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自由活动大鼠海马脑电的频谱分析:中枢活性药物的作用及其与诱发电位的关系

Spectral analysis of hippocampal EEG in the freely moving rat: effects of centrally active drugs and relations to evoked potentials.

作者信息

Leung L W

出版信息

Electroencephalogr Clin Neurophysiol. 1985 Jan;60(1):65-77. doi: 10.1016/0013-4694(85)90952-6.

DOI:10.1016/0013-4694(85)90952-6
PMID:2578356
Abstract

Hippocampal EEG signals derived from chronically implanted electrodes in the freely moving rat were recorded before and after administration of centrally acting drugs, and analyzed by power and coherence spectra. Eserine, ether or urethane induced a low frequency (3-6 c/sec) theta power and coherence peak in the immobile rat, which was sensitive to atropine or scopolamine. After phencyclidine, theta that occurred during walking (7-8 c/sec) was virtually abolished by atropine while in the normal rat, absolute theta power was not affected by atropine. The residue spectrum, defined as the EEG spectrum with the theta harmonics removed, was sensitive to centrally acting drugs. Ether, urethane and pentobarbital suppressed fast waves of 50-100 c/sec, and under some conditions, enhanced 15-50 c/sec waves. Eserine enhanced (30-60 c/sec) fast waves during walking while atropine suppressed fast waves and increased irregular slow activity (less than 30 c/sec). The main effects of drugs and behavior on the residue spectra and on the average evoked potentials following stimulation of the Schaffer collaterals could be explained by a previously proposed model (Leung 1982) which suggests a continuum of hippocampal 'activation' (tonic input) under the various conditions.

摘要

在自由活动的大鼠中,记录了长期植入电极所获取的海马脑电信号,这些信号在给予中枢作用药物前后进行采集,并通过功率谱和相干谱进行分析。毒扁豆碱、乙醚或乌拉坦在静止大鼠中诱发了低频(3 - 6次/秒)的θ波功率和相干峰,该峰对阿托品或东莨菪碱敏感。给予苯环己哌啶后,行走时出现的θ波(7 - 8次/秒)在阿托品作用下几乎消失,而在正常大鼠中,绝对θ波功率不受阿托品影响。去除θ波谐波后的脑电谱(即残余谱)对中枢作用药物敏感。乙醚、乌拉坦和戊巴比妥抑制了50 - 100次/秒的快波,在某些情况下,增强了15 - 50次/秒的波。毒扁豆碱在行走时增强了30 - 60次/秒的快波,而阿托品则抑制快波并增加了不规则慢波活动(小于30次/秒)。药物和行为对残余谱以及刺激海马Schaffer侧支后的平均诱发电位的主要影响,可以用先前提出的一个模型(Leung,1982)来解释,该模型表明在各种条件下海马存在一个“激活”(紧张性输入)的连续统。

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