Sanders Kenton M, Koh Sang Don
Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, USA.
J Physiol. 2006 Jan 1;570(Pt 1):37-43. doi: 10.1113/jphysiol.2005.098897. Epub 2005 Oct 20.
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.
胃肠道(GI)平滑肌受到多种调节水平的影响,包括由肠运动神经元、激素和旁分泌物质提供的调节。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。静息离子电导以及对激动剂和物理参数(如拉伸)的肌源性反应对于建立基础兴奋性很重要。本综述讨论了双孔结构域钾通道在促成背景电导以及介导胃肠道肌肉对肠抑制性神经刺激和拉伸反应中的作用。小鼠胃肠道肌肉表达TREK - 1通道,并表现出一种拉伸依赖性钾(SDK)电导,该电导也可通过环鸟苷酸(cGMP)依赖性机制被一氧化氮激活。mTREK - 1的克隆和表达产生了一种SDK电导,该电导在丝氨酸351处通过cGMP依赖性磷酸化被激活。胃肠道肌肉细胞还表达TASK - 1和TASK - 2通道,它们受到利多卡因和细胞外酸化的抑制。这些电导似乎提供了显著的背景钾通透性,这有助于胃肠道肌肉的负静息电位。