Aequorin luminescence during contraction of amphibian skeletal muscle.
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Biomedical subjects
Publications and source records attributed to R Rüdel.
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One of the factors evidently responsible for decreasing the force of muscle contraction with shortening is inactivation of the myofibrils in the core of a muscle fiber. Caffeine antagonizes this inactivation and, correspondingly, changes the length-force relationship at short muscle lengths.
The myofibrils in an isolated muscle fiber remain straight during the early part of a lightly loaded contraction initiated by membrane depolarization, but, as shortening continues, myofibrils in the core of the fiber become wavy, which suggests that their activation has been interrupted by shortening of the fiber. This may be a factor determining the length-tension relation at short muscle lengths.
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1. Reversible changes in twitch and tetanus contractions of isolated frog muscle fibres were produced by varying the duration and strength of a transversely applied d.c. stimulus.2. When the stimulus strength was at least 1.1 times threshold the peak force of the contraction elicited was reduced by stimulus durations longer than 1 msec at 20 degrees C, and by durations longer than 3 msec at 2-5 degrees C.3. As the strength of a prolonged stimulus was progressively increased to 3 times rheobase or more, peak twitch and tetanus force declined to 40-70% of the amplitude with short (0.2-0.5 msec) stimuli. The time to peak of the twitch was slightly decreased and the first phase of relaxation was accelerated.4. Cine-micrography of fibres which were permitted to shorten under a light load revealed that the side of the fibre adjacent to the anode was unactivated under conditions which also reduced peak force output.5. With stimulus durations longer than 20 msec, peak force, time to peak, and relaxation time increased as the stimulus strength increased from 2.5 to 3 times rheobase. This might have been produced by a cathodal contracture following the action potential.6. The results are discussed in relation to previous studies of activation in striated muscle.
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