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模式转换是大鼠皮质融合神经末梢记录到的大电导钾通道活性的特征。

Mode switching characterizes the activity of large conductance potassium channels recorded from rat cortical fused nerve terminals.

作者信息

Smith M A, Ashford M L

机构信息

Department of Biomedical Sciences, University of Aberdeen, Institute of Medical Sciences, Foresterhill, Aberdeen AB25 2ZD,, UK.

出版信息

J Physiol. 1998 Dec 15;513 ( Pt 3)(Pt 3):733-47. doi: 10.1111/j.1469-7793.1998.733ba.x.

Abstract
  1. Inside-out recordings from rat cortical fused nerve terminals indicate that the most common channel observed was a large conductance K+ (BK) channel with characteristics dissimilar to conventional cell body calcium-activated BK (BKCa) channels. 2. BK channels exhibit mode switching between low (mode 1) and high (mode 2) activity, an effect not influenced by membrane voltage. Increasing internal Ca2+ concentration increased time spent in mode 2 as did application of protein kinase A, an effect not mimicked by protein kinase C or protein kinase G. 3. Mode 1 activity was voltage independent although depolarization increased mode 2 channel activity. Global average channel activity was voltage and Ca2+ dependent. 4. Alkaline phosphatase treatment induced channel activity to reside permanently in mode 2, where activity was voltage and Ca2+ dependent but unaffected by protein kinases A, G or C. 5. Internal application of tetraethylammonium blocked BK channel activity in a manner identical to that reported for BKCa channels. 6. These results indicate that nerve terminal membranes have large conductance K+ channels with significant differences in gating kinetics and regulation of activity compared with BKCa channels of other neuronal preparations. The BK channel subtype may play a unique physiological role specific to the nerve terminal.
摘要
  1. 对大鼠皮质融合神经末梢进行的外向膜片钳记录表明,观察到的最常见通道是一种大电导钾离子(BK)通道,其特性与传统细胞体钙激活BK(BKCa)通道不同。2. BK通道在低(模式1)和高(模式2)活性之间表现出模式转换,这种效应不受膜电压影响。增加胞内钙离子浓度会增加处于模式2的时间,蛋白激酶A的应用也会产生同样的效果,而蛋白激酶C或蛋白激酶G则不会模拟这种效应。3. 模式1活性与电压无关,尽管去极化会增加模式2通道的活性。整体平均通道活性与电压和钙离子有关。4. 碱性磷酸酶处理会使通道活性永久处于模式2,在该模式下活性与电压和钙离子有关,但不受蛋白激酶A、G或C的影响。5. 胞内应用四乙铵以与报道的BKCa通道相同的方式阻断BK通道活性。6. 这些结果表明,与其他神经元制剂的BKCa通道相比,神经末梢膜具有大电导钾离子通道,其门控动力学和活性调节存在显著差异。BK通道亚型可能在神经末梢发挥独特的生理作用。

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