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肌肉振荡的三态模型:正弦分析。

A three-state model for oscillation in muscle: sinusoidal analysis.

作者信息

Murase M, Tanaka H, Nishiyama K, Shimizu H

出版信息

J Muscle Res Cell Motil. 1986 Feb;7(1):2-10. doi: 10.1007/BF01756196.

DOI:10.1007/BF01756196
PMID:3958157
Abstract

The crossbridge mechanism leading to oscillation in insect flight muscle is studied theoretically based on a three-state model proposed by Nishiyama et al. [Biochim. biophys. Acta 460, 523-36 (1977)]. Skeletal muscle as well as insect flight muscle shows. oscillatory contraction. We demonstrate this oscillatory contraction in muscle by choosing proper rate constants among the three states of the model. It is established that our model gives out not only Hill's force-velocity relation but also other mechanical properties of skeletal muscle. The model is then compared with two types of experiment by Kawai & Brandt [J. Musc. Res. Cell Motility 1, 279-303 (1980)] and by Steiger & Rüegg [Pflügers Arch. 307, 1-21 (1969)]. Kawai & Brandt obtained the Nyquist plot showing the relation between the phase shift and the amplitude of tension change in response to sinusoidal length changes at various frequencies. Steiger & Rüegg studied the power output and ATPase activity at various frequencies of the length change. Our theoretical results are in good agreement with the results of these two experiments. To determine the crossbridge mechanism which produces the positive power output, spatio-temporal crossbridge distributions in the three states are calculated. It is shown that, after the stretching phase of sinusoidal change in muscle length, the delayed rise of tension is caused by attachment of crossbridges to the active state via the preactive state while the delayed fall is caused by detachment from the active state after release. To obtain the oscillatory property it is not necessary to assume that stretch in muscle length increases the attaching rate as originally proposed by Thorson & White [Biophys. J. 9, 360-90 (1969)].

摘要

基于西山等人提出的三态模型[《生物化学与生物物理学报》460, 523 - 36 (1977)],对导致昆虫飞行肌肉振荡的横桥机制进行了理论研究。骨骼肌以及昆虫飞行肌肉都表现出振荡收缩。我们通过在模型的三种状态中选择合适的速率常数来证明肌肉中的这种振荡收缩。已确定我们的模型不仅能给出希尔力 - 速度关系,还能给出骨骼肌的其他力学性质。然后将该模型与河合和布兰特[《肌肉研究与细胞运动杂志》1, 279 - 303 (1980)]以及施泰格和吕格[《 Pflügers 文献》307, 1 - 21 (1969)]的两类实验进行比较。河合和布兰特得到了奈奎斯特图,该图显示了在不同频率下,响应正弦长度变化时张力变化的相移与幅度之间的关系。施泰格和吕格研究了在不同长度变化频率下的功率输出和ATP酶活性。我们的理论结果与这两个实验的结果高度吻合。为了确定产生正功率输出的横桥机制,计算了三种状态下的时空横桥分布。结果表明,在肌肉长度正弦变化的拉伸阶段之后,张力的延迟上升是由于横桥通过预激活状态附着到激活状态引起的,而延迟下降是由于释放后从激活状态脱离引起的。为了获得振荡特性,不必像索尔森和怀特最初提出的那样[《生物物理杂志》9, 360 - 90 (1969)]假设肌肉长度的拉伸会增加附着速率。

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