Edman K A, Elzinga G, Noble M I
Adv Exp Med Biol. 1984;170:739-51. doi: 10.1007/978-1-4684-4703-3_71.
Single frog skeletal muscle fibres were stretched during fused tetanic contractions. The force increase during stretch exhibited a breakpoint at a mean critical length change of 16.6 nm per half sarcomere that was independent of stretch velocity and sarcomere length. The early decaying extra force after stretch (component 2) was removed by a small quick release, leaving a longer lasting component (component 3). The amplitude of release required increased with time up to the angle in the force record during stretch, was constant for the remainder of the stretch and decreased with time after the end of stretch; it was consistently less than the critical amplitude of stretch (above). Component 3 occurred at sarcomere lengths above 2.3 microns and was amplitude dependent. The final force after stretch was usually higher than the isometric force at the starting length of the stretch. Non-uniformity as a cause of this component was examined by (a) laser diffraction studies which showed sarcomere stretch at all locations and (b) 0.6-0.7 mm long segments along the entire fibre which all elongated during stretch. After stretch the sarcomeres and segments were significantly more stable than during control isometric tetani. Segments which were clamped by a servo system demonstrated component 3. Shortening during contraction followed by stretch back to the starting length led to nearly as much force enhancement as stretch alone, suggesting that component 3 is not due to a passive elastic element recruited during activation. An increase in temperature decreased components 1 (velocity dependent force during stretch) and 2 but increased component 3. The critical length features of component 2 suggest a cross-bridge mechanism. However, the sarcomere length dependence of all components differs from that of isometric force and from predictions based on filament overlap.
在强直收缩期间对单个青蛙骨骼肌纤维进行拉伸。拉伸过程中的力增加在每半个肌节平均临界长度变化为16.6纳米时出现一个断点,该断点与拉伸速度和肌节长度无关。拉伸后早期衰减的额外力(成分2)可通过一个小的快速释放消除,留下一个持续时间更长的成分(成分3)。释放所需的幅度随时间增加,直至达到拉伸期间力记录中的角度,在拉伸的其余部分保持恒定,并在拉伸结束后随时间减小;它始终小于拉伸的临界幅度(见上文)。成分3出现在肌节长度超过2.3微米时,且与幅度有关。拉伸后的最终力通常高于拉伸起始长度时的等长力。通过以下方式研究了不均匀性作为该成分原因的情况:(a)激光衍射研究表明所有位置的肌节都有拉伸,以及(b)沿着整个纤维的0.6 - 0.7毫米长的片段在拉伸期间都伸长。拉伸后,肌节和片段比对照等长强直收缩期间明显更稳定。由伺服系统夹紧的片段显示出成分3。收缩期间缩短然后拉伸回到起始长度导致的力增强几乎与单独拉伸一样多,这表明成分3不是由于激活期间募集的被动弹性元件引起的。温度升高会降低成分1(拉伸期间与速度相关的力)和2,但会增加成分3。成分2的临界长度特征表明存在一种横桥机制。然而,所有成分的肌节长度依赖性与等长力以及基于细丝重叠的预测不同。