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一种力产生模型,该模型解释了横纹肌纤维电刺激后横桥附着与力之间的延迟。

A model of force production that explains the lag between crossbridge attachment and force after electrical stimulation of striated muscle fibers.

作者信息

Bagni M A, Cecchi G, Schoenberg M

机构信息

Dipartimento di Scienze Fisiologiche, Universita degli Studi, Firenze, Italy.

出版信息

Biophys J. 1988 Dec;54(6):1105-14. doi: 10.1016/S0006-3495(88)83046-7.

Abstract

Whereas the mechanical behavior of fully activated fibers can be explained by assuming that attached force-producing crossbridges exist in at least two configurations, one exerting more force than the other (Huxley A. F., and R. M. Simmons. 1971. Nature [Lond.]. 233:533-538), and the behavior of relaxed fibers can be explained by assuming a single population of weakly binding rapid-equilibrium crossbridges (Schoenberg, M. 1988. Biophys. J. 54:135-148), it has not been possible to explain the transition between rest and activation in these terms. The difficulty in explaining why, after electrical stimulation of resting intact frog skeletal muscle fibers at 1-5 degrees C, force development lags stiffness development by more than 15 ms has led a number of investigators to postulate additional crossbridge states. However, postulation of an additional crossbridge state will not explain the following three observations: (a) Although the lag between force and stiffness is very different after stimulation, during the redevelopment of force after an extended period of high velocity shortening, and during relaxation of a tetanus, nonetheless, the plots of force versus stiffness in each of these cases are approximately the same. (b) When the lag between stiffness and force during the rising phase of a twitch is changed nearly fourfold by changing temperature, again the plot of force versus stiffness remains essentially unchanged. (c) When a muscle fiber is subjected to a small quick length change, the rate constant for the isometric force recovery is faster when the length change is applied during the rising phase of a tenanus than when it is applied on the plateau. We have been able to explain all the above findings using a model for force production that is similar to the 1971 model of Huxley and Simmons, but which makes the additional assumption that the force-producing transition envisioned by them is a cooperative one, with the back rate constant of the force-producing transition decreasing as more crossbridges attach.

摘要

虽然完全激活的纤维的力学行为可以通过假设附着的产生力的横桥至少存在两种构型来解释,其中一种构型产生的力比另一种大(赫胥黎A.F.和R.M.西蒙斯,1971年,《自然》[伦敦],233:533 - 538),而松弛纤维的行为可以通过假设存在单一群体的弱结合快速平衡横桥来解释(舍恩伯格,M.,1988年,《生物物理杂志》,54:135 - 148),但用这些术语还无法解释静息和激活之间的转变。在1 - 5摄氏度下对完整的静息青蛙骨骼肌纤维进行电刺激后,力的发展滞后于刚度的发展超过15毫秒,解释这一现象的困难导致许多研究者假设存在额外的横桥状态。然而,假设存在额外的横桥状态并不能解释以下三个观察结果:(a)尽管刺激后、长时间高速缩短后力的重新发展过程中以及强直收缩的松弛过程中,力和刚度之间的滞后差异很大,但在这些情况下,力与刚度的关系图大致相同。(b)当通过改变温度使单收缩上升阶段刚度和力之间的滞后变化近四倍时,力与刚度的关系图再次基本保持不变。(c)当肌肉纤维受到小的快速长度变化时,在强直收缩上升阶段施加长度变化时等长力恢复的速率常数比在平台期施加时更快。我们能够使用一个力产生模型来解释上述所有发现,该模型类似于1971年赫胥黎和西蒙斯的模型,但额外假设他们所设想的产生力的转变是协同的,随着更多横桥附着,产生力的转变的逆向速率常数会降低。

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