Sárközi S, Szentesi P, Cseri J, Kovács L, Csernoch L
Department of Physiology, University Medical School Debrecen, Hungary.
J Muscle Res Cell Motil. 1996 Dec;17(6):647-56. doi: 10.1007/BF00154059.
The effects of low (10-100 microM) concentrations of tetracaine on intermembrane charge movement and on the rate of calcium release (Rrel) from the sarcoplasmic reticulum (SR) were studied in cut skeletal muscle fibres of the frog using the voltage clamp technique. The fibres were mounted in a single or double vaseline gap chamber to study the events near the contraction threshold or in a wide membrane potential range. Although the 'hump' component of charge movement (Q gamma) was suppressed to some extent, the voltage dependence and the parameters of the Boltzmann distribution were not modified significantly at tetracaine concentrations below 50 microM. At 50 and 100 microM of tetracaine the midpoint voltage of the Boltzmann distribution was shifted to higher membrane potentials and the steepness was decreased. The total available charge remained the same at all concentrations tested. Using fura-2 to measure calcium transients at 100 microM tetracaine the threshold for calcium release was found to be significantly shifted to more positive membrane potentials. Tetracaine reversibly suppressed both the early inactivating peak and the steady-level of Rrel but the concentration dependence of the effects was markedly different. The inactivation component of calcium release was decreased with a Hill coefficient of approximately 1 and half effective concentration of 11.8 microM while the steady-level was decreased with a Hill coefficient of greater than 2 and a half effective concentration of 47.0 microM. These results favour two sites of action where tetracaine would suppress the calcium release from the SR.
利用电压钳技术,研究了低浓度(10 - 100微摩尔)丁卡因对青蛙离体骨骼肌纤维膜间电荷移动以及肌浆网(SR)钙释放速率(Rrel)的影响。将纤维置于单或双凡士林间隙室中,以研究接近收缩阈值或宽膜电位范围内的事件。尽管电荷移动的“驼峰”成分(Qγ)在一定程度上受到抑制,但在丁卡因浓度低于50微摩尔时,电压依赖性和玻尔兹曼分布参数并未显著改变。在丁卡因浓度为50和100微摩尔时,玻尔兹曼分布的中点电压向更高的膜电位移动,且陡度降低。在所有测试浓度下,总可用电荷量保持不变。使用fura - 2测量100微摩尔丁卡因时的钙瞬变,发现钙释放阈值显著向更正的膜电位移动。丁卡因可逆地抑制钙释放的早期失活峰和稳定水平,但效应的浓度依赖性明显不同。钙释放的失活成分以约1的希尔系数和11.8微摩尔的半数有效浓度降低;而稳定水平以大于2的希尔系数和47.0微摩尔的半数有效浓度降低。这些结果支持丁卡因作用于两个位点抑制肌浆网钙释放的观点。