肌酸激酶缺乏小鼠骨骼肌力量和速度的刺激频率依赖性降低。

A De Haan, M Bien, P W Verdijk
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引用次数: 8

摘要

通过对肌酸激酶缺失型和野生型小鼠腓肠肌内侧肌在不同刺激频率下的等距收缩获得力和速度参数。在较高的刺激频率下,肌酸激酶的缺失不影响力的产生。然而,在频率低于140 Hz时,力低于对照组(P < 0.05);在施加的最低频率(80 Hz)下,与野生型肌肉相比,力减少到约60%。相比之下,抽搐力不受影响。当宫缩前有短暂的破伤风(50 ms)时,缺乏肌酸激酶对肌力产生的影响更为明显;在80 Hz刺激下,等距力进一步降低到66.5 +/- 6.2%(平均+/- SD;N =5)缺陷肌肉的单次收缩和约42%的野生型肌肉。抽搐力量现在也减少了(约50%)破伤风后。肌肉的速度在单次收缩中不受影响。然而,在前一次破伤风后,在高频率刺激下,力的上升率降低了约14%。随着频率的降低(低于250赫兹),速度的降低变得更加明显;在80 Hz时,肌酸激酶缺陷肌的发生率仅为55.2 +/- 3.9%(平均+/- SD;N =5)的野生型肌肉。对半松弛时间没有发现缺陷的影响。数据表明,肌酸激酶系统受损导致在次最大刺激频率下激活水平降低,可能是由于重复刺激期间Ca2+释放减少。当磷酸肌酸耗尽时,在正常疲劳肌肉中也可能出现类似的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stimulation frequency-dependent reductions in skeletal muscle force and speed in creatine kinase-deficient mice.

Force and speed parameters were obtained from isometric contractions at different stimulation frequencies of creatine kinase-deficient and wildtype in situ mouse medial gastrocnemius muscles. The absence of creatine kinase did not affect force production at higher stimulation frequencies. However, at frequencies below 140 Hz, forces were lower than the controls (P < 0.05); at the lowest frequency applied (80 Hz) the force was reduced to approximately 60% compared with the wildtype muscles. In contrast, twitch force was not affected. When the contractions were preceded by a brief tetanus (50 ms), the effects of lacking creatine kinase on force production were more pronounced; at 80 Hz stimulation isometric force was further reduced to 66.5 +/- 6.2% (mean +/- SD; n=5) of the single contractions of the deficient muscles and to approximately 42% of the wildtype muscles. Twitch force was now also reduced (by approximately 50%) after the tetanus. The speed of the muscles was not affected in the single contractions. However, after a preceding tetanus, the rate of force rise was reduced by approximately 14% at high frequencies of stimulation. With decreasing frequencies (below 250 Hz), the reduction in speed became more pronounced; at 80 Hz the rate in the creatine kinase-deficient muscles was only 55.2 +/- 3.9% (mean +/- SD; n=5) of the wildtype muscles. No effects of the deficiency were found for the half relaxation times. The data suggest that an impaired creatine kinase system leads to lower activation levels at submaximal stimulation frequencies, possibly by a reduction in Ca2+-release during repetitive stimulation. Similar effects may be expected in normal fatigued muscle when phosphocreatine is depleted.

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