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骨骼肌张力上升过程中的横桥运动与僵硬度——一项理论分析。

Cross-bridge movement and stiffness during the rise of tension in skeletal muscle--a theoretical analysis.

作者信息

Månsson A

机构信息

Department of Pharmacology, University of Lund, Sweden.

出版信息

J Muscle Res Cell Motil. 2000 May;21(4):383-403. doi: 10.1023/a:1005682712789.

Abstract

Predictions for the time courses of cross-bridge attachment. N(t), stiffness, S(t), and force, T(t), during the tetanus rise were analysed for a special class of cross-bridge models where cross-bridges initially attach in a non-stereospecific weak-binding state, AW. This state is in rapid equilibrium (equilibrium constant K) with detached states and the force generating transition (rate constant F+) is delayed. One model (model IA) which assumed step-function rise of activation at onset of tetanus, gave a poor fit to the experimental data (judged by root mean square error, RMSe approximately 0.038) but the experimentally observed lead of N(t) over T(t) was reproduced qualitatively. An activation mechanism where K increased towards its maximum value according to an exponential function (Model IB) improved the fit considerably (RMSe approximately 0.013). However, the activation time constant (r = 30 ms) derived in the fit was too high to reflect Ca2+ binding to troponin. In a further developed model (model II) both Ca2+ -binding to troponin and cross-bridge attachment were assumed to be required for full activation. This more complex model gave a good fit to the experimental data (RMSe approximately 0.013) with a realistic time constant for Ca2+ binding to troponin (9 ms). In both model IB and model II the best fit was obtained with F+ approximately 40 s(-1). An extended version of model IB, with distributed cross-bridge attachment and a series elastic element, gave a fit of similar quality (RMSe approximately 0.009) as obtained with model IB and model II and with a similar value of F+. The results support the view that weakly bound cross-bridges (state AW) may account for the lead of cross-bridge movement over force during tension rise. It is also shown that, if the stiffness of the myofilaments is non-linear (stiffness increasing with tension) the experimentally observed lead of S(t) over T(t) may, to a significant degree, be attributed to cross-bridges in the state AW.

摘要

对横桥附着时间进程的预测。分析了在破伤风上升过程中横桥模型特定类别下的横桥附着数量N(t)、刚度S(t)和力T(t),这类模型中横桥最初以非立体特异性弱结合状态AW附着。该状态与解离状态处于快速平衡(平衡常数K),且产生力的转变(速率常数F+)延迟。一个模型(模型IA)假设在破伤风开始时激活呈阶跃函数上升,与实验数据拟合不佳(通过均方根误差判断,RMSe约为0.038),但定性地再现了实验观察到的N(t)领先于T(t)的现象。一种激活机制,即K根据指数函数向其最大值增加(模型IB),显著改善了拟合效果(RMSe约为0.013)。然而,拟合得出的激活时间常数(τ = 30 ms)过高,无法反映Ca2+与肌钙蛋白的结合。在进一步发展的模型(模型II)中,假设完全激活需要Ca2+与肌钙蛋白结合以及横桥附着。这个更复杂的模型与实验数据拟合良好(RMSe约为0.013),且Ca2+与肌钙蛋白结合的时间常数符合实际(9 ms)。在模型IB和模型II中,当F+约为40 s-1时都获得了最佳拟合。模型IB的扩展版本,具有分布式横桥附着和串联弹性元件,给出了与模型IB和模型II相似质量的拟合(RMSe约为0.009),且F+值相似。结果支持这样的观点,即弱结合横桥(状态AW)可能解释了张力上升过程中横桥运动领先于力的现象。还表明,如果肌丝的刚度是非线性的(刚度随张力增加),实验观察到的S(t)领先于T(t)在很大程度上可能归因于处于状态AW的横桥。

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