Sipido K R, Maes M, Van de Werf F
Laboratory of Experimental Cardiology, University of Leuven, Belgium.
Circ Res. 1997 Dec;81(6):1034-44. doi: 10.1161/01.res.81.6.1034.
It has been proposed that Ca2+ entry through the Na(+)-Ca2+ exchanger can contribute significantly to the trigger for Ca2+ release from the sarcoplasmic reticulum (SR). We have compared the characteristics of Ca2+ release triggered by reverse-mode Na(+)-Ca2+ exchange and by L-type Ca2+ current (ICaL) during depolarizing steps in single guinea pig ventricular myocytes (whole-cell voltage clamp, fluo 3 and fura-red as [Ca2+]i indicators, 36 +/- 1 degrees C, K(+)-based pipette solution with 20 mmol/L [Na+]). Conditioning pulses to +60 mV ensured comparable Ca2+ loading of the SR. In the presence of ICaL, [Ca2+]i transients typically have an early and rapid rising phase reflecting Ca2+ release, which has a bell-shaped voltage dependence with a peak at +10 mV. With Ca2+ entry through Na(+)-Ca2+ exchange only (20 mumol/L nisoldipine), Ca2+ release flux from the SR is decreased and directly related to the amplitude of the depolarizing step. Ca2+ release is preceded by a significant delay (81 +/- 21 ms at +20 mV, 24 +/- 4 ms at +70 mV) related to Ca2+ entry through the exchanger. Triggered release interrupts Ca2+ entry, as evidenced by reversal of the exchanger current. At potentials positive to +40 mV, Ca2+ influx through Na(+)-Ca2+ exchange, calculated from the outward exchange current, reaches magnitudes comparable to ICaL, but Ca2+ release due to reverse-mode Na(+)-Ca2+ exchange still has a significant delay. We calculated trigger efficiency as the ratio between the maximal rate of Ca2+ release and the Ca2+ influx preceding this release; efficiency of reverse-mode Na(+)-Ca2+ exchange is approximately four times less than that of ICaL. With both ICaL and reverse-mode Na(+)-Ca2+ exchange present, Ca2+ release is triggered by ICaL, and a contribution of reverse-mode Na(+)-Ca2+ exchange to the trigger could not be detected at potentials below +60 mV. These characteristics of reverse-mode Na(+)-Ca2+ exchange predict that its role as a trigger for Ca2+ release during the action potential is likely to be negligible.
有人提出,通过钠钙交换体的钙离子内流可对肌浆网(SR)钙离子释放的触发起重要作用。我们比较了在豚鼠单个心室肌细胞去极化过程中,反向模式钠钙交换和L型钙电流(ICaL)触发的钙离子释放特性(全细胞电压钳,用Fluo 3和fura红作为细胞内钙离子指示剂,36±1℃,含20 mmol/L[Na+]的基于钾的电极内液)。向+60 mV的预处理脉冲可确保肌浆网有相当的钙离子负载。在存在ICaL的情况下,细胞内钙离子瞬变通常有一个早期快速上升阶段,反映钙离子释放,其电压依赖性呈钟形,在+10 mV处达到峰值。仅通过钠钙交换体的钙离子内流(20 μmol/L尼索地平)时,肌浆网的钙离子释放通量降低,且与去极化步骤的幅度直接相关。钙离子释放之前有一个显著延迟(在+20 mV时为81±21 ms,在+70 mV时为24±4 ms),这与通过交换体的钙离子内流有关。触发释放会中断钙离子内流,交换体电流的反转证明了这一点。在高于+40 mV的电位下,根据外向交换电流计算出的通过钠钙交换体的钙离子内流幅度与ICaL相当,但反向模式钠钙交换引起的钙离子释放仍有显著延迟。我们将触发效率计算为钙离子最大释放速率与此次释放之前的钙离子内流之比;反向模式钠钙交换的效率约为ICaL的四分之一。当同时存在ICaL和反向模式钠钙交换时,钙离子释放由ICaL触发,在低于+60 mV的电位下未检测到反向模式钠钙交换对触发的贡献。反向模式钠钙交换的这些特性表明,其在动作电位期间作为钙离子释放触发因素的作用可能微不足道。