Early functional and biochemical adaptations to low-frequency stimulation of rabbit fast-twitch muscle
A. Hicks, K. Ohlendieck, S. O. Gopel and D. Pette Faculty of Biology, University of Konstanz, Germany. To examine mechanisms underlying force reduction after the onset of chronic low-frequency (10 Hz) stimulation (CLFS), we exposed rabbit tibialis anterior muscles to various durations of CLFS. To fo...
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Veröffentlicht in: | American Journal of Physiology: Cell Physiology 1997-07, Vol.273 (1), p.C297-C305 |
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Zusammenfassung: | A. Hicks, K. Ohlendieck, S. O. Gopel and D. Pette
Faculty of Biology, University of Konstanz, Germany.
To examine mechanisms underlying force reduction after the onset of chronic
low-frequency (10 Hz) stimulation (CLFS), we exposed rabbit tibialis
anterior muscles to various durations of CLFS. To follow changes in
isometric contractile properties and electromyographic (EMG) activity, we
studied stimulated and contralateral muscles during a terminal test at 10
Hz for 10 min. In addition, activities and protein amounts of the
sarcoplasmic reticulum Ca(2+)-ATPase, content of Na(+)-K(+)-ATPase, and
expression patterns of triad junction components were examined. Force
output and EMG amplitude declined abruptly soon after the onset of
stimulation, suggesting refractoriness of a large fiber population.
Although twitch force and to a lesser extent EMG activity gradually
recovered after stimulation for 6 days and longer, the muscles exhibited
profoundly altered properties, i.e., enhanced fatigue resistance, absence
of twitch potentiation, and prolonged contraction and relaxation times.
These changes were associated with significant increases in
Na(+)-K(+)-ATPase concentration and significant decreases in Ca(2+)-ATPase,
ryanodine receptor, dihydropyridine receptor, and triadin concentrations
over the course of the 20 days of stimulation. Alterations in excitability,
Ca2+ handling, and excitation-contraction coupling prior to changes in
myofibrillar protein isoforms may thus be responsible for early functional
alterations. |
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ISSN: | 0363-6143 0002-9513 1522-1563 2163-5773 |
DOI: | 10.1152/ajpcell.1997.273.1.c297 |