Key result
Continuous stimulation of rabbit skeletal muscle at 2.5 Hz for 12 weeks induced a fast-oxidative phenotype with high fatigue resistance but minimal slow myosin isoform synthesis compared to 10 Hz.
Continuous stimulation at 2.5 Hz transforms fast skeletal muscles to a fast-oxidative phenotype with high fatigue resistance without complete conversion to slow myosin isoforms.
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Hypothesis-generating for frequency-specific muscle adaptation; leaves open translation to human or cardiac applications.
We studied changes in the mechanical properties and myosin isoform composition of rabbit tibialis anterior muscles that were subjected to continuous stimulation at 2.5 Hz for up to 12 wk. The effects of stimulation at 2.5 Hz were less profound than those observed for the same duration of stimulation at 10 Hz (12). Stimulation at 10 Hz for 12 wk induced complete transformation to a slow-contracting muscle homogeneous in slow myosin isoforms; stimulation for the same period at 2.5 Hz resulted in moderate changes in contractile speed and a very small increase in the synthesis of slow myosin isoforms. On the other hand, the fatigue resistance of muscles stimulated at 2.5 Hz was as great, in both isometric and dynamic fatigue tests, as that of the muscles stimulated at 10 Hz. Thus entire fast skeletal muscles can be transformed to a state in which fast myosin isoforms continue to be synthesized, but the oxidative capacity is sufficient to support sustained working at a higher power output than that associated with slow muscle.
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Jarvis et al. (1996) studied this question. Continuous muscle stimulation at 2.5 Hz vs. Continuous muscle stimulation at 10 Hz was evaluated on Changes in mechanical properties, myosin isoform composition, and fatigue resistance. Continuous stimulation of rabbit skeletal muscle at 2.5 Hz for 12 weeks induced a fast-oxidative phenotype with high fatigue resistance but minimal slow myosin isoform synthesis compared to 10 Hz.
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