首页> 美国卫生研究院文献>The Journal of Physiology >Dissociation of force from myofibrillar MgATPase and stiffness at short sarcomere lengths in rat and toad skeletal muscle.
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Dissociation of force from myofibrillar MgATPase and stiffness at short sarcomere lengths in rat and toad skeletal muscle.

机译:大鼠和蟾蜍骨骼肌中肌原纤维MgATPase的力解离和短肌节长度上的僵硬。

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摘要

1. Single fast-twitch fibres from the extensor digitorum longus muscle of the rat, Rattus norvegicus, and single twitch fibres from the iliofibularis muscle of the cane toad, Bufo marinus, were mechanically skinned and then used to measure maximally Ca2+-activated [( Ca2+] greater than 0.03 mmol l-1) isometric force production, myofibrillar MgATPase activity and fibre stiffness at different sarcomere lengths. MgATP hydrolysis was linked by an enzyme cascade to the oxidation of NADH (nicotinamide adenine dinucleotide, reduced form) and was monitored by a microfluorimetric system. Fibre stiffness was measured from the amplitude of force oscillations generated by small sinusoidal length changes. 2. At sarcomere lengths which were optimal for isometric force production (around 2.7 microns for rat and 2.2 microns for toad fibres) the myofibrillar MgATPase activity (mean +/- S.E.M.) at 21-22 degrees C was found to be 3.80 +/- 0.53 molecules MgATP hydrolysed s-1 per myosin head for eight rat fibres and 6.35 +/- 0.77 s-1 per myosin head for four toad fibres. 3. At sarcomere lengths shorter than 2.7 microns in rat fibres and 2.2 microns in toad fibres, MgATPase and stiffness remained elevated and close to their respective values at 2.7 microns in rat fibres and 2.2 microns in toad fibres even when the isometric force decreased to near zero levels. 4. The dissociation at short sarcomere lengths of myofibrillar MgATPase activity and fibre stiffness from isometric force suggests that the cross-bridge cycle is not greatly affected by double actin filament overlap with the myosin filaments at short sarcomere lengths. Moreover, the results suggest that cross-bridges can be formed by myosin with actin filaments projecting from the nearest Z-line and from the Z-line in the other half of the sarcomere. 5. These results help to reconcile energetic and mechanical data obtained by others at short sarcomere lengths and can be explained within the framework of the sliding filament theory.
机译:1.将大鼠伸指长肌(褐家鼠)的单根快肌纤维和甘蔗蟾蜍蟾蜍海马的腓肠肌的单根肌纤维进行机械剥皮,然后用于最大程度地测量Ca2 +活化[ Ca2 +]大于0.03 mmol l-1)的等轴测力产生,肌纤维MgATPase活性和不同肌节长度下的纤维硬度。 MgATP水解通过酶级联反应与NADH(烟酰胺腺嘌呤二核苷酸,还原形式)的氧化联系在一起,并通过微荧光系统进行监测。纤维刚度是由正弦长度变化小的力振荡幅度测量的。 2.在最适合产生等距力的肌节长度(大鼠约2.7微米,蟾蜍纤维约2.2微米)下,发现21-22摄氏度的肌原纤维MgATPase活性(平均值+/- SEM)为3.80 +/-。每条肌球蛋白头0.53分子MgATP水解八种大鼠纤维的s-1,每条肌球蛋白头水解6.35 +/- 0.77 s-1的四种蟾蜍纤维。 3.当大鼠纤维的肌节长度短于2.7微米,蟾蜍纤维的短于2.2微米时,即使等轴测力减小到接近,MgATPase和刚度仍保持升高,并接近于大鼠纤维中的2.7微米和蟾蜍纤维中的2.2微米。零级。 4.肌原纤维MgATPase活性的短肌节长度解离和等轴测力的纤维刚度表明双肌动蛋白丝和肌球蛋白丝在短肌节长度上的重叠对跨桥循环的影响不大。此外,结果表明,肌球蛋白可以形成跨桥,肌动蛋白丝从最近的Z线和肌节另一半的Z线伸出。 5.这些结果有助于协调其他人在短的肌节长度上获得的能量和力学数据,并且可以在滑动丝理论的框架内进行解释。

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