulated and 19 up-regulated) were obtained. Reactome and KEGG database searches revealed the most significant pathways, for down-regulated gene set, were: PI3K-Akt signaling pathway, RAF-MAP kinase, P2Y receptors and Signaling by Erbb2. Results suggest PI3K-AKT pathway inactivation by Hbegf, Fgf1 and Fgr3 receptor regulation, leading to inhibition of cell proliferation and increased apoptosis. Cell signaling transcription networks were found in transcriptome. Results suggest some metabolic pathways which indicate the conditioning situation of strenuous exercise induced genes encoding apoptotic and autophagy factors, indicating cellular stress. Conclusion Down-regulated networks showed cell transduction and signaling pathways, with possible inhibition of cellular proliferation and cell degeneration. These findings reveal transitory and dynamic process in cell signaling transcription networks in skeletal muscle after acute strenuous exercise.

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