Berridge C W, Foote S L
Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla 92093.
J Neurosci. 1991 Oct;11(10):3135-45. doi: 10.1523/JNEUROSCI.11-10-03135.1991.
Experiments were conducted to examine the hypothesis that increased neuronal discharge activity of noradrenergic neurons of the locus coeruleus (LC) above resting discharge rates can alter forebrain electroencephalographic (EEG) activity. Small infusions (70-135 nl) of the cholinergic agonist bethanechol within 500 microns of the LC were used to activate this nucleus reversibly in halothane-anesthetized rats. A combined recording-infusion probe allowed verification of this electrophysiological activation. Simultaneously, EEG activity was recorded from sites in the frontal cortex and hippocampus and subjected to power-spectrum analyses. The findings were (1) LC activation was consistently followed, within 5 to 30 sec, by a shift from low-frequency, high-amplitude to high-frequency, low-amplitude EEG activity in frontal neocortex and by the appearance of intense theta-rhythm in the hippocampus; (2) forebrain EEG changes followed LC activation with similar latencies whether infusions were made lateral or medial to the LC; (3) infusions placed outside the immediate vicinity of the LC were not followed by these forebrain EEG effects; (4) following infusion-induced activation, forebrain EEG returned to preinfusion patterns with about the same time course as the recovery of LC activity (10-20 min for complete recovery). These infusion-induced effects on EEG activity were blocked or severely attenuated by pretreatment with the alpha 2-agonist clonidine, which inhibits LC discharge and norepinephrine release, or the beta-antagonist propranolol. These observations indicate that enhanced LC discharge activity is the crucial mediating event for the infusion-induced changes in forebrain EEG activity observed under these conditions and suggest that LC activation may be sufficient to induce EEG signs of cortical and hippocampal activation.
蓝斑(LC)去甲肾上腺素能神经元的放电活动高于静息放电率时,可改变前脑脑电图(EEG)活动。在氟烷麻醉的大鼠中,在距LC 500微米范围内微量注射(70 - 135 nl)胆碱能激动剂氯贝胆碱,以可逆性激活该核团。一个联合记录-注射探针可验证这种电生理激活。同时,从额叶皮质和海马体部位记录EEG活动,并进行功率谱分析。研究结果如下:(1)LC激活后,在5至30秒内,额叶新皮质的EEG活动持续从低频、高振幅转变为高频、低振幅,海马体中出现强烈的θ节律;(2)无论向LC外侧还是内侧注射,前脑EEG变化跟随LC激活的潜伏期相似;(3)在LC紧邻区域之外进行注射,不会出现这些前脑EEG效应;(4)注射诱导激活后,前脑EEG恢复到注射前模式,恢复时间进程与LC活动恢复时间大致相同(完全恢复需10 - 20分钟)。这些注射诱导的对EEG活动的影响被α2激动剂可乐定(抑制LC放电和去甲肾上腺素释放)或β拮抗剂普萘洛尔预处理所阻断或严重减弱。这些观察结果表明,增强的LC放电活动是在这些条件下观察到的注射诱导前脑EEG活动变化的关键介导事件,并表明LC激活可能足以诱导皮质和海马体激活的EEG迹象。