Harris D E, Warshaw D M
Department of Physiology and Biophysics, University of Vermont, College of Medicine, Burlington 05405.
J Gen Physiol. 1990 Sep;96(3):581-601. doi: 10.1085/jgp.96.3.581.
In single smooth muscle cells, shortening velocity slows continuously during the course of an isotonic (fixed force) contraction (Warshaw, D.M. 1987. J. Gen. Physiol. 89:771-789). To distinguish among several possible explanations for this slowing, single smooth muscle cells were isolated from the gastric muscularis of the toad (Bufo marinus) and attached to an ultrasensitive force transducer and a length displacement device. Cells were stimulated electrically and produced maximum stress of 144 mN/mm2. Cell force was then reduced to and maintained at preset fractions of maximum, and cell shortening was allowed to occur. Cell stiffness, a measure of relative numbers of attached crossbridges, was measured during isotonic shortening by imposing 50-Hz sinusoidal force oscillations. Continuous slowing of shortening velocity was observed during isotonic shortening at all force levels. This slowing was not related to the time after the onset of stimulation or due to reduced isometric force generating capacity. Stiffness did not change significantly over the course of an isotonic shortening response, suggesting that the observed slowing was not the result of reduced numbers of cycling crossbridges. Furthermore, isotonic shortening velocity was better described as a function of the extent of shortening than as a function of the time after the onset of the release. Therefore, we propose that slowing during isotonic shortening in single isolated smooth muscle cells is the result of an internal load that opposes shortening and increases as cell length decreases.
在单个平滑肌细胞中,等张(固定力)收缩过程中缩短速度持续减慢(沃肖,D.M. 1987年。《普通生理学杂志》89:771 - 789)。为了区分这种减慢的几种可能解释,从蟾蜍(海蟾蜍)胃肌层分离出单个平滑肌细胞,并将其连接到一个超灵敏力传感器和一个长度位移装置上。用电刺激细胞,产生的最大应力为144 mN/mm²。然后将细胞力降至并维持在最大值的预设比例,并允许细胞发生缩短。在等张缩短过程中,通过施加50赫兹的正弦力振荡来测量细胞刚度,这是附着横桥相对数量的一种度量。在所有力水平下的等张缩短过程中均观察到缩短速度持续减慢。这种减慢与刺激开始后的时间无关,也不是由于等长力产生能力降低所致。在等张缩短反应过程中,刚度没有显著变化,这表明观察到的减慢不是循环横桥数量减少的结果。此外,等张缩短速度更好地描述为缩短程度的函数,而不是释放开始后时间的函数。因此,我们提出,单个分离的平滑肌细胞在等张缩短过程中的减慢是一种内部负荷的结果,该负荷对抗缩短并随着细胞长度的减小而增加。