Miledi R, Parker I, Zhu P H
J Physiol. 1983 Nov;344:233-41. doi: 10.1113/jphysiol.1983.sp014936.
Strength-duration curves were measured for voltage-clamp depolarizations required to elicit a just detectable rise in intracellular calcium, as monitored using arsenazo III, in frog twitch muscle fibres. In normal Ringer solution, the threshold for a 5 sec duration depolarization was about 5 mV more negative than for a 200 msec duration pulse. The shift in threshold comparing 200 msec and 5 sec pulses was almost abolished in bathing solutions including magnesium or nickel (4 mM), or where the free calcium concentration was buffered. The shift in threshold was little changed by substitution of barium for calcium. These results can be explained by supposing that the 5 sec depolarization activates an inward calcium flux across the T-tubule membrane, which decreases the calcium concentration in the tubules, and hence alters the threshold for activation of excitation-contraction (e.-c.) coupling because of surface charge effects.
在青蛙单收缩肌纤维中,测量引发细胞内钙可检测到的升高所需的电压钳去极化的强度-持续时间曲线,细胞内钙升高通过偶氮胂III进行监测。在正常任氏溶液中,5秒持续时间去极化的阈值比200毫秒持续时间脉冲的阈值负约5毫伏。在含有镁或镍(4毫摩尔)的浴液中,或在游离钙浓度被缓冲的情况下,比较200毫秒和5秒脉冲时阈值的变化几乎消失。用钡替代钙时,阈值变化不大。这些结果可以通过假设5秒去极化激活了跨T小管膜的内向钙通量来解释,这会降低小管中的钙浓度,从而由于表面电荷效应改变兴奋-收缩(e.-c.)偶联的激活阈值。