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5-羟色胺在丘脑底核诱导兴奋和抑制:作用于5-HT(2C)、5-HT(4)和5-HT(1A)受体。

5-Hydroxytryptamine induced excitation and inhibition in the subthalamic nucleus: action at 5-HT(2C), 5-HT(4) and 5-HT(1A) receptors.

作者信息

Stanford I M, Kantaria M A, Chahal H S, Loucif K C, Wilson C L

机构信息

School of Life and Health Sciences, Aston University, Aston Triangle, Birmingham B4 7ET, UK.

出版信息

Neuropharmacology. 2005 Dec;49(8):1228-34. doi: 10.1016/j.neuropharm.2005.09.003. Epub 2005 Oct 17.

Abstract

Extracellular single-unit recordings in mouse brain slices were used to determine the effect of exogenously applied 5-HT on STN neurones. Recordings were made from 74 STN cells which fired action potentials at a regular rate of 7.19+/-0.5 Hz. In 61 cells (82%), 5-HT application increased STN neurone firing rate (10 microM, 180+/-16.8%, n=35) with an estimated EC(50) of 5.4 microM. The non-specific 5-HT(2) receptor agonist alpha-methyl 5-HT (1-10 microM) mimicked 5-HT induced excitations (15 cells). These excitations were significantly reduced by pre-perfusion with the specific 5-HT(2C) receptor antagonist RS102221 (500 nM, 9 cells) and the 5HT(4) antagonist GR113808 (500 nM, 7 cells). In 6 cells (8%) 5-HT induced biphasic responses where excitation was followed by inhibition, while in 7 cells (9%) inhibition of firing rate was observed alone. Inhibitory responses were reduced by the 5-HT(1A) antagonist WAY100135 (1 microM, 4 cells). No inhibitory responses were observed following alpha-methyl 5-HT applications. Both the excitations and inhibitions were unaffected by picrotoxin (50 microM, n=5) and CNQX (10 microM, n=5) indicative of direct postsynaptic effects. Thus, in STN neurones, 5-HT elicits two distinct effects, at times on the same neurone, the first being an excitation which is mediated by 5-HT(2C) and 5-HT(4) receptors and the second an inhibition which is mediated by 5-HT(1A) receptors.

摘要

利用小鼠脑片的细胞外单单位记录来确定外源性应用5-羟色胺(5-HT)对丘脑底核(STN)神经元的影响。从74个以7.19±0.5赫兹的规则频率发放动作电位的STN细胞进行记录。在61个细胞(82%)中,应用5-HT增加了STN神经元的发放频率(10微摩尔,180±16.8%,n = 35),估计半数有效浓度(EC50)为5.4微摩尔。非特异性5-HT2受体激动剂α-甲基5-HT(1 - 10微摩尔)模拟了5-HT诱导的兴奋作用(15个细胞)。用特异性5-HT2C受体拮抗剂RS102221(500纳摩尔,9个细胞)和5-HT4拮抗剂GR113808(500纳摩尔,7个细胞)预灌注可显著降低这些兴奋作用。在6个细胞(8%)中,5-HT诱导双相反应,先是兴奋随后是抑制,而在7个细胞(9%)中仅观察到发放频率的抑制。5-HT1A拮抗剂WAY100135(1微摩尔,4个细胞)可降低抑制反应。应用α-甲基5-HT后未观察到抑制反应。兴奋和抑制作用均不受印防己毒素(50微摩尔,n = 5)和CNQX(10微摩尔,n = 5)的影响,表明是直接的突触后效应。因此,在STN神经元中,5-HT引发两种不同的效应,有时作用于同一神经元,第一种是由5-HT2C和5-HT4受体介导的兴奋,第二种是由5-HT1A受体介导的抑制。

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