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本文引用的文献

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Characterization of the K+ current mediated by 5-HT1A receptor in the acutely dissociated rat dorsal raphe neurons.急性分离的大鼠中缝背核神经元中5-HT1A受体介导的钾电流的特性
Brain Res. 1997 Jan 16;745(1-2):283-92. doi: 10.1016/s0006-8993(96)01141-9.
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Single-channel properties of a G-protein-coupled inward rectifier potassium channel in brain neurons.脑神经元中G蛋白偶联内向整流钾通道的单通道特性
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GABAB receptor-activated inwardly rectifying potassium current in dissociated hippocampal CA3 neurons.解离海马CA3神经元中GABAB受体激活的内向整流钾电流
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The K+ channel inward rectifier subunits form a channel similar to neuronal G protein-gated K+ channel.钾离子通道内向整流亚基形成一种类似于神经元G蛋白门控钾离子通道的通道。
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Modulation of the serotonin-activated K+ channel by G protein subunits and nucleotides in rat hippocampal neurons.G蛋白亚基和核苷酸对大鼠海马神经元中5-羟色胺激活的钾通道的调节作用
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A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels.来自人类海马体的一种G蛋白激活内向整流钾通道(GIRK4)与其他GIRK通道相关联。
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Unitary properties of potassium channels activated by 5-HT in acutely isolated rat dorsal raphe neurones.急性分离的大鼠中缝背核神经元中5-羟色胺激活的钾通道的单一特性
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Whole-cell recordings of inwardly rectifying K+ currents activated by 5-HT1A receptors on dorsal raphe neurones of the adult rat.成年大鼠中缝背核神经元上5-HT1A受体激活的内向整流钾电流的全细胞记录。
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Heterologous multimeric assembly is essential for K+ channel activity of neuronal and cardiac G-protein-activated inward rectifiers.异源多聚体组装对于神经元和心脏G蛋白激活内向整流钾通道的钾离子通道活性至关重要。
Biochem Biophys Res Commun. 1995 Jul 17;212(2):657-63. doi: 10.1006/bbrc.1995.2019.
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Evidence that neuronal G-protein-gated inwardly rectifying K+ channels are activated by G beta gamma subunits and function as heteromultimers.有证据表明神经元G蛋白门控内向整流钾通道由Gβγ亚基激活并作为异源多聚体发挥作用。
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急性分离的大鼠蓝斑神经元中α2-肾上腺素能受体介导的钾电流

alpha2-Adrenoceptor-mediated potassium currents in acutely dissociated rat locus coeruleus neurones.

作者信息

Arima J, Kubo C, Ishibashi H, Akaike N

机构信息

Departments of Physiology and Psychosomatic Medicine, Faculty of Medicine, Kyushu University, Fukuoka 812-82, Japan.

出版信息

J Physiol. 1998 Apr 1;508 ( Pt 1)(Pt 1):57-66. doi: 10.1111/j.1469-7793.1998.057br.x.

DOI:10.1111/j.1469-7793.1998.057br.x
PMID:9490817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2230849/
Abstract
  1. The noradrenaline (NA)-activated response was investigated in neurones acutely dissociated from the rat locus coeruleus (LC) using nystatin-perforated, conventional whole-cell and inside-out patch recording modes under current- and voltage-clamp conditions. 2. Under current-clamp conditions, NA hyperpolarized the LC neurones, abolishing the spontaneous action potentials. In voltage-clamp studies, NA induced an inwardly rectifying K+ current (INA) in a concentration-dependent manner with a half-maximum effective concentration of 2.2 x 10(-7) M. 3. INA was mimicked by the alpha2-agonist UK14304 but was inhibited by either the alpha2B/alpha2C antagonist ARC239 or the alpha1- and alpha2B/alpha2C antagonist prazosin, suggesting the contribution of alpha2B/alpha2C adrenoceptors. 4. INA was inhibited by the intracellular application of GDPbetaS but fully activated by intracellular perfusion of GTPgammaS. 5. In the inside-out recording mode, the application of GTP to the cytoplasmic side of the patch membrane markedly enhanced the open probability of the NA-activated single channels which represented the inwardly rectifying properties. 6. These results indicate that the activation of alpha2B/alpha2C adrenoceptors coupled with GTP-binding protein directly activates the inwardly rectifying K+ currents in rat LC neurones, thus resulting in a decrease in the spontaneous firing activities.
摘要
  1. 利用制霉菌素穿孔膜片钳、传统全细胞膜片钳和内面向外膜片钳记录模式,在电流钳和电压钳条件下,对急性分离自大鼠蓝斑(LC)的神经元中去甲肾上腺素(NA)激活的反应进行了研究。2. 在电流钳条件下,NA使LC神经元超极化,消除了自发动作电位。在电压钳研究中,NA以浓度依赖性方式诱导内向整流钾电流(INA),半数最大有效浓度为2.2×10⁻⁷ M。3. INA可被α₂激动剂UK14304模拟,但被α₂B/α₂C拮抗剂ARC239或α₁及α₂B/α₂C拮抗剂哌唑嗪抑制,提示α₂B/α₂C肾上腺素能受体的作用。4. INA被细胞内应用GDPβS抑制,但被细胞内灌注GTPγS完全激活。5. 在内面向外记录模式下,向膜片膜的胞质侧施加GTP可显著提高NA激活的单通道的开放概率,该单通道表现出内向整流特性。6. 这些结果表明,α₂B/α₂C肾上腺素能受体与GTP结合蛋白偶联的激活直接激活大鼠LC神经元中的内向整流钾电流,从而导致自发放电活动减少。