期刊
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
卷 88, 期 10, 页码 937-948出版社
CANADIAN SCIENCE PUBLISHING
DOI: 10.1139/Y10-068
关键词
skeletal muscle; intact frog fibres; activation; cross-bridge model; velocity
资金
- Alberta Heritage Foundation for Medical Research
- Canada Research Chairs Program
- Natural Sciences and Engineering Research Council of Canada
- Canada Foundation for Innovation
The maximal shortening velocity of a muscle (V-max) provides a link between its macroscopic properties and the underlying biochemical reactions and is altered in some diseases. Two methods that are widely used for determining V-max are afterloaded and isotonic release contractions. To determine whether these two methods give equivalent results, we calculated V-max in 9 intact single fibres from the lumbrical muscles of the frog Xenopus laevis 99.5-15.5 degrees C, stimulation frequency 35-70 Hz). The data were modelled using a 3-state cross-bridge model in which the states were inactive, detached, and attached. Afterloaded contractions gave lower predictions of V-max than did isotonic release contractions in all 9 fibres (3.20 +/- 0.84 versus 4.11 +/- 1.08 lengths per second, respectively; means +/- SD, p = 0.001) and underestimated unloaded shortening velocity measured with the slack test by an average of 29% (p = 0.001, n = 6). Excellent model predictions could be obtained by assuming that activation is inhibited by shortening. We conclude that under the experimental conditions used in this study, afterloaded and isotonic release contractions do not give equivalent results. When a change in the V-max measured with afterloaded contractions is observed in diseased muscle, it is important to consider that this may reflect differences in either activation kinetics or cross-bridge cycling rates.
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