Melzer W, Schneider M F, Simon B J, Szucs G
J Physiol. 1986 Apr;373:481-511. doi: 10.1113/jphysiol.1986.sp016059.
Intramembrane charge movement and myoplasmic free calcium transients (delta[Ca2+]) were monitored in voltage-clamped segments of isolated frog muscle fibres cut at both ends and mounted in a double Vaseline-gap chamber. The fibres were stretched to sarcomere lengths of 3.5-4.6 micron to minimize mechanical movement and the related optical artifacts. The over-all calcium removal capability of each fibre was characterized by analysing the decay of delta[Ca2+] following pulses of several different amplitudes and durations. The rate of sarcoplasmic reticulum (s.r.) calcium release was then calculated for each delta[Ca2+] using the calcium removal properties determined for that fibre. The calculated calcium release wave form reached a relatively early peak and then declined appreciably during a 100-150 ms depolarizing pulse. The voltage dependence of the peak rate of calcium release was steeper and was centred at more positive membrane potentials than the steady-state voltage dependence of charge movement in the same fibres. A considerable fraction of the total intramembrane charge was moved at potentials at which delta[Ca2+] and calcium release were only a few per cent of maximum. This 'subthreshold' charge may correspond to charge moved in preliminary transitions that precede a final charge transition that activates release. A 'stepped on' pulse protocol was used to experimentally separate the subthreshold charge movement from the charge movement of the final transitions that may control calcium release. The stepped on pulse consisted of a set 50 ms pre-pulse to a potential just at or below the potential for detectable delta[Ca2+] followed immediately by a test pulse of varying amplitude and duration. For a wide range of test pulse amplitudes and durations in the stepped on protocol the peak rate of calcium release was linearly related to the charge movement during the test pulse. This result points to a tight control of activation of s.r. calcium release by intramembrane charge movement. The voltage dependence of both charge movement and of the rate of calcium release could be fitted simultaneously with a three-state, two-transition sequential model in which charge moves in both transitions but only the final transition activates s.r. calcium release. A model with three identical and independent charged gating particles per channel gave an equally good fit to the data. Both models closely fit the charge movement and release data except within about 10 mV of the voltage at which release became detectable, where release varied more steeply with membrane potential than predicted by either model.(ABSTRACT TRUNCATED AT 400 WORDS)
在两端切断并安装在双凡士林间隙室中的分离青蛙肌肉纤维的电压钳制节段中,监测膜内电荷移动和肌浆游离钙瞬变(Δ[Ca2+])。将纤维拉伸至肌节长度为3.5 - 4.6微米,以尽量减少机械运动及相关的光学伪影。通过分析几种不同幅度和持续时间的脉冲后Δ[Ca2+]的衰减,来表征每根纤维的总体钙清除能力。然后利用为该纤维确定的钙清除特性,为每个Δ[Ca2+]计算肌浆网(s.r.)钙释放速率。计算得到的钙释放波形在100 - 150毫秒的去极化脉冲期间达到相对较早的峰值,然后明显下降。钙释放峰值速率的电压依赖性比同一纤维中电荷移动的稳态电压依赖性更陡峭,且集中在更正的膜电位。相当一部分总膜内电荷在Δ[Ca2+]和钙释放仅为最大值的百分之几时的电位下移动。这种“阈下”电荷可能对应于在激活释放的最终电荷转变之前的初步转变中移动的电荷。采用“阶跃脉冲”方案从可能控制钙释放的最终转变的电荷移动中实验性地分离出阈下电荷移动。阶跃脉冲由一个50毫秒的预脉冲组成,预脉冲电位刚好处于或低于可检测到Δ[Ca2+]的电位,随后立即是一个幅度和持续时间可变的测试脉冲。在阶跃脉冲方案中,对于广泛的测试脉冲幅度和持续时间,钙释放峰值速率与测试脉冲期间的电荷移动呈线性相关。这一结果表明膜内电荷移动对肌浆网钙释放的激活有严格控制。电荷移动和钙释放速率的电压依赖性可以同时用一个三态、双转变的顺序模型来拟合,其中电荷在两个转变中都移动,但只有最终转变激活肌浆网钙释放。一个每个通道有三个相同且独立的带电门控粒子的模型对数据的拟合同样良好。除了在释放变得可检测的电压约10毫伏范围内,两个模型都能很好地拟合电荷移动和释放数据,在该范围内释放随膜电位的变化比任何一个模型预测的都更陡峭。(摘要截短至400字)