MECHANISMS RESISTING FATIGUE IN ISOMETRICALLY CONTRACTING HUMAN SKELETAL MUSCLE
Human adductor pollicis was fatigued during circulatory occlusion by supramaximal stimulation via the ulnar nerve using intermittent trains of stimuli in ascending (1, 10, 20, 50 and 100 Hz) and descending (100, 50, 20, 10 and 1 Hz) frequencies to investigate the contribution of relaxation rate slow...
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Veröffentlicht in: | Experimental physiology 1988-11, Vol.73 (6), p.903-914 |
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Zusammenfassung: | Human adductor pollicis was fatigued during circulatory occlusion by supramaximal stimulation via the ulnar nerve using intermittent
trains of stimuli in ascending (1, 10, 20, 50 and 100 Hz) and descending (100, 50, 20, 10 and 1 Hz) frequencies to investigate
the contribution of relaxation rate slowing and post-tetanic potentiation (PTP) to fatigue resistance. At 50 and 100 Hz force
was initially well maintained despite a marked loss of excitation as indicated by EMG, demonstrating the operation of a high-frequency
âsafety factorâ which appeared independent of the pattern of stimulation. At 10 Hz, force was initially potentiated before
declining during both activity series. Potentiation was greater during the descending frequency series and the rate of decline
of force, or fatigability, was reduced. The âextraâ low-frequency potentiation at 10 Hz was not simply the result of PTP of
twitch force, since this declined more during the descending than during the ascending series, nor the result of maximal relaxation
rate changes which were identical for both fatiguing series. It is hypothesized that the extra potentiation and reduced fatigability
at low stimulation frequencies, when preceded by high frequency, is the result of increased myofibrillar Ca 2+ availability and/or sensitivity. These findings may have important practical implications in relation to functional electrical
stimulation techniques as used in paraplegia and in other areas of muscle research where fatigue is to be minimized. |
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ISSN: | 0958-0670 0144-8757 1469-445X |
DOI: | 10.1113/expphysiol.1988.sp003225 |