Delbono O, Kotsias B A
Laboratorio de Neurofisiología, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires, Argentina.
Pflugers Arch. 1987 Nov;410(4-5):394-400. doi: 10.1007/BF00586516.
The aim of this work was to study the electrical and mechanical properties of small bundles of rat diaphragm muscle treated with two blockers of the delayed potassium rectification channels: 3,4-diaminopyridine (3,4-DAP, 2.5 mM) and tetraethylammonium (TEA, 20 mM). Twitch tension was significantly potentiated by TEA and 3,4-DAP (39% and 59% respectively). Maximal tetanic tension was not affected by both drugs. The voltage dependence of the tension vs the resting membrane potential was shifted to lower values in TEA and 3,4-DAP. 3,4-DAP increased the caffeine contracture tension (2.5-10 mM) and lowered the caffeine contracture threshold. The duration of the action potential (measured at the level of -40 mV) was increased by TEA and 3,4-DAP solutions. This change was a consequence of the decrease in the rate of repolarization of the action potential. In addition, TEA reduced the amplitude and the rate of rise of the action potential. We suggested that the increment in the duration of the action potential and the shift of the mechanical threshold to more negative values of membrane potential might be the factors involved in the twitch potentiation induced by the TEA and 3,4-DAP solutions.
3,4-二氨基吡啶(3,4-DAP,2.5 mM)和四乙铵(TEA,20 mM)。TEA和3,4-DAP均显著增强了单收缩张力(分别为39%和59%)。两种药物均未影响最大强直张力。在TEA和3,4-DAP中,张力与静息膜电位的电压依赖性向更低值偏移。3,4-DAP增加了咖啡因挛缩张力(2.5 - 10 mM)并降低了咖啡因挛缩阈值。TEA和3,4-DAP溶液增加了动作电位的持续时间(在 - 40 mV水平测量)。这种变化是动作电位复极化速率降低的结果。此外,TEA降低了动作电位的幅度和上升速率。我们认为动作电位持续时间的增加以及机械阈值向更负的膜电位值的偏移可能是TEA和3,4-DAP溶液诱导单收缩增强的相关因素。