Frog skeletal muscle fibers recovering from fatigue have reduced charge movement

Joseph D. Bruton, Péter Szentesi, Jan Lännergren, Håkan Westerblad, László Kovács, László Csernoch

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Abstract

Following prolonged exercise, muscle force production is often impaired. One possible cause of this force deficit is impaired intracellular activation. We have used single skeletal muscle fibers from the lumbrical muscle of Xenopus laevis to study the effects of fatigue on excitation-contraction coupling. Fatigue was induced in 13 intact fibers. Five fibers recovered in normal Ringer only (fatigued-only fibers). The remaining eight fibers were subjected to a brief hypotonic treatment (F-H fibers) that is known to prolong the effects of fatigue. Intramembrane charge movement, changes in intracellular calcium concentration ([Ca2+]i) and force transients were measured in a single Vaseline gap chamber under voltage clamp. In F-H fibers, membrane capacitance was reduced. Confocal microscopy showed that this was not due to closure of the transverse tubules. The amount of normalized intramembrane charge was reduced from 21.0 ± 2.8 nC/μF (n = 10) in rested fibers to 12.2 ± 1.1 nC/μF in F-H fibers. However, the voltage dependence of intramembrane charge movement was unchanged. In F-H fibers, force production was virtually abolished. This was the consequence of the greatly reduced [Ca2+]i accompanying a depolarizing pulse. In recovering fatigued-only fibers, while the maximal available charge was not significantly smaller (18.3 ± 1.1 nC/μF), both calcium and force were reduced, albeit to a lesser extent than in F-H fibers. The data are consistent with a model where fatigue reduces the number of voltage sensors in the t-tubules and, in addition, alters the coupling between the remaining functional voltage sensors and the calcium channels of the sarcoplasmic reticulum.

Original languageEnglish
Pages (from-to)621-628
Number of pages8
JournalJournal of Muscle Research and Cell Motility
Volume21
Issue number7
DOIs
Publication statusPublished - Dec 1 2000

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ASJC Scopus subject areas

  • Biochemistry
  • Physiology
  • Cell Biology

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