Saldana R P, Smith D A
Department of Physics, Monash University, Clayton, Australia.
J Muscle Res Cell Motil. 1991 Dec;12(6):517-31. doi: 10.1007/BF01738440.
Four aspects of the slow creep of tension and sarcomere lengths observed during fixed-end tetani are studied with computer simulations, using the instantaneous steady-state (adiabatic) approximation. (1) Most aspects of fixed-end creep phenomena can be simulated in the presence of the passive forces which correctly produce initially shortened end sarcomeres. However, the very large maximum tensions observed with fibres of low resting force for sarcomere lengths greater than 3.0 microns cannot be simulated within the adiabatic approximation. (2) Random variations in the passive tension-length curve between different sarcomeres can predict the reported incidence of contracting sarcomeres in the middle of the fibre, while avoiding significant tension creep when a central segment is length-clamped. They can also reverse the velocity of these sarcomeres during creep in fibres with high resting tension, as observed by Altringham and Bottinelli (1985). At sarcomere lengths of greater than or equal to 3.4 microns we find that spatial variations in passive tension strength also contribute to tension creep. (3) Crossbridge fluctuations in active tension have been estimated from the sliding-filament model, and do not contribute significantly to tension creep. (4) The need for inter-sarcomere stiffness or other mechanisms to produce an additional slow rise in tension at long times, and to smooth the sarcomere length distribution, is assessed.
利用瞬时稳态(绝热)近似,通过计算机模拟研究了在固定端强直收缩过程中观察到的张力缓慢变化和肌节长度的四个方面。(1)在存在能正确产生初始缩短的末端肌节的被动力的情况下,可以模拟固定端蠕变现象的大多数方面。然而,在绝热近似范围内,无法模拟在肌节长度大于3.0微米时,低静息力纤维所观察到的非常大的最大张力。(2)不同肌节之间被动力-长度曲线的随机变化可以预测报道的纤维中部收缩肌节的发生率,同时当中央段长度被钳定时避免明显的张力蠕变。它们还可以使高静息张力纤维在蠕变过程中这些肌节的速度反转,正如阿尔tringham和博蒂内利(1985年)所观察到的那样。在肌节长度大于或等于3.4微米时,我们发现被动力强度的空间变化也有助于张力蠕变。(3)根据滑动丝模型估计了主动张力中的横桥波动,其对张力蠕变的贡献不大。(4)评估了肌节间刚度或其他机制在长时间产生额外缓慢张力上升以及使肌节长度分布平滑的必要性。