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

机译:模式切换表征了从大鼠皮质融合神经末梢记录的大电导钾通道的活性

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class="enumerated" style="list-style-type:decimal">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.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.Mode 1 activity was voltage independent although depolarization increased mode 2 channel activity. Global average channel activity was voltage and Ca2+ dependent.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.Internal application of tetraethylammonium blocked BK channel activity in a manner identical to that reported for BKCa channels.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.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 大鼠皮层融合神经末梢的由内而外的记录表明,观察到的最常见的通道是大电导K + (BK)通道,其特性与常规细胞体钙激活BK(BKCa)通道不同。 BK通道在低(模式1)和高(模式2)活动之间显示模式切换,这种效果不受膜电压的影响。内部Ca 2 + 浓度的增加与应用蛋白激酶A的方式一样,增加了在模式2中花费的时间,这种作用不能被蛋白激酶C或蛋白激酶G模仿。 模式1的活性尽管去极化增加了模式2的通道活动,但电压无关。全局平均通道活性是电压和Ca 2 + 依赖的。 碱性磷酸酶处理使通道活性永久存在于模式2中,其中活性是电压和Ca 2+ 依赖但不受蛋白激酶A,G或C的影响。 内部应用四乙铵以与报道的BKCa通道相同的方式阻断了BK通道的活性。 这些结果表明,神经末梢膜具有较大的电导K + 通道,与其他神经元制剂的BKCa通道相比,门控动力学和活性调节存在显着差异。 BK通道亚型可能起特定于神经末梢的独特生理作用。

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