Resistance training improves hemodynamic function, collagen deposition and inflammatory profiles: experimental model of heart failure

PLoS One. 2014 Oct 23;9(10):e110317. doi: 10.1371/journal.pone.0110317. eCollection 2014.

Abstract

The role of resistance training on collagen deposition, the inflammatory profile and muscle weakness in heart failure remains unclear. Therefore, this study evaluated the influence of a resistance training program on hemodynamic function, maximum strength gain, collagen deposition and inflammatory profile in chronic heart failure rats. Thirty-two male Wistar rats submitted to myocardial infarction by coronary artery ligation or sham surgery were assigned into four groups: sedentary sham (S-Sham, n = 8); trained sham (T-Sham, n = 8); sedentary chronic heart failure (S-CHF, n = 8) and trained chronic heart failure (T-CHF, n = 8). The maximum strength capacity was evaluated by the one maximum repetition test. Trained groups were submitted to an 8-week resistance training program (4 days/week, 4 sets of 10-12 repetitions/session, at 65% to 75% of one maximum repetition). After 8 weeks of the resistance training program, the T-CHF group showed lower left ventricular end diastolic pressure (P<0.001), higher left ventricular systolic pressure (P<0.05), higher systolic blood pressure (P<0.05), an improvement in the maximal positive derivative of ventricular pressure (P<0.05) and maximal negative derivative of ventricular pressure (P<0.05) when compared to the S-CHF group; no differences were observed when compared to Sham groups. In addition, resistance training was able to reduce myocardial hypertrophy (P<0.05), left ventricular total collagen volume fraction (P<0.01), IL-6 (P<0.05), and TNF-α/IL-10 ratio (P<0.05), as well as increasing IL-10 (P<0.05) in chronic heart failure rats when compared to the S-CHF group. Eight weeks of resistance training promotes an improvement of cardiac function, strength gain, collagen deposition and inflammatory profile in chronic heart failure rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure
  • Body Weight
  • Cardiomegaly / blood
  • Cardiomegaly / complications
  • Cardiomegaly / physiopathology
  • Collagen / metabolism*
  • Cytokines / blood
  • Disease Models, Animal
  • Heart Failure / blood
  • Heart Failure / complications
  • Heart Failure / physiopathology*
  • Heart Ventricles / pathology
  • Hemodynamics*
  • Inflammation / blood
  • Inflammation / complications
  • Inflammation / pathology
  • Liver / pathology
  • Lung / pathology
  • Male
  • Myocardial Infarction / blood
  • Myocardial Infarction / complications
  • Myocardial Infarction / physiopathology
  • Myocardium / metabolism
  • Myocardium / pathology
  • Rats, Wistar
  • Resistance Training*
  • Survival Analysis

Substances

  • Cytokines
  • Collagen

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.