Brănişteanu D D, Brănişteanu D D, Haulică I D
Institute of Medicine and Pharmacy, Department of Physiology, Romania.
Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):257-61. doi: 10.1007/BF00172675.
Low concentrations of procaine (10(-6)-5 X 10(-5) mol/l) induced a significant increase of the spontaneous quantal transmitter release in the neuromuscular junctions of the frog cutaneous pectoris nerve-muscle preparation. The frequency of miniature endplate potentials (mepps) was increased although their size slightly decreased probably on the account of a partial block of Na+-channels at the postsynaptic membrane. The activatory effect of pre-caine was not altered under experimental conditions known to change the Ca2+ fluxes across the nerve terminal membrane such as using a Ca2+-free Ringer, or a Ca2+-channel blocker (D600), a high K+ Ringer or, finally, a low Na+ Ringer. In the presence of caffeine no change of procaine-induced activation appeared. Trifluoperazine (TFP), in a concentration known to specifically block calmodulin, completely blocked the procaine-induced increase of mepp frequency. These data suggest that procaine presumably by way of a calmodulin-dependent mechanism is related to the free cytosolic Ca2+ equilibrium. It is possible that procaine increases the free cytosolic Ca2+ concentration by blocking an active calmodulin-dependent Ca2+ extrusion mechanism.
低浓度的普鲁卡因(10⁻⁶ - 5×10⁻⁵mol/L)可使蛙胸皮神经-肌肉标本神经肌肉接头处的自发量子递质释放显著增加。微小终板电位(mepps)的频率增加,尽管其幅度略有减小,这可能是由于突触后膜上的Na⁺通道部分受阻。在已知会改变跨神经末梢膜Ca²⁺通量的实验条件下,如使用无Ca²⁺的林格液、Ca²⁺通道阻滞剂(D600)、高K⁺林格液或低Na⁺林格液,普鲁卡因的激活作用并未改变。在咖啡因存在的情况下,普鲁卡因诱导的激活没有变化。三氟拉嗪(TFP),以已知能特异性阻断钙调蛋白的浓度,完全阻断了普鲁卡因诱导的mepp频率增加。这些数据表明,普鲁卡因可能通过一种钙调蛋白依赖性机制与游离胞质Ca²⁺平衡有关。普鲁卡因有可能通过阻断一种活跃的钙调蛋白依赖性Ca²⁺外排机制来增加游离胞质Ca²⁺浓度。