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苯妥英对大鼠神经母细胞瘤细胞中延迟整流钾通道的抑制作用。

Inhibition of delayed rectifier K+ channels by phenytoin in rat neuroblastoma cells.

作者信息

Nobile M, Vercellino P

机构信息

Istituto di Cibernetica e Biofisica, CNR, Genova, Italy.

出版信息

Br J Pharmacol. 1997 Feb;120(4):647-52. doi: 10.1038/sj.bjp.0700969.

Abstract
  1. The action of the anticonvulsant drug phenytoin on K+ currents was investigated in neuroblastoma cells by whole-cell voltage-clamp recording. 2. Neuroblastoma cells expressed an outward K+ current with a voltage- and time-dependence which resembled the delayed-rectifier K+ current found in other cells. When added to the standard external solution at concentrations ranging between 1 and 200 microM, phenytoin reduced the current (n = 65). Inhibition was concentration-dependent with a half-maximal inhibitory concentration of 30.9 +/- 0.8 microM. 3. The K+ current inhibition by phenytoin was voltage-dependent with block by phenytoin being relieved by depolarization. 4. The times taken to reach steady-state inhibition and complete recovery from inhibition were about 20 s. Neither the activation and inactivation rates of the K+ current nor the K+ channel availability were significantly altered by the blocking drug. A use-dependent block was observed at phenytoin concentrations of 10, 25 and 50 microM. 5. These results suggest that phenytoin affects K+ currents and that this effect might lead to a reduction in neuronal excitability.
摘要
  1. 通过全细胞膜片钳记录,研究了抗惊厥药物苯妥英对神经母细胞瘤细胞钾离子电流的作用。2. 神经母细胞瘤细胞表达了一种具有电压和时间依赖性的外向钾离子电流,该电流类似于在其他细胞中发现的延迟整流钾离子电流。当苯妥英以1至200微摩尔的浓度添加到标准外部溶液中时,电流减小(n = 65)。抑制作用呈浓度依赖性,半数最大抑制浓度为30.9±0.8微摩尔。3. 苯妥英对钾离子电流的抑制作用具有电压依赖性,去极化可解除苯妥英的阻断。4. 达到稳态抑制和从抑制中完全恢复所需的时间约为20秒。阻断药物对钾离子电流的激活和失活速率以及钾离子通道的可用性均无显著影响。在10、25和50微摩尔的苯妥英浓度下观察到了使用依赖性阻断。5. 这些结果表明,苯妥英会影响钾离子电流,这种影响可能导致神经元兴奋性降低。

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Inhibition of delayed rectifier K+ channels by phenytoin in rat neuroblastoma cells.
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