Tameyasu T
Department of Physiology, St. Marianna University School of Medicine, Kawasaki, Japan.
J Muscle Res Cell Motil. 1992 Dec;13(6):619-29. doi: 10.1007/BF01738251.
The time course of shortening at zero load was studied by the slack test method during tetanic contractions in isolated, single, slow muscle fibres of the crayfish. In 28 of 32 shortenings (from 14 different fibres) a biphasic shortening was seen, which consisted of an initial high-velocity phase lasting 3.3-20.8 ms and a following slow-velocity phase lasting for the entire time examined (up to 89.2 ms). Provided that the shortening occurred uniformly along the fibre length, velocity in the initial phase, V1, of the biphasic shortening was 14.4 +/- 3.4 (mean +/- SD, n = 10) microns s-1 per half sarcomere at Lo, the slack length, at 20 degrees C, while that in the second phase, V2, was 7.4 +/- 1.4 microns s-1 per half sarcomere. Lowering temperature decreased both V1 and V2 with Q10 = 1.4 for V1 and 2.0 for V2. Lowering the external Ca concentration from 15 mM, the standard, to 2 mM resulted in a tetanic tension below one-third of that at 15 mM Ca and decreased both V1 (t test; p < 0.01) and V2 (p < 0.001). Prestretching the fibre to 1.5 Lo had no significant effect on V2 (p < 0.3) but increased V1 (p < 0.001). The distance shortened during the initial high-velocity phase, LV1, was 4.0 +/- 1.8% Lo (mean +/- SD, n = 10) at 20 degrees C or about 0.14 microns per half sarcomere on average. LV1 was independent of the tetanic tension level when it was changed by lowering the external Ca concentration or temperature in the same fibre. Prestretching the fibre to 1.5 Lo, at which the sum of the active and the resting tension was lower than Po at Lo in two of three fibres, increased LV1 significantly (p < 0.001). The independency of LV1 from the tension level indicates that the initial high-velocity phase was not from shortening of some inert components in the fibre. One possibility is that the initial high-velocity phase was brought about by an acceleration of shortening by a compressive force, the origin of which has been discussed. The slow-velocity phase seemed to result from the crossbridge turnover with little exogeneous stress on myofilaments. Four different fibres exhibited an unloaded shortening with a constant velocity during the entire time examined (29.9-61.8 ms). This type of shortening had a velocity between the usual V1 and V2 values, suggesting that a compressive force accelerated the shortening during the entire time.
通过松弛试验法研究了小龙虾离体单根慢肌纤维强直收缩时零负荷下的缩短时程。在32次缩短(来自14条不同纤维)中的28次中,观察到双相缩短,其包括持续3.3 - 20.8毫秒的初始高速相和持续整个观察时间(长达89.2毫秒)的后续低速相。假设沿纤维长度均匀发生缩短,在20℃的松弛长度Lo下,双相缩短初始相的速度V1为每半个肌节14.4±3.4(平均值±标准差,n = 10)微米/秒,而第二相的速度V2为每半个肌节7.4±1.4微米/秒。降低温度会使V1和V2均降低,V1的Q10为1.4,V2的Q10为2.0。将外部钙浓度从标准的15毫摩尔/升降至2毫摩尔/升,导致强直张力低于15毫摩尔/升钙时的三分之一,并使V1(t检验;p < 0.01)和V2(p < 0.001)均降低。将纤维预拉伸至1.5Lo对V2没有显著影响(p < 0.3),但增加了V1(p < 0.001)。在20℃时,初始高速相期间缩短的距离LV1为4.0±1.8%Lo(平均值±标准差,n = 10),或平均每半个肌节约0.14微米。当通过降低同一纤维的外部钙浓度或温度来改变强直张力水平时,LV1与强直张力水平无关。将纤维预拉伸至1.5Lo(在三根纤维中的两根中,此时主动张力和静息张力之和低于Lo时的Po)会显著增加LV1(p < 0.001)。LV1与张力水平无关表明初始高速相并非来自纤维中某些惰性成分的缩短。一种可能性是初始高速相是由压缩力加速缩短导致的,其来源已被讨论。低速相似乎是由于横桥周转且肌丝上几乎没有外源性应力引起的。四条不同的纤维在整个观察时间(29.9 - 61.8毫秒)内表现出匀速的无负荷缩短。这种类型的缩短速度介于通常的V1和V2值之间,表明压缩力在整个时间内加速了缩短。