Force enhancement and relaxation rates after stretch of activated muscle fibres

Proc Biol Sci. 2005 Mar 7;272(1562):475-80. doi: 10.1098/rspb.2004.2967.

Abstract

The residual force enhancement following muscle stretch might be associated with an increase in the proportion of attached cross-bridges, as supported by stiffness measurements. In this case, it could be caused by an increase in the attachment or a decrease in the detachment rate of cross-bridges, or a combination of the two. The purpose of this study was to investigate if the stretch-induced force enhancement is related to cross-bridge attachment/detachment kinetics. Single muscle fibres dissected from the lumbrical muscle of frog were place at a length approximately 20% longer than the plateau of the force-length relationship; they were maximally activated, and after full isometric force was reached, ramp stretches were imposed with amplitudes of 5 and 10% fibre length, at a speed of 40% fibre length s(-1). Experiments were performed in Ringer's solution, and with the addition of 2, 5 and 10 nM of 2,3-butanedione monoxime (BDM), a drug that places cross-bridges in a pre-power-stroke, state, inhibiting force production. The total force following stretch was higher than the corresponding force measured after isometric contraction at the corresponding length. This residual force enhancement was accompanied by an increase relaxation time. BDM, which decreases force production during isometric contractions, considerably increased the relative levels of force enhancement. BDM also increased relaxation times after stretch, beyond the levels observed during reference contractions in Ringer's solution, and beyond isometric control tests at the corresponding BDM concentrations. Together, these results support the idea that force enhancement is caused, at least in part, by a decrease in cross-bridge detachment rates, as manifested by the increased relaxation times following fibre stretch.

Publication types

  • Comparative Study

MeSH terms

  • Analysis of Variance
  • Animals
  • Biomechanical Phenomena
  • Diacetyl / analogs & derivatives*
  • Diacetyl / pharmacology
  • Isometric Contraction / drug effects
  • Isometric Contraction / physiology*
  • Kinetics
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / physiology*
  • Muscle Relaxation / drug effects
  • Muscle Relaxation / physiology*
  • Rana pipiens

Substances

  • diacetylmonoxime
  • Diacetyl