| Literature DB >> 1527221 |
M C Garcia1, A F Diaz, R Godinez, J A Sanchez.
Abstract
Measurements of isometric tension were performed in single twitch skeletal muscle fibres and the effect of extracellular Na+ removal on contraction was investigated. Na+ withdrawal brought about an increase in the amplitude of K+ contractures and their time course became faster. The potentiation of K+ contractures depended strongly on extracellular Ca2+ and developed slowly following an exponential time course with a time constant of approximately 8 min. Removal of extracellular Na+ greatly increased the amplitude of caffeine contractures and lowered its threshold: caffeine (0.5 mM) had no effect on resting tension in Ringer's but produced contractures in Na(+)-free solutions. Intramembrane charge movement (charge 1) was monitored in contracting voltage-clamped segments of frog skeletal muscle fibres using the triple-Vaseline-gap technique. Movement of charge 1 did not depend on the presence of extracellular Na+. However, the mechanical threshold decreased by approximately 10 mV at several pulse durations and the charge which produced just detectable contractions decreased by approximately 5 nC microF-1 in the absence of extracellular Na+. Intracellular heparin (40 mg ml-1) increased the mechanical threshold by approximately 20 mV without affecting the movement of charge 1. The effect of Na(+)-free solutions on the mechanical threshold was additive to that of heparin. It is concluded that the effects of Na(+)-withdrawal on contraction take place at a location beyond the voltage sensor of excitation-contraction coupling.Entities:
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Year: 1992 PMID: 1527221 DOI: 10.1007/bf01766463
Source DB: PubMed Journal: J Muscle Res Cell Motil ISSN: 0142-4319 Impact factor: 2.698