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电压-依赖的激发-收缩偶联失活的作用

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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 (Q1), (2) the charge movement measured in fibres inactivated by depolarization (Q2) and (3) on the steady state VDI of Q1 and Ca2+ release. Our findings were: (1) The central voltage of Q1 was negatively displaced by perchlorate from ?29.0 ± 1.6 to ?38.4 ± 1.7 mV (n = 4). The maximum Q1 was not significantly affected while the slope of the Q1 vs. V was increased by perchlorate. (2) The central voltage of Q2 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 Q1 went from ?39.3 ± 1.8 to ?48.6 ± 1.2 mV (mean ± SEM, n = 6). Perchlorate had a paradoxical effect on Ca2+ 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 μM/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 μM/ms, n = 9). The above findings suggest that the effect on the steady state inactivation is a direct consequence of the negative shift in Q1 activation. The negative shift in the steady state inactivation of Q1 correlated well with the effect on Ca2+ 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对以下方面的影响:(1)激活释放的电荷运动(Q1 ),(2)在通过去极化失活的纤维中测得的电荷运动(Q2 )和(3)释放Q1 和Ca2 + 的稳态VDI。我们的发现是:(1)高氯酸盐使Q1 的中心电压从±29.0±1.6负移至±38.4±1.7 mV(n = 4)。最大的Q1 没有受到显着影响,而高氯酸盐增加了Q1 与V的斜率。 (2)Q2 的中心电压从?91.6±1.4变为?102.3±1.5 mV(n = 4)。 (3)Q1 的稳态灭活曲线的中心电压从?39.3±1.8到?48.6±1.2 mV(平均值±SEM,n = 6)。高氯酸盐对Ca2 +的释放具有反常的影响,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),具有抑制作用。当以去极化的保持电势应用于光纤时(峰值释放通量从3.9±0.9降低至2.0±0.5μM/ ms,n = 9),会产生明显的影响。上述发现表明,对稳态失活的影响是Q1 激活负向移动的直接结果。 Q1 稳态失活的负移与对Ca2 + 释放的影响密切相关。

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