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本文引用的文献

1
Modulation of TASK-1 (Kcnk3) and TASK-3 (Kcnk9) potassium channels: volatile anesthetics and neurotransmitters share a molecular site of action.TASK-1(Kcnk3)和TASK-3(Kcnk9)钾通道的调节:挥发性麻醉剂和神经递质共享一个分子作用位点。
J Biol Chem. 2002 May 17;277(20):17733-42. doi: 10.1074/jbc.M200502200. Epub 2002 Mar 8.
2
Serotonergic raphe neurons express TASK channel transcripts and a TASK-like pH- and halothane-sensitive K+ conductance.5-羟色胺能中缝神经元表达TASK通道转录本以及一种类似TASK的pH值和氟烷敏感的钾离子电导。
J Neurosci. 2002 Feb 15;22(4):1256-65. doi: 10.1523/JNEUROSCI.22-04-01256.2002.
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Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K(+) channel subunit, TASK-5, associated with the central auditory nervous system.与中枢听觉神经系统相关的TASK-1、TASK-3和串联孔结构域钾通道亚基TASK-5在大脑中的表达模式。
Mol Cell Neurosci. 2001 Dec;18(6):632-48. doi: 10.1006/mcne.2001.1045.
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Formation of functional heterodimers between the TASK-1 and TASK-3 two-pore domain potassium channel subunits.TASK-1和TASK-3两孔结构域钾通道亚基之间功能性异源二聚体的形成。
J Biol Chem. 2002 Feb 15;277(7):5426-32. doi: 10.1074/jbc.M107138200. Epub 2001 Dec 3.
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Cns distribution of members of the two-pore-domain (KCNK) potassium channel family.两孔结构域(KCNK)钾通道家族成员在中枢神经系统中的分布。
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Molecular mechanism of cAMP modulation of HCN pacemaker channels.环磷酸腺苷(cAMP)对超极化激活的环核苷酸门控(HCN)起搏通道调节的分子机制
Nature. 2001 Jun 14;411(6839):805-10. doi: 10.1038/35081088.
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Inhibition of TASK-1 potassium channel by phospholipase C.
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KT3.2 and KT3.3, two novel human two-pore K(+) channels closely related to TASK-1.KT3.2和KT3.3,两种与TASK-1密切相关的新型人类双孔钾通道。
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Increased noradrenaline release from rat preoptic area during and after sevoflurane and isoflurane anesthesia.七氟烷和异氟烷麻醉期间及之后大鼠视前区去甲肾上腺素释放增加。
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Properties of hyperpolarization-activated pacemaker current defined by coassembly of HCN1 and HCN2 subunits and basal modulation by cyclic nucleotide.由HCN1和HCN2亚基共同组装定义的超极化激活起搏电流的特性以及环核苷酸的基础调节。
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吸入性麻醉剂和神经递质对大鼠脑干运动神经元中钾离子泄漏电流和I(h)的汇聚性和相互调制作用

Convergent and reciprocal modulation of a leak K+ current and I(h) by an inhalational anaesthetic and neurotransmitters in rat brainstem motoneurones.

作者信息

Sirois Jay E, Lynch Carl, Bayliss Douglas A

机构信息

Department of Pharmacology, University of Virginia, Charlottesville 22908, USA.

出版信息

J Physiol. 2002 Jun 15;541(Pt 3):717-29. doi: 10.1113/jphysiol.2002.018119.

DOI:10.1113/jphysiol.2002.018119
PMID:12068035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2290347/
Abstract

Neurotransmitters and volatile anaesthetics have opposing effects on motoneuronal excitability which appear to reflect contrasting modulation of two types of subthreshold currents. Neurotransmitters increase motoneuronal excitability by inhibiting TWIK-related acid-sensitive K+ channels (TASK) and shifting activation of a hyperpolarization-activated cationic current (I(h)) to more depolarized potentials; on the other hand, anaesthetics decrease excitability by activating a TASK-like current and inducing a hyperpolarizing shift in I(h) activation. Here, we used whole-cell recording from motoneurones in brainstem slices to test if neurotransmitters (serotonin (5-HT) and noradrenaline (NA)) and an anaesthetic (halothane) indeed compete for modulation of the same ion channels - and we determined which prevails. When applied together under current clamp conditions, 5-HT reversed anaesthetic-induced membrane hyperpolarization and increased motoneuronal excitability. Under voltage clamp conditions, 5-HT and NA overcame most, but not all, of the halothane-induced current. When I(h) was blocked with ZD 7288, the neurotransmitters completely inhibited the K+ current activated by halothane; the halothane-sensitive neurotransmitter current reversed at the equilibrium potential for potassium (E(K)) and displayed properties expected of acid-sensitive, open-rectifier TASK channels. To characterize modulation of I(h) in relative isolation, effects of 5-HT and halothane were examined in acidified bath solutions that blocked TASK channels. Under these conditions, 5-HT and halothane each caused their characteristic shift in voltage-dependent gating of I(h). When tested concurrently, however, halothane decreased the neurotransmitter-induced depolarizing shift in I(h) activation. Thus, halothane and neurotransmitters converge on TASK and I(h) channels with opposite effects; transmitter action prevailed over anaesthetic effects on TASK channels, but not over effects on I(h). These data suggest that anaesthetic actions resulting from effects on either TASK or hyperpolarization-activated cyclic nucleotide-gated (HCN) channels in motoneurones, and perhaps at other CNS sites, can be modulated by prevailing neurotransmitter tone.

摘要

神经递质和挥发性麻醉剂对运动神经元兴奋性具有相反的作用,这似乎反映了对两种阈下电流的不同调节。神经递质通过抑制TWIK相关酸敏感钾通道(TASK)并将超极化激活阳离子电流(I(h))的激活转移到更去极化电位来增加运动神经元兴奋性;另一方面,麻醉剂通过激活一种类似TASK的电流并诱导I(h)激活的超极化偏移来降低兴奋性。在这里,我们使用脑干切片中运动神经元的全细胞记录来测试神经递质(5-羟色胺(5-HT)和去甲肾上腺素(NA))和一种麻醉剂(氟烷)是否确实竞争对相同离子通道的调节——并且我们确定了哪种作用占主导。在电流钳制条件下共同应用时,5-HT逆转了麻醉剂诱导的膜超极化并增加了运动神经元兴奋性。在电压钳制条件下,5-HT和NA克服了大部分但不是全部氟烷诱导的电流。当用ZD 7288阻断I(h)时,神经递质完全抑制了由氟烷激活的钾电流;氟烷敏感的神经递质电流在钾平衡电位(E(K))处反转,并表现出酸敏感、开放整流TASK通道预期的特性。为了相对孤立地表征I(h)的调节,在阻断TASK通道的酸化浴溶液中检查了5-HT和氟烷的作用。在这些条件下,5-HT和氟烷各自引起I(h)电压依赖性门控的特征性偏移。然而,当同时测试时,氟烷减少了神经递质诱导的I(h)激活的去极化偏移。因此,氟烷和神经递质以相反的作用汇聚在TASK和I(h)通道上;递质作用在TASK通道上胜过麻醉剂作用,但在对I(h)的作用上并非如此。这些数据表明,运动神经元中以及可能在其他中枢神经系统部位,由对TASK或超极化激活环核苷酸门控(HCN)通道的作用所产生的麻醉作用可被占主导的神经递质张力所调节。