Evaluation of central and peripheral fatigue in the quadriceps using fractal dimension and conduction velocity in young females

PLoS One. 2015 Apr 16;10(4):e0123921. doi: 10.1371/journal.pone.0123921. eCollection 2015.

Abstract

Purpose: Over the past decade, linear and non-linear surface electromyography descriptors for central and peripheral components of fatigue have been developed. In the current study, we tested fractal dimension (FD) and conduction velocity (CV) as myoelectric descriptors of central and peripheral fatigue, respectively. To this aim, we analyzed FD and CV slopes during sustained fatiguing contractions of the quadriceps femoris in healthy humans.

Methods: A total of 29 recreationally active women (mean age±standard deviation: 24±4 years) and two female elite athletes (one power athlete, age 24 and one endurance athlete, age 30 years) performed two knee extensions: (1) at 20% maximal voluntary contraction (MVC) for 30 s, and (2) at 60% MVC held until exhaustion. Surface EMG signals were detected from the vastus lateralis and vastus medialis using bidimensional arrays.

Results: Central and peripheral fatigue were described as decreases in FD and CV, respectively. A positive correlation between FD and CV (R=0.51, p<0.01) was found during the sustained 60% MVC, probably as a result of simultaneous motor unit synchronization and a decrease in muscle fiber CV during the fatiguing task.

Conclusions: Central and peripheral fatigue can be described as changes in FD and CV, at least in young, healthy women. The significant correlation between FD and CV observed at 60% MVC suggests that a mutual interaction between central and peripheral fatigue can arise during submaximal isometric contractions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Electric Stimulation
  • Electromyography
  • Ergometry / methods
  • Female
  • Fractals
  • Humans
  • Isometric Contraction
  • Muscle Fatigue / physiology*
  • Quadriceps Muscle / physiology*
  • Signal Processing, Computer-Assisted
  • Young Adult

Grants and funding

This study was supported by the Thim van der Laan Foundation, Landquart, Switzerland (to MBP, MB, RC, and CC), and by the French Muscular Dystrophy Association (http://www.afm-telethon.com), Paris, France (grant 17191 to GD). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.