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苯妥英钠在神经肌肉接头处的突触前和突触后抑制作用。

Presynaptic and postsynaptic depressant effects of phenytoin sodium at the neuromuscular junction.

作者信息

Gage P W, Lonergan M, Torda T A

出版信息

Br J Pharmacol. 1980 May;69(1):119-21. doi: 10.1111/j.1476-5381.1980.tb10890.x.

Abstract
  1. Phenytoin sodium, 10 micrograms/ml (3.6 x 10(-5) M), reduces the amplitude of endplate potentials in mouse sternomastoid neuromuscular junctions. 2. The reduction in amplitude is due to a reduction both in the quantal content of endplate potentials and in the amplitude of the voltage response to quanta of acetylcholine. 3. The reduction caused by phenytoin in the amplitude of spontaneous miniature end plate potentials was due to a reduction in the time constant of decay of miniature endplate currents. 4. It is concluded that phenytoin depresses neuromuscular transmission by reducing both the amount of acetylcholine secreted in response to an action potential and by reducing the lifetime of postsynaptic channels activated by acetylcholine.
摘要
  1. 苯妥英钠,10微克/毫升(3.6×10⁻⁵摩尔/升),可降低小鼠胸锁乳突肌神经肌肉接头处终板电位的幅度。2. 幅度降低是由于终板电位的量子含量以及对乙酰胆碱量子的电压反应幅度均降低所致。3. 苯妥英钠引起的自发性微小终板电位幅度降低是由于微小终板电流衰减时间常数减小所致。4. 得出的结论是,苯妥英钠通过减少动作电位引发分泌的乙酰胆碱量以及缩短乙酰胆碱激活的突触后通道寿命来抑制神经肌肉传递。

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