Key result
Sinusoidal length changes applied to activated muscle fibers induced cross-bridge dependent thixotropy at frequencies above 1 Hz and cross-bridge independent rheopexy at frequencies below 1 Hz.
Muscle fiber thixotropy at >1 Hz is cross-bridge dependent, whereas rheopexy at <1 Hz involves a non-cross-bridge mechanism.
Length changes of muscle fibers have previously been shown to result in a temporary reduction in fiber stiffness that is referred to as thixotropy. Understanding the mechanism of this thixotropy is important to our understanding of muscle function since there are many instances in which muscle is subjected to repeated patterns of lengthening and shortening. By applying sinusoidal length changes to one end of single permeabilized muscle fibers and measuring the force response at the opposite end, we studied the history-dependent stiffness of both relaxed and activated muscle fibers. For length change oscillations greater than 1 Hz, we observed thixotropic behavior of activated fibers. Treatment of these fibers with EDTA and blebbistatin, which inhibits myosin-actin interactions, quashed this effect, suggesting that the mechanism of muscle fiber thixotropy is cross-bridge dependent. We modeled a half-sarcomere experiencing sinusoidal length changes, and our simulations suggest that thixotropy could arise from force-dependent cross-bridge kinetics. Surprisingly, we also observed that, for length change oscillations less than 1 Hz, the muscle fiber exhibited rheopexy. In other words, the stiffness of the fiber increased in response to the length changes. Blebbistatin and EDTA did not disrupt the rheopectic behavior, suggesting that a non-cross-bridge mechanism contributes to this phenomenon.
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Altman et al. (2015) studied None (In vitro muscle fiber study). Sinusoidal length oscillations vs. Different frequencies and activation states was evaluated on History-dependent stiffness (thixotropy and rheopexy). Sinusoidal length changes applied to activated muscle fibers induced cross-bridge dependent thixotropy at frequencies above 1 Hz and cross-bridge independent rheopexy at frequencies below 1 Hz.
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