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
Hauptverfasser: Hicks, A, Ohlendieck, K, Gopel, S. O, Pette, D
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Sprache:eng
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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.
ISSN:0363-6143
0002-9513
1522-1563
2163-5773
DOI:10.1152/ajpcell.1997.273.1.c297