Maddison P, Newsom-Davis J, Mills K R
University Department of Clinical Neurology, Radcliffe Infirmary, Oxford, United Kingdom.
Muscle Nerve. 1998 Sep;21(9):1196-8. doi: 10.1002/(sici)1097-4598(199809)21:9<1196::aid-mus11>3.0.co;2-q.
3,4-Diaminopyridine (3,4-DAP) is known to be beneficial in the symptomatic treatment of the Lambert-Eaton myasthenic syndrome (LEMS). The effects of 3,4-DAP on the decay of postexercise augmentation were observed in 6 patients with LEMS. After 10 s maximal voluntary contraction, the amplitude of the compound muscle action potential (CMAP) recorded from abductor digiti minimi decayed exponentially after an initial rise. The rate of decay in CMAP amplitude was increased after treatment with 3,4-DAP, suggesting that this drug has an effect on the efflux of calcium ions from the presynaptic nerve terminal.
已知3,4 - 二氨基吡啶(3,4 - DAP)对兰伯特 - 伊顿肌无力综合征(LEMS)的症状治疗有益。在6例LEMS患者中观察了3,4 - DAP对运动后增强衰减的影响。在进行10秒最大自主收缩后,从小指展肌记录的复合肌肉动作电位(CMAP)幅度在最初上升后呈指数衰减。用3,4 - DAP治疗后,CMAP幅度的衰减速率增加,表明该药物对突触前神经末梢钙离子的外流有影响。