Human Performance Laboratory, Faculty of Kinesiology, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Department of Physiology and Pharmacology, Karolinska Institutet, SE-171 77, Stockholm, Sweden.
Pflugers Arch. 2018 Aug;470(8):1243-1254. doi: 10.1007/s00424-018-2143-y. Epub 2018 Apr 18.
Fatigue of single mouse fibers during repeated high-frequency stimulation results initially from decreased Ca sensitivity while free myoplasmic calcium concentration ([Ca]) increases, followed by decreasing [Ca]. Recovery of active force with low-frequency stimulation is slow and persistent fatigue results from low [Ca]. However, the consequences of intermittent submaximal contractions are not known. The aim of the present study was to investigate the changes in [Ca] and active force during intermittent submaximal contractions and subsequent recovery. Single fibers of mouse flexor digitorum brevis muscles at 32 °C were stimulated with 40 or 50 Hz, for 350 ms every 2 s for 2 min and then every 1 s until < 40% of initial force. Values obtained during the intermittent stimulation were compared with a control force-[Ca] relationship. A "P"-shaped pattern in the force-[Ca] relationship was observed during intermittent stimulation. Early in the intermittent stimulation, [Ca] increased while active force decreased. Subsequent force potentiation was accompanied by increased Ca sensitivity. Later, as active force declined, [Ca] decreased significantly (p < 0.001). This was followed, in the final phase, by a significant decrease in Ca sensitivity determined by [Ca] at half-maximal force (Ca) (p = 0.001). Low-frequency fatigue persisted during recovery while Ca was not significantly different from prefatigue (p > 0.5). In conclusion, the main mechanism of fatigue is due to decreases in both [Ca] and Ca sensitivity following the initial force potentiation. The intermittent submaximal contractions resulted in persistent low-frequency fatigue seen during recovery, which was explained by depressed [Ca] with no change in Ca sensitivity.
在重复的高频刺激下,单个鼠纤维的疲劳最初是由于 Ca 敏感性降低,而游离肌浆钙浓度 ([Ca]) 增加,随后 [Ca] 降低。低频刺激下主动力的恢复缓慢,持续的疲劳是由于 [Ca] 低。然而,间歇性亚最大收缩的后果尚不清楚。本研究的目的是研究间歇性亚最大收缩过程中及随后恢复期间 [Ca] 和主动力的变化。在 32°C 下,使用 40 或 50Hz 的频率刺激小鼠趾短屈肌的单个纤维,每 2 秒刺激 350ms,持续 2 分钟,然后每 1 秒刺激一次,直到初始力 < 40%。将获得的值与对照力-[Ca] 关系进行比较。在间歇性刺激过程中观察到力-[Ca] 关系呈“P”形。在间歇性刺激的早期,[Ca] 增加,而主动力下降。随后的力增强伴随着 Ca 敏感性增加。随后,随着主动力下降,[Ca] 显著下降(p<0.001)。随后,在最后阶段,半最大力时的 [Ca](Ca)决定的 Ca 敏感性显著降低(p=0.001)。在恢复期间持续存在低频疲劳,而 Ca 与疲劳前无显著差异(p>0.5)。总之,疲劳的主要机制是在初始力增强后 [Ca] 和 Ca 敏感性降低。间歇性亚最大收缩导致恢复期间持续的低频疲劳,这可以用 [Ca] 降低而 Ca 敏感性没有变化来解释。