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本文引用的文献

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Structure and function of two-pore-domain K+ channels: contributions from genetic model organisms.双孔结构域钾通道的结构与功能:来自遗传模式生物的贡献
Trends Pharmacol Sci. 2005 Jul;26(7):361-7. doi: 10.1016/j.tips.2005.05.003.
2
Expression of TASK and TREK, two-pore domain K+ channels, in human myometrium.双孔域钾通道TASK和TREK在人子宫肌层中的表达。
Reproduction. 2005 Apr;129(4):525-30. doi: 10.1530/rep.1.00442.
3
A pH-sensitive potassium conductance (TASK) and its function in the murine gastrointestinal tract.一种pH敏感钾离子电导(TASK)及其在小鼠胃肠道中的功能。
J Physiol. 2005 May 15;565(Pt 1):243-59. doi: 10.1113/jphysiol.2005.084574. Epub 2005 Mar 17.
4
Sulfur-containing amino acids block stretch-dependent K+ channels and nitrergic responses in the murine colon.含硫氨基酸可阻断小鼠结肠中依赖拉伸的钾离子通道和一氧化氮能反应。
Br J Pharmacol. 2005 Apr;144(8):1126-37. doi: 10.1038/sj.bjp.0706154.
5
A phospholipid sensor controls mechanogating of the K+ channel TREK-1.一种磷脂传感器控制钾离子通道TREK-1的机械门控。
EMBO J. 2005 Jan 12;24(1):44-53. doi: 10.1038/sj.emboj.7600494. Epub 2004 Dec 2.
6
The lipid-activated two-pore domain K+ channel TREK-1 is resistant to hypoxia: implication for ischaemic neuroprotection.脂质激活的双孔结构域钾通道TREK-1对缺氧具有抗性:对缺血性神经保护的意义。
J Physiol. 2005 Jan 1;562(Pt 1):213-22. doi: 10.1113/jphysiol.2004.077503. Epub 2004 Oct 21.
7
The TREK K2P channels and their role in general anaesthesia and neuroprotection.TREK钾通道蛋白2(K2P)通道及其在全身麻醉和神经保护中的作用。
Trends Pharmacol Sci. 2004 Nov;25(11):601-8. doi: 10.1016/j.tips.2004.09.003.
8
Heterogeneous expression of tandem-pore K+ channel genes in adult and embryonic rat heart quantified by real-time polymerase chain reaction.
Clin Exp Pharmacol Physiol. 2004 Mar;31(3):174-8. doi: 10.1111/j.1440-1681.2004.03964.x.
9
Fatty acid-sensitive two-pore domain K+ channels.脂肪酸敏感的双孔结构域钾通道
Trends Pharmacol Sci. 2003 Dec;24(12):648-54. doi: 10.1016/j.tips.2003.10.008.
10
Two-pore domain K channel, TASK-1, in pulmonary artery smooth muscle cells.肺动脉平滑肌细胞中的双孔结构域钾通道TASK-1
Circ Res. 2003 Nov 14;93(10):957-64. doi: 10.1161/01.RES.0000099883.68414.61. Epub 2003 Oct 9.

平滑肌中的双孔结构域钾通道:肌源性调节的新组分

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

作者信息

Sanders Kenton M, Koh Sang Don

机构信息

Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, USA.

出版信息

J Physiol. 2006 Jan 1;570(Pt 1):37-43. doi: 10.1113/jphysiol.2005.098897. Epub 2005 Oct 20.

DOI:10.1113/jphysiol.2005.098897
PMID:16239268
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1464292/
Abstract

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.

摘要

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。