Paul R J, Strauss J D, Krisanda J M
Department of Physiology and Biophysics, College of Medicine, University of Cincinnati, OH 45267-0576.
Prog Clin Biol Res. 1987;245:319-32.
In smooth muscle isometric force, shortening velocity, the ATP utilization under isometric conditions, and tension cost are all functions of calcium. This suggests that both cross bridge number and cycle rate are dependent on calcium. On the other hand, the series elastic component does not exhibit a significant dependence on calcium under conditions in which Vus can be increased with little change in Fo. And although the data is not as extensive, the efficiency in working producing contractions is not a strong function of calcium. Our challenge is to fit these mechanical and energetic data into a mechanism which fits the ever growing and controversial body of evidence on the biochemical basis for the action of calcium on the contractile apparatus. At present the most striking feature is the observation that calcium can control the velocity in a manner which is independent of isometric force and efficiency. This would appear to favor a mechanism in which calcium directly affected cross bridge cycle rate in the absence of an internal load.
在平滑肌等长力、缩短速度、等长条件下的ATP利用以及张力消耗方面,钙都起着作用。这表明横桥数量和循环速率都依赖于钙。另一方面,在Vus能够增加而Fo变化很小的条件下,串联弹性成分对钙没有显著依赖性。而且尽管数据不够广泛,但产生收缩的工作效率并非钙的强函数。我们面临的挑战是将这些力学和能量学数据纳入一个机制,该机制要符合关于钙对收缩装置作用的生化基础的不断增长且存在争议的证据体系。目前最显著的特征是观察到钙能够以一种独立于等长力和效率的方式控制速度。这似乎支持一种机制,即钙在没有内部负荷的情况下直接影响横桥循环速率。