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乙醇对大鼠蓝斑神经元兴奋性氨基酸受体和烟碱型乙酰胆碱受体的抑制作用。

Inhibition by ethanol of excitatory amino acid receptors and nicotinic acetylcholine receptors at rat locus coeruleus neurons.

作者信息

Fröhlich R, Patzelt C, Illes P

机构信息

Pharmakologisches Institut der Universität, Freiburg, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1994 Dec;350(6):626-31. doi: 10.1007/BF00169367.

DOI:10.1007/BF00169367
PMID:7535898
Abstract

The frequency of spontaneous action potentials of locus coeruleus (LC) neurons was recorded extracellularly in pontine slices of the rat brain. Ethanol (1-100 mM) elevated the firing rate in most neurons; this effect was concentration-dependent. (S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA; 0.03-1 microM), kainate (0.1-3 microM), N-methyl-D-aspartate (NMDA; 1-30 microM), substance P (0.01-1 microM), nicotine (0.1-10 microM) and alpha,beta-methylene ATP (alpha,beta-meATP; 0.3-30 microM), all increased the firing. Application of ethanol (10-100 mM) to the superfusion medium for 10 min, reproducibly and concentration-dependently inhibited the facilitatory effect of NMDA (10 microM). However, the inhibitory effect of ethanol (100 mM) decreased during a 30-min superfusion period and after the wash-out of ethanol the sensitivity of LC neurons to NMDA (10 microM) tended to overshoot above their initial level. Although NMDA was more potent in the absence than in the presence of external Mg2+, ethanol (100 mM) continued to depress the facilitatory effect of a low concentration of NMDA (3 microM) in a Mg(2+)-free medium. By contrast, in a medium containing normal Mg2+, ethanol (100 mM) failed to significantly interfere with the increase in firing rate induced by a high concentration of NMDA (30 microM). The effects of kainate (0.5 microM), AMPA (0.3 microM) and nicotine (1 microM) were also depressed by ethanol (100 mM), while the effects of substance P (0.03 microM) and alpha,beta-meATP (30 microM) were not changed.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠脑桥切片中,细胞外记录蓝斑(LC)神经元的自发放电动作电位频率。乙醇(1 - 100 mM)使大多数神经元的放电频率升高;这种效应呈浓度依赖性。(S)-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA;0.03 - 1 μM)、海人酸(0.1 - 3 μM)、N-甲基-D-天冬氨酸(NMDA;1 - 30 μM)、P物质(0.01 - 1 μM)、尼古丁(0.1 - 10 μM)和α,β-亚甲基ATP(α,β-meATP;0.3 - 30 μM)均增加放电。将乙醇(10 - 100 mM)应用于灌注培养基10分钟,可重复性地且浓度依赖性地抑制NMDA(10 μM)的促进作用。然而,在30分钟的灌注期内,乙醇(100 mM)的抑制作用减弱,且在乙醇洗脱后,LC神经元对NMDA(10 μM)的敏感性倾向于超过其初始水平。尽管在无细胞外Mg2+时NMDA比有Mg2+时更有效,但乙醇(100 mM)在无Mg2+培养基中仍继续抑制低浓度NMDA(3 μM)的促进作用。相比之下,在含有正常Mg2+的培养基中,乙醇(100 mM)未能显著干扰高浓度NMDA(30 μM)诱导的放电频率增加。乙醇(百毫克)也抑制了海人酸(0.5 μM)、AMPA(0.3 μM)和尼古丁(1 μM)的作用,而P物质(0.03 μM)和α,β-meATP(30 μM)的作用未改变。(摘要截断于250字)

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