Stehle R, Solzin J, Iorga B, Gomez D, Blaudeck N, Pfitzer G
Institute of Vegetative Physiology, and Center of Molecular Medicine Cologne, University of Cologne, Robert-Koch-Str. 39, D-50931, Köln, Germany.
J Muscle Res Cell Motil. 2006;27(5-7):423-34. doi: 10.1007/s10974-006-9072-7. Epub 2006 Aug 9.
Sudden Ca2+ removal from isometrically contracting cardiac myofibrils induces a biphasic relaxation: first a slow, linear force decline during which sarcomeres remain isometric and then a rapid, exponential decay originating from sequential lengthening, i.e., successive mechanical relaxation, of individual sarcomeres (Stehle et al. 2002; Biophys J 83:2152-2162). Step-stretches were applied to the myofibrils, in order to study the mechanical properties of sarcomeres during this dynamic relaxation process. Stretch applied soon (approximately 10 ms) after Ca2+ removal accelerated the initiation of the rapid, exponential force decay and of the sequential sarcomere lengthening. After the stretch, a short, transient period (approximately 24 ms) remained, during which time force was enhanced and sarcomeres were homogenously elongated by the stretch. This period was similar to the duration of the switching-off of troponin C in myofibrils, as measured by stopped-flow. In contrast, when the stretch was applied during the rapid, exponential relaxation phase, force quickly decayed after stretch, back to the force level of isometric controls or even lower. Smaller stretches lengthened only those sarcomeres that were located at the wave front of the sequential sarcomere relaxation. The more the stretch-size was increased, the more of the contracting sarcomeres became lengthened by the stretch; those sarcomeres that were relaxed prior to stretch were barely elongated. These results indicate that the stretch accelerates myofibrillar relaxation by forcing the cross-bridges in contracting sarcomeres to detach. Subsequent rapid cross-bridge reattachment occurs during a short period after Ca2+ removal until troponin C is switched off. However, this switch off occurs approximately 5 times too fast to directly rate-limit the force relaxation under the isometric condition. After troponin C is switched off, stretching induces cross-bridge detachment without subsequent reattachment, and force rapidly decays below the isometric level. This may explain the rapid distention of the ventricular myocardium during early diastolic filling.
从等长收缩的心肌肌原纤维中突然去除Ca2+会引发双相松弛:首先是缓慢的线性力下降,在此期间肌节保持等长,然后是快速的指数衰减,这源于单个肌节的顺序延长,即连续的机械松弛(施特勒等人,2002年;《生物物理杂志》83:2152 - 2162)。对肌原纤维施加阶跃拉伸,以研究在此动态松弛过程中肌节的力学特性。在去除Ca2+后不久(约10毫秒)施加拉伸会加速快速指数力衰减和肌节顺序延长的起始。拉伸后,会有一个短暂的瞬态期(约24毫秒),在此期间力增强,肌节因拉伸而均匀伸长。这个时期与通过停流测量的肌原纤维中肌钙蛋白C关闭的持续时间相似。相反,当在快速指数松弛阶段施加拉伸时,拉伸后力会迅速衰减,回到等长对照的力水平甚至更低。较小的拉伸仅延长那些位于顺序肌节松弛波前的肌节。拉伸大小增加越多,收缩的肌节被拉伸延长的就越多;那些在拉伸前已松弛的肌节几乎不被拉长。这些结果表明,拉伸通过迫使收缩肌节中的横桥分离来加速肌原纤维松弛。在去除Ca2+后短时间内会发生随后的快速横桥重新附着,直到肌钙蛋白C关闭。然而,这种关闭发生得太快,大约快5倍,无法直接在等长条件下限制力的松弛速率。肌钙蛋白C关闭后,拉伸诱导横桥分离且无随后的重新附着,力迅速衰减至等长水平以下。这可能解释了舒张早期充盈期间心室心肌的快速扩张。