Pape P C, Jong D S, Chandler W K
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510-8026, USA.
J Gen Physiol. 1996 Jan;107(1):79-101. doi: 10.1085/jgp.107.1.79.
Cut muscle fibers from Rana temporaria were mounted in a double Vaseline-gap chamber and equilibrated with an end-pool solution that contained 20 mM EGTA and 1.76 mM Ca (sarcomere length, 3.3-3.8 microns; temperature, 14-16 degrees C). Sarcoplasmic reticulum (SR) Ca release, delta[CaT], was estimated from changes in myoplasmic pH (Pape, P.C., D.-S. Jong, and W.K. Chandler. 1995. J. Gen. Physiol. 106:259-336). The maximal value of delta[CaT] obtained during a depleting depolarization was assumed to equal the SR Ca content before stimulation, [CaSR]R (expressed as myoplasmic concentration). After a depolarization to -55 to -40 mV in fibers with [CaSR]R = 1,000-3,000 microM, currents from intramembranous charge movement, Icm, showed an early I beta component. This was followed by an I gamma hump, which decayed within 50 ms to a small current that was maintained for as long as 500 ms. This slow current was probably a component of Icm because the amount of OFF charge, measured after depolarizations of different durations, increased according to the amount of ON charge. Icm was also measured after the SR had been depleted of most of its Ca, either by a depleting conditioning depolarization or by Ca removal from the end pools followed by a series of depleting depolarizations. The early I beta component was essentially unchanged by Ca depletion, the I gamma hump was increased (for [CaSR]R > 200 microM), the slow component was eliminated, and the total amount of OFF charge was essentially unchanged. These results suggest that the slow component of ON Icm is not movement of a new species of charge but is probably movement of Q gamma that is slowed by SR Ca release or some associated event such as the accompanying increase in myoplasmic free [Ca] that is expected to occur near the Ca release sites. The peak value of the apparent rate constant associated with this current, 2-4%/ms at pulse potentials between -48 and -40 mV, is decreased by half when [CaSR]R approximately equal to 500-1,000 microM, which gives a peak rate of SR Ca release of approximately 5-10 microM/ms.
从林蛙身上切下的肌肉纤维被安装在一个双凡士林间隙室中,并用一种终池溶液进行平衡,该终池溶液含有20 mM乙二醇双四乙酸(EGTA)和1.76 mM钙(肌节长度为3.3 - 3.8微米;温度为14 - 16摄氏度)。肌浆网(SR)钙释放量,即Δ[CaT],是根据肌浆pH值的变化来估算的(帕普,P.C.,D.-S. 钟,以及W.K. 钱德勒。1995年。《普通生理学杂志》106:259 - 336)。在耗尽性去极化过程中获得的Δ[CaT]的最大值被假定等于刺激前SR的钙含量,即[CaSR]R(以肌浆浓度表示)。在[CaSR]R = 1000 - 3000微摩尔的纤维中,去极化至 - 55至 - 40毫伏后,膜内电荷移动电流Icm显示出一个早期的Iβ成分。随后是一个Iγ峰,它在50毫秒内衰减为一个小电流,并持续长达500毫秒。这个缓慢电流可能是Icm的一个成分,因为在不同持续时间的去极化后测量的关闭电荷量根据开启电荷量而增加。在SR中的大部分钙被耗尽后,也测量了Icm,这要么是通过耗尽性预处理去极化,要么是通过从终池中去除钙,然后进行一系列耗尽性去极化。早期的Iβ成分基本上不受钙耗尽的影响,Iγ峰增加了(对于[CaSR]R > 200微摩尔),缓慢成分被消除,并且关闭电荷的总量基本上不变。这些结果表明,开启Icm的缓慢成分不是一种新的电荷移动,而可能是Qγ的移动,它被SR钙释放或一些相关事件(如预期在钙释放位点附近发生的肌浆游离[Ca]的伴随增加)减慢。与该电流相关的表观速率常数的峰值,在脉冲电位为 - 48至 - 40毫伏之间时为2 - 4%/毫秒,当[CaSR]R约等于500 - 1000微摩尔时减半,这给出了约5 - 10微摩尔/毫秒的SR钙释放峰值速率。