Resistance training and L-arginine supplementation are determinant in genomic stability, cardiac contractility and muscle mass development in rats

PLoS One. 2018 Sep 27;13(9):e0204858. doi: 10.1371/journal.pone.0204858. eCollection 2018.

Abstract

L-arginine supplementation has been related to increased maximum strength and improvement of hemodynamic parameters in several diseases. The aim of our study was to evaluate the effect of L-arginine supplementation and resistance training on muscle mass, hemodynamic function and DNA damage in healthy rats subjected to a low-arginine concentration diet. Twenty three Wistar rats (290-320g) were divided into 4 groups: Sedentary (SED-Arg, n = 6), Sedentary+Arg (SED+Arg, n = 6), Resistance Training (RT-Arg, n = 5), Resistance Training+Arg (RT+Arg, n = 6). Trained animals performed resistance training protocol in a squat apparatus adapted for rats (4 sets of 10-12 repetitions, 90s of interval, 4x/week, 65-75% of One Maximum Repetition, for 8 weeks). Comet assay was performed to measure DNA damage in leukocytes. The resistance training induced higher muscle mass in trained groups. The L-arginine supplementation increased both gastrocnemius and left ventricle to body mass ratio and increased left ventricle contractility without changing hemodynamic variables. The SED+Arg group showed higher concentration of extracellular heat shock protein 72 (eHSP72) and total testosterone, as well as lower uric acid concentration in blood versus SED-Arg group. The administration of isolated L-arginine supplementation and its association with resistance training promoted less damage in leukocytes DNA. In conclusion, the L-arginine supplementation showed synergistic effect with resistance training regarding leukocyte genomic stability in a low-L-arginine diet scenario.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / pharmacology*
  • DNA Damage
  • Dietary Supplements*
  • Genomic Instability / drug effects*
  • Leukocytes / metabolism
  • Male
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • Myocardial Contraction / drug effects*
  • Organ Size / drug effects
  • Physical Conditioning, Animal*
  • Rats
  • Rats, Wistar

Substances

  • Arginine

Grants and funding

This work was supported by grants from the following: CAPES and CNPq, Brasília, Brazil, and PROAP/UFCSPA, Porto Alegre, Brazil (http://www.capes.gov.br/; http://www.ufcspa.edu.br/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.