Experimental muscle pain reduces initial motor unit discharge rates during sustained submaximal contractions

J Appl Physiol (1985). 2005 Mar;98(3):999-1005. doi: 10.1152/japplphysiol.01059.2004. Epub 2004 Oct 29.

Abstract

The aim of this human study was to investigate the effect of experimentally induced muscle pain on the modifications of motor unit discharge rate during sustained, constant-force contractions. Intramuscular and multichannel surface electromyographic (EMG) signals were collected from the right and left tibialis anterior muscle of 11 volunteers. The subjects performed two 4-min-long isometric contractions at 25% of the maximal dorsiflexion torque, separated by a 20-min rest. Before the beginning of the second contraction, hypertonic (painful; right leg) or isotonic (nonpainful; left leg) saline was injected into the tibialis anterior. Pain intensity scores did not change significantly in the first 150 s of the painful contraction. Exerted torque and its coefficient of variation were the same for the painful and nonpainful contractions. Motor unit discharge rate was higher in the beginning of the nonpainful contraction than the painful contraction on the right side [means +/- SE, 11.3 +/- 0.2 vs. 10.6 +/- 0.2 pulses/s (pps); P < 0.01] whereas it was the same for the two contractions on the left side (11.6 +/- 0.2 vs. 11.5 +/- 0.2 pps). The decrease in discharge rate in 4 min was smaller for the painful (0.4 +/- 0.1 pps) than for the control contractions (1.3 +/- 0.1 pps). Initial value and decrease in motor unit conduction velocity were not different in the four contractions (right leg, 4.0 +/- 0.1 m/s with decrease of 0.6 +/- 0.1 m/s in 4 min; left leg, 4.1 +/- 0.1 m/s with 0.7 +/- 0.1 m/s decrease). In conclusion, stimulation of nociceptive afferents by injection of hypertonic saline did not alter motor unit conduction velocity but reduced the initial motor unit discharge rates and the difference between initial and final discharge rates during sustained contraction.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Electromyography / drug effects
  • Electromyography / methods*
  • Female
  • Humans
  • Isometric Contraction*
  • Male
  • Motor Neurons*
  • Muscle Fibers, Skeletal*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / physiopathology*
  • Myofascial Pain Syndromes / chemically induced
  • Myofascial Pain Syndromes / physiopathology*
  • Physical Endurance*
  • Physical Stimulation / methods
  • Saline Solution, Hypertonic

Substances

  • Saline Solution, Hypertonic