Changes in UPR-PERK pathway and muscle hypertrophy following resistance training and creatine supplementation in rats

J Physiol Biochem. 2021 May;77(2):331-339. doi: 10.1007/s13105-021-00801-4. Epub 2021 Feb 26.

Abstract

The unfolded protein response (UPR) plays a pivotal role in some exercise training-induced physiological adaptation. Our aim was to evaluate the changes in the protein kinase R-like endoplasmic reticulum kinase (PERK) arm of the UPR and hypertrophy signaling pathway following 8 weeks of resistance training and creatine (Cr) supplementation in rats. Thirty-two adult male Wistar rats (8 weeks old) were randomly divided into 4 groups of 8: untrained + placebo (UN+P), resistance training + placebo (RT+P), untrained + Cr (UN+Cr), and resistance training + Cr (RT+Cr). Trained animals were submitted to the ladder-climbing exercise training 5 days per week for a total of 8 weeks. Cr supplementation groups received creatine diluted with 1.5 ml of 5% dextrose orally. The flexor hallucis longus (FHL) muscle was extracted 48 h after the last training session and used for western blotting. After training period, the RT+Cr and RT+P groups presented a significant increase in phosphorylated and phosphorylated/total ratio hypertrophy indices, phosphorylated and phosphorylated/total ratio PERK pathway proteins, and other downstream proteins of the PERK cascade compared with their untrained counterparts (P < 0.05). The increase in hypertrophy indices were higher but PERK pathway proteins were lower in the RT-Cr group than in the RT+P group (P < 0.05). There was no significant difference between the untrained groups (P > 0.05). Our study suggests that resistance training in addition to Cr supplementation modifies PERK pathway response and improves skeletal muscle hypertrophy.

Keywords: Creatine; Ladder-climbing training; Muscle mass; PERK pathway; UPR.

MeSH terms

  • Activating Transcription Factor 4 / genetics
  • Activating Transcription Factor 4 / metabolism
  • Adaptation, Physiological
  • Animals
  • Creatine / administration & dosage*
  • Dietary Supplements
  • Eukaryotic Initiation Factor-2 / genetics
  • Eukaryotic Initiation Factor-2 / metabolism
  • Hypertrophy / etiology
  • Hypertrophy / genetics*
  • Hypertrophy / metabolism
  • Male
  • Muscle, Skeletal / metabolism*
  • Phosphorylation
  • Physical Conditioning, Animal / methods*
  • Protein Processing, Post-Translational*
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Rats, Wistar
  • Resistance Training
  • Signal Transduction
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Transcription Factor CHOP / genetics
  • Transcription Factor CHOP / metabolism
  • Unfolded Protein Response*
  • eIF-2 Kinase / genetics*
  • eIF-2 Kinase / metabolism

Substances

  • Atf4 protein, rat
  • Ddit3 protein, rat
  • Eukaryotic Initiation Factor-2
  • Activating Transcription Factor 4
  • Transcription Factor CHOP
  • mTOR protein, rat
  • PERK kinase
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • eIF-2 Kinase
  • Creatine