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乙酰胆碱受体通道的自发开放。

Spontaneous openings of the acetylcholine receptor channel.

作者信息

Jackson M B

出版信息

Proc Natl Acad Sci U S A. 1984 Jun;81(12):3901-4. doi: 10.1073/pnas.81.12.3901.

Abstract

Patch clamp recordings from embryonic mouse muscle cells in culture revealed spontaneous openings of the acetylcholine receptor channel in the absence of exogenously applied cholinergic agent. The conductance of the spontaneous channel currents was, within experimental error, identical with the conductance of suberyldicholine-activated channel currents. The comparison of channel conductance was made with sodium and with cesium, each at two concentrations, with the same result. Treatment of the cells with alpha-bungarotoxin blocked the spontaneous channel currents. To determine whether the spontaneous openings were caused by an endogenous agent with cholinergic activity a reactive disulfide bond near the receptor binding site was reduced with dithiothreitol and alkylated with N-ethylmaleimide. This chemical modification reduced the effectiveness with which suberyldicholine and curare activated channel currents but did not reduce the frequency of spontaneous openings. These experiments indicate that the acetylcholine receptor briefly and infrequently fluctuates into an active state in the absence of agonist. Agonist activation of the receptor presumably accelerates this spontaneously occurring process.

摘要

对培养的胚胎小鼠肌肉细胞进行膜片钳记录发现,在未施加外源性胆碱能试剂的情况下,乙酰胆碱受体通道会自发开放。自发通道电流的电导在实验误差范围内与辛二酰二胆碱激活的通道电流的电导相同。分别在两种浓度下用钠和铯进行通道电导比较,结果相同。用α-银环蛇毒素处理细胞可阻断自发通道电流。为了确定自发开放是否由具有胆碱能活性的内源性试剂引起,用二硫苏糖醇还原受体结合位点附近的一个反应性二硫键,并用N-乙基马来酰亚胺进行烷基化。这种化学修饰降低了辛二酰二胆碱和箭毒激活通道电流的效率,但并未降低自发开放的频率。这些实验表明,在没有激动剂的情况下,乙酰胆碱受体偶尔会短暂地波动到激活状态。受体的激动剂激活可能会加速这个自发发生的过程。

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