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Two-pore-domain potassium channels in smooth muscles: new components of myogenic regulation

机译:平滑肌中的两孔域钾离子通道:肌源性调节的新组成部分

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摘要

Gastrointestinal (GI) smooth muscles are influenced by many levels of regulation, including those provided by enteric motor neurones, hormones and paracrine substances. The integrated contractile responses to these regulatory mechanisms depend heavily on the state of excitability of smooth muscle cells. Resting ionic conductances and myogenic responses to agonists and physical parameters, such as stretch, are important in establishing basal excitability. This review discusses the role of 2-pore-domain K+ channels in contributing to background conductances and in mediating responses of GI muscles to enteric inhibitory nerve stimulation and stretch. Murine GI muscles express TREK-1 channels and display a stretch-dependent K+ (SDK) conductance that is also activated by nitric oxide via a cGMP-dependent mechanism. Cloning and expression of mTREK-1 produced an SDK conductance that was activated by cGMP-dependent phosphorylation at serine-351. GI muscle cells also express TASK-1 and TASK-2 channels that are inhibited by lidocaine and external acidification. These conductances appear to provide significant background K+ permeability that contributes to the negative resting potentials of GI muscles.
机译:胃肠道(GI)平滑肌受多种调节水平的影响,包括肠道运动神经元,激素和旁分泌物质提供的调节水平。对这些调节机制的综合收缩反应在很大程度上取决于平滑肌细胞的兴奋性状态。静息的离子电导和对激动剂和物理参数(如拉伸)的肌原性反应对于建立基础兴奋性很重要。这项审查讨论2-孔域K +通道在有助于背景电导和介导胃肠道肌肉对肠道抑制性神经刺激和伸展的反应中的作用。鼠的GI肌肉表达TREK-1通道并显示出依赖于拉伸的K +(SDK)电导,该电导也被一氧化氮通过依赖于cGMP的机制激活。 mTREK-1的克隆和表达产生了SDK电导,该电导被cGMP依赖的丝氨酸351磷酸化激活。胃肠道肌肉细胞还表达受利多卡因和外部酸化抑制的TASK-1和TASK-2通道。这些电导似乎提供了显着的背景K +渗透性,有助于GI肌肉的负静息电位。

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