Isolated quadriceps training increases maximal exercise capacity in chronic heart failure: the role of skeletal muscle convective and diffusive oxygen transport

J Am Coll Cardiol. 2011 Sep 20;58(13):1353-62. doi: 10.1016/j.jacc.2011.06.025.

Abstract

Objectives: This study sought to elucidate the mechanisms responsible for the benefits of small muscle mass exercise training in patients with chronic heart failure (CHF).

Background: How central cardiorespiratory and/or peripheral skeletal muscle factors are altered with small muscle mass training in CHF is unknown.

Methods: We studied muscle structure, and oxygen (O(2)) transport and metabolism at maximal cycle (whole-body) and knee-extensor exercise (KE) (small muscle mass) in 6 healthy controls and 6 patients with CHF who then performed 8 weeks of KE training (both legs, separately) and repeated these assessments.

Results: Pre-training cycling and KE peak leg O(2) uptake (Vo(2peak)) were ~17% and ~15% lower, respectively, in the patients compared with controls. Structurally, KE training increased quadriceps muscle capillarity and mitochondrial density by ~21% and ~25%, respectively. Functionally, despite not altering maximal cardiac output, KE training increased maximal O(2) delivery (~54%), arterial-venous O(2) difference (~10%), and muscle O(2) diffusive conductance (D(M)O(2)) (~39%) (assessed during KE), thereby increasing single-leg Vo(2peak) by ~53%, to a level exceeding that of the untrained controls. Post-training, during maximal cycling, O(2) delivery (~40%), arterial-venous O(2) difference (~15%), and D(M)O(2) (~52%) all increased, yielding an increase in Vo(2peak) of ~40%, matching the controls.

Conclusions: In the face of continued central limitations, clear improvements in muscle structure, peripheral convective and diffusive O(2) transport, and subsequently, O(2) utilization support the efficacy of local skeletal muscle training as a powerful approach to combat exercise intolerance in CHF.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport, Active
  • Biopsy
  • Blood Flow Velocity
  • Cardiac Catheterization
  • Disease Progression
  • Exercise Test
  • Exercise Tolerance / physiology*
  • Follow-Up Studies
  • Heart Failure / metabolism
  • Heart Failure / physiopathology*
  • Humans
  • Male
  • Microscopy, Electron
  • Middle Aged
  • Mitochondria, Muscle / metabolism
  • Mitochondria, Muscle / ultrastructure
  • Oxygen / metabolism*
  • Oxygen Consumption*
  • Quadriceps Muscle / metabolism
  • Quadriceps Muscle / physiopathology*
  • Quadriceps Muscle / ultrastructure
  • Severity of Illness Index
  • Stroke Volume

Substances

  • Oxygen