Mouzou A, Bouron A, Guillemain J, Guerrier D, Raymond G
Laboratoire de physiologie générale, Centre national de la recherche scientifique, Université de Poitiers, France.
Can J Physiol Pharmacol. 1993 Dec;71(12):889-95. doi: 10.1139/y93-135.
The effects of 50 microM LCB29 (idrocilamide) were tested on depolarization-induced and caffeine contractures of rat soleus muscle fibers. When applied intracellularly by free diffusion in cut-end voltage-clamped fibers, LCB29 decreased tension amplitude by about 25%. The same amount of inhibition by LCB29 was observed on contractures induced by 6 mM caffeine. The drug did not affect the repriming of caffeine contractures, indicating that internal recycling of calcium was not affected. The voltage-dependent inactivation of tension was facilitated by external application of LCB29. This effect was calcium dependent, so that the greater the external calcium concentration, the greater the drug effectiveness. The spontaneous relaxation of K+ contractures was also accelerated by LCB29. It is concluded that LCB29 acts intracellularly by decreasing sarcoplasmic reticulum calcium release and externally by facilitating the voltage-dependent inactivation of the voltage sensor for excitation-contraction coupling.
研究了50微摩尔LCB29(伊多西胺)对大鼠比目鱼肌纤维去极化诱导挛缩和咖啡因诱导挛缩的影响。当通过在切断端电压钳制纤维中自由扩散进行细胞内给药时,LCB29使张力幅度降低约25%。在由6毫摩尔咖啡因诱导的挛缩中观察到LCB29有相同程度的抑制作用。该药物不影响咖啡因挛缩的再激发,表明钙的内部循环未受影响。通过外部应用LCB29可促进张力的电压依赖性失活。这种作用依赖于钙,因此外部钙浓度越高,药物效果越明显。LCB29还加速了钾离子诱导挛缩的自发松弛。得出的结论是,LCB29在细胞内通过减少肌浆网钙释放起作用,在细胞外通过促进兴奋-收缩偶联电压传感器的电压依赖性失活起作用。