Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6085, USA.
J Physiol. 2012 Feb 1;590(3):575-94. doi: 10.1113/jphysiol.2011.220780. Epub 2011 Nov 28.
Bundles of intact fibres from soleus muscles of adult mice were isolated by dissection and one fibre within a bundle was micro-injected with either furaptra or mag-fluo-4, two low-affinity rapidly responding Ca(2+) indicators. Fibres were activated by action potentials to elicit changes in indicator fluorescence (ΔF), a monitor of the myoplasmic free Ca(2+) transient ([Ca(2+)]), and changes in fibre tension. All injected fibres appeared to be slow-twitch (type I) fibres as inferred from the time course of their tension responses. The full-duration at half-maximum (FDHM) of ΔF was found to be essentially identical with the two indicators; the mean value was 8.4 ± 0.3 ms (±SEM) at 16°C and 5.1 ± 0.3 ms at 22°C. The value at 22°C is about one-third that reported previously in enzyme-dissociated slow-twitch fibres that had been AM-loaded with mag-fluo-4: 12.4 ± 0.8 ms and 17.2 ± 1.7 ms. We attribute the larger FDHM in enzyme-dissociated fibres either to an alteration of fibre properties due to the enzyme treatment or to some error in the measurement of ΔF associated with AM loading. ΔF in intact fibres was simulated with a multi-compartment reaction-diffusion model that permitted estimation of the amount and time course of Ca(2+) release from the sarcoplasmic reticulum (SR), the binding and diffusion of Ca(2+) in the myoplasm, the re-uptake of Ca(2+) by the SR Ca(2+) pump, and Δ[Ca(2+)] itself. In response to one action potential at 16°C, the following estimates were obtained: 107 μm for the amount of Ca(2+) release; 1.7 ms for the FDHM of the release flux; 7.6 μm and 4.9 ms for the peak and FDHM of spatially averaged Δ[Ca(2+)]. With five action potentials at 67 Hz, the estimated amount of Ca(2+) release is 186 μm. Two important unknown model parameters are the on- and off-rate constants of the reaction between Ca(2+) and the regulatory sites on troponin; values of 0.4 × 10(8) m(-1) s(-1) and 26 s(-1), respectively, were found to be consistent with the ΔF measurements.
从成年老鼠的比目鱼肌中分离出完整的纤维束,通过在一个纤维束内进行微注射,将两种低亲和力快速反应的 Ca(2+)指示剂 furaptra 或 mag-fluo-4 导入其中。通过动作电位激活纤维,以引起指示剂荧光(ΔF)的变化,这是细胞质游离 Ca(2+)瞬变([Ca(2+)]的监测器)和纤维张力的变化。所有注入的纤维似乎都是慢收缩(I 型)纤维,这是根据它们张力反应的时间过程推断出来的。在 16°C 时,两种指示剂的 ΔF 的半最大值全时程(FDHM)基本相同;平均值为 8.4 ± 0.3 ms(±SEM),在 22°C 时为 5.1 ± 0.3 ms。在 22°C 时,这一数值约为以前在酶解分离的慢收缩纤维中用 mag-fluo-4 加载 AM 后报道的数值的三分之一:12.4 ± 0.8 ms 和 17.2 ± 1.7 ms。我们将酶解分离纤维中较大的 FDHM 归因于酶处理导致的纤维性质的改变,或者与 AM 加载相关的 ΔF 测量中的某些误差。完整纤维中的 ΔF 通过多隔室反应扩散模型进行模拟,该模型允许估计肌浆网(SR)中 Ca(2+)释放的量和时间过程、Ca(2+)在肌浆中的结合和扩散、SR Ca(2+)泵对 Ca(2+)的再摄取以及 Δ[Ca(2+)]本身。在 16°C 时,对一个动作电位的反应得到以下估计值:107 μm 为 Ca(2+)释放量;1.7 ms 为释放通量的 FDHM;7.6 μm 和 4.9 ms 为空间平均 Δ[Ca(2+)]的峰值和 FDHM。在 67 Hz 时,五个动作电位,估计的 Ca(2+)释放量为 186 μm。两个重要的未知模型参数是 Ca(2+)与肌钙蛋白上调节位点之间反应的结合和离解速率常数;分别为 0.4 × 10(8) m(-1) s(-1) 和 26 s(-1),这两个值与 ΔF 的测量结果一致。