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首页> 外文期刊>Journal of Muscle Research and Cell Motility >Effects of membrane depolarization and changes in extracellular (K(+)) on the Ca (2+) transients of fast skeletal muscle fibers. Implications for muscle fatigue.
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Effects of membrane depolarization and changes in extracellular (K(+)) on the Ca (2+) transients of fast skeletal muscle fibers. Implications for muscle fatigue.

机译:膜去极化和细胞外(K(+))的变化对快速骨骼肌纤维的Ca(2+)瞬变的影响。对肌肉疲劳的影响。

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Repetitive activation of skeletal muscle fibers leads to a reduced transmembrane K(+) gradient. The resulting membrane depolarization has been proposed to play a major role in the onset of muscle fatigue. Nevertheless, raising the extracellular K(+) K(+)(O) concentration ([K(+)](O)) to 10 mM potentiates twitch force of rested amphibian and mammalian fibers. We used a double Vaseline gap method to simultaneously record action potentials (AP) and Ca(2+) transients from rested frog fibers activated by single and tetanic stimulation (10 pulses, 100 Hz) at various [K(+)](O) and membrane potentials. Depolarization resulting from current injection or raised [Formula: see text] produced an increase in the resting [Ca(2+)]. Ca(2+) transients elicited by single stimulation were potentiated by depolarization from -80 to -60 mV but markedly depressed by further depolarization. Potentiation was inversely correlated with a reduction in the amplitude, overshoot and duration of APs. Similar effects were found for the Ca(2+) transients elicited by the first pulse of 100 Hz trains. Depression or block of Ca(2+) transient in response to the 2nd to 10th pulses of 100 Hz trains was observed at smaller depolarizations as compared to that seen when using single stimulation. Changes in Ca(2+) transients along the trains were associated with impaired or abortive APs. Raising [K(+)](O) to 10 mM potentiated Ca(2+) transients elicited by single and tetanic stimulation, while raising [K(+)](O) to 15 mM markedly depressed both responses. The effects of 10 mM K(+)(O) on Ca(2+) transients, but not those of 15 mM K(+)(O), could be fully reversed by hyperpolarization. The results suggests that the force potentiating effects of 10 mM K(+)(O) might be mediated by depolarization dependent changes in resting [Ca(2+)] and Ca(2+) release, and that additional mechanisms might be involved in the effects of 15 mM K(+)(O) on force generation.
机译:骨骼肌纤维的重复激活导致跨膜K(+)梯度降低。已经提出,所得的膜去极化在肌肉疲劳的发作中起主要作用。但是,将细胞外K(+)K(+)(O)浓度([K(+)](O))提高到10 mM可以增强静止的两栖动物和哺乳动物纤维的抽搐力。我们使用双Vaseline间隙方法同时记录了在各种[K(+)](O)下通过单次和强直刺激(10个脉冲,100 Hz)激活的静止青蛙纤维中的动作电位(AP)和Ca(2+)瞬态。和膜电位。由电流注入引起的去极化或升高的[公式:参见文本]导致静息[Ca(2+)]的增加。 Ca(2+)瞬变由单次刺激引起的从-80到-60 mV的去极化作用得到增强,但是通过进一步的去极化作用却明显地被抑制了。增强作用与AP的幅度,过冲和持续时间的减少呈负相关。对于由100 Hz列车的第一个脉冲引起的Ca(2+)瞬变,发现了类似的影响。与使用单次刺激时相比,在较小的去极化下观察到了响应于100 Hz列车的第2至第10脉冲的Ca(2+)瞬变的抑制或阻滞。沿列车的Ca(2+)瞬变变化与AP受损或流产有关。将[K(+)](O)升高到10 mM增强的Ca(2+)瞬变,由单个和强直刺激引起,而将[K(+)](O)升高到15 mM则显着抑制了这两种响应。 10 mM K(+)(O)对Ca(2+)瞬态的影响,而不是15 mM K(+)(O)的影响,可以通过超极化完全逆转。结果表明10 mM K(+)(O)的力量增强作用可能是由静息[Ca(2+)]和Ca(2+)释放中依赖于去极化的变化所介导的,并且可能涉及其他机制15 mM K(+)(O)对力产生的影响。

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