Marchetti C, Robello M
Istituto di Cibernetica e Biofisica, Consiglio Nazionale delle Ricerche, Genova, Italy.
Biophys J. 1989 Dec;56(6):1267-72. doi: 10.1016/S0006-3495(89)82774-2.
Internal perfusion with the G-protein activator guanosine-5'-O-(3-thiotriphosphate) (GTP-gamma S) mimics the effect of noradrenaline and dopamine on the voltage-dependent calcium current in chick dorsal root ganglion (DRG) cells. With 100 microM GTP-gamma S in the pipette, the current at +10 mV was depressed by approximately 50%, with a 10-fold increase of its time to peak. The activation time course of the control calcium current could be approximated with a single exponential curve, whereas with GTP-gamma S the activation time course was double exponential, with time constants tau 1 and tau 2. 2 mM Mg-ATP in the pipette prevented the GTP-gamma S-induced current decrease in 70% of the cells, but the time course of the current was always double exponential. From -50 mV, the current at +10 mV was best fitted with tau 1 = 1.7 +/- 0.5 and tau 2 = 25.6 +/- 5.5 in seven cells. Both time constants decreased with increasing depolarizations. In the first 2 min of recording, the current changed with time. However, both tau 1 and tau 2 were constant, whereas the relative contribution of the slow component increased from 10 to 70%. In addition, the effect was independent of the holding potential in the range from -100 to -30 mV. These results suggest that the activation of a G-protein causes a fraction of the high-threshold calcium channels to switch to a new closed state, with slower opening kinetics.
用G蛋白激活剂鸟苷-5'-O-(3-硫代三磷酸)(GTP-γS)进行细胞内灌注,可模拟去甲肾上腺素和多巴胺对鸡背根神经节(DRG)细胞电压依赖性钙电流的作用。移液管中加入100μM GTP-γS时,+10mV处的电流降低约50%,其峰值时间增加了10倍。对照钙电流的激活时间进程可用单指数曲线近似,而加入GTP-γS后,激活时间进程为双指数,具有时间常数τ1和τ2。移液管中加入2mM Mg-ATP可在70%的细胞中阻止GTP-γS诱导的电流降低,但电流的时间进程始终为双指数。在-50mV时,七个细胞中+10mV处的电流最佳拟合为τ1 = 1.7±0.5和τ2 = 25.6±5.5。两个时间常数均随去极化增加而降低。在记录的前2分钟内,电流随时间变化。然而,τ1和τ2均保持不变,而慢成分的相对贡献从10%增加到70%。此外,该效应在-100至-30mV的保持电位范围内与保持电位无关。这些结果表明,G蛋白的激活会导致一部分高阈值钙通道转换为新的关闭状态,其开放动力学较慢。