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首页> 外文期刊>Journal of Muscle Research and Cell Motility >Action of perchlorate on the voltage dependent inactivation of excitation-contraction coupling in frog skeletal muscle fibres.
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Action of perchlorate on the voltage dependent inactivation of excitation-contraction coupling in frog skeletal muscle fibres.

机译:高氯酸盐对青蛙骨骼肌纤维中依赖于激发-收缩偶联的电压失活的作用。

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Perchlorate is an agonist of excitation-contraction coupling (ECC) in skeletal muscle displacing charge movement and release activation towards more negative voltages. Contradictory effects of this compound on the voltage dependent inactivation (VDI) of ECC ranging from no effect to a negative shift have been previously reported. In this study we report the effect of the extracellular application of 8 mM perchlorate to cut frog fibres on: (1) the charge movement that activates release (Q(1)), (2) the charge movement measured in fibres inactivated by depolarization (Q(2)) and (3) on the steady state VDI of Q(1) and Ca(2+) release. Our findings were: (1) The central voltage of Q(1) was negatively displaced by perchlorate from -29.0 +/- 1.6 to -38.4 +/- 1.7 mV (n = 4). The maximum Q(1) was not significantly affected while the slope of the Q(1) vs. V was increased by perchlorate. (2) The central voltage of Q(2) was shifted from -91.6 +/- 1.4 to -102.3 +/- 1.5 mV (n = 4). (3) The central voltage of the steady state inactivation curve of Q(1) went from -39.3 +/- 1.8 to -48.6 +/- 1.2 mV (mean +/- SEM, n = 6). Perchlorate had a paradoxical effect on Ca(2+) release, while potentiated the release flux in fibres held at -90 mV (peak release flux increased from 3.9 +/- 1.1 to 6.8 +/- 1.9 muM/ms, n = 5) it had an inhibitory effect when applied to fibres at a depolarized holding potential (peak release flux decreased from 3.9 +/- 0.9 to 2.0 +/- 0.5 muM/ms, n = 9). The above findings suggest that the effect on the steady state inactivation is a direct consequence of the negative shift in Q(1) activation. The negative shift in the steady state inactivation of Q(1) correlated well with the effect on Ca(2+) release.
机译:高氯酸盐是骨骼肌中兴奋-收缩偶联(ECC)的激动剂,可移动电荷并向更多的负电压释放激活。先前已经报道了该化合物对ECC的电压依赖性失活(VDI)的从无作用到负位移的矛盾作用。在这项研究中,我们报告了细胞外应用8 mM高氯酸盐切割青蛙纤维的作用:(1)激活释放的电荷运动(Q(1)),(2)在通过去极化失活的纤维中测得的电荷运动( Q(1)和Ca(2+)的稳态VDI上的Q(2))和(3)。我们的发现是:(1)高氯酸盐将Q(1)的中心电压从-29.0 +/- 1.6负移至-38.4 +/- 1.7 mV(n = 4)。最大Q(1)不受显着影响,而高氯酸盐使Q(1)与V的斜率增加。 (2)Q(2)的中心电压从-91.6 +/- 1.4变为-102.3 +/- 1.5 mV(n = 4)。 (3)Q(1)的稳态失活曲线的中心电压从-39.3 +/- 1.8变为-48.6 +/- 1.2 mV(平均值+/- SEM,n = 6)。高氯酸盐对Ca(2+)的释放具有矛盾的影响,同时增强了保持在-90 mV的纤维中的释放通量(峰值释放通量从3.9 +/- 1.1增至6.8 +/- 1.9μM/ ms,n = 5)当以去极化的保持电位应用于纤维时,它具有抑制作用(峰值释放通量从3.9 +/- 0.9降低至2.0 +/- 0.5μM/ ms,n = 9)。上述发现表明,对稳态失活的影响是Q(1)激活发生负向移动的直接结果。 Q(1)的稳态失活中的负移与对Ca(2+)释放的影响相关性很好。

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