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Properties of a constitutively active Ca2+-permeable non-selective cation channel in rabbit ear artery myocytes

机译:组成性活性Ca2 +渗透性非选择性阳离子通道在兔耳动脉心肌细胞中的性质

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摘要

In smooth muscle, non-selective cation conductances contribute to agonist-evoked depolarisation and contraction, and in the present study using patch-pipette techniques we describe the properties of a constitutively active cation channel. With whole-cell recording in K+-free conditions, there was a spontaneous current with a reversal potential (Er) that was altered by replacement of external Na+ by an impermeant cation, but not when external Cl was replaced by an impermeant anion. The tonic cation inward current could be carried by Ca2+ ions and was greatly enhanced when the external Ca2+ concentration was reduced. In outside-out patches there was spontaneous cation channel activity that could be resolved into three conductance states of about 15, 25 and 40 pS, all with the same Er as the whole-cell current. Kinetic analysis revealed that there were two open times of about 1 and 5 ms and that the currents displayed bursting kinetics with burst durations of approximately 5 ms and 25 ms. Removal of external Ca2+ ions increased the probability of channel opening (Po) sixfold, which was associated with an increase in the longer burst duration. Bath application of the diacylglycerol analogue 1-oleoyl-2-acetyl-sn-glycerol increased Po, but phorbol 12,13-dibutyrate, which stimulates protein kinase C (PKC), reduced channel activity. In contrast, the PKC inhibitor chelerythrine increased the activity of channel currents. It is concluded that in rabbit ear artery myocytes there is a constitutively active Ca2+-permeable cation channel that is regulated by external Ca2+ ions and suppressed by tonic PKC activity. It is proposed that this mechanism may contribute to the resting membrane conductance and basal Ca2+ influx in this particular arterial preparation.
机译:在平滑肌中,非选择性阳离子电导有助于激动剂引起的去极化和收缩,在本研究中,使用贴片移液器技术,我们描述了组成性活性阳离子通道的性质。在无K + 的条件下进行全细胞记录时,自发电流具有一个反向电势(Er),该电流通过用不渗透物代替外部Na + 来改变阳离子,但当外部Cl -被不渗透的阴离子取代时则不会。 Ca 2 + 离子可携带强直性阳离子的内向电流,当外部Ca 2 + 的浓度降低时,通入阳离子的电流会大大增加。在由外而外的贴片中,存在自发的阳离子通道活性,可以将其解析为大约15、25和40 pS的三个电导状态,所有电导率都与全细胞电流相同。动力学分析表明,存在两个大约为1毫秒和5毫秒的断开时间,并且电流显示出爆发动力学,其爆发持续时间约为5毫秒和25毫秒。去除外部Ca 2 + 离子使通道打开(Po)的可能性增加了六倍,这与更长的脉冲持续时间增加有关。浴中二酰基甘油类似物1-油基-2-乙酰基-sn-甘油的施用增加了Po,但是佛波醇12,13-二丁酸酯刺激了蛋白激酶C(PKC),降低了通道活性。相反,PKC抑制剂白屈菜红碱增加了通道电流的活性。结论:兔耳动脉心肌细胞中存在一个组成性活性Ca 2 + 可渗透阳离子通道,该通道受外部Ca 2 + 离子调控,并受补剂PKC活性的抑制。 。有人认为这种机制可能有助于这种特定的动脉制剂中的静息膜电导和基底Ca 2 + 流入。

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