Berridge C W, Bolen S J, Manley M S, Foote S L
Psychology Department, University of Wisconsin, Madison, Wisconsin 53706-1611, USA.
J Neurosci. 1996 Nov 1;16(21):7010-20. doi: 10.1523/JNEUROSCI.16-21-07010.1996.
The locus coeruleus (LC)-noradrenergic system modulates forebrain electroencephalographic (EEG) activity in halothane-anesthetized rat. For example, unilateral enhancement of LC neuronal activity increases cortical EEG (ECoG) and hippocampal EEG (HEEG) indices of arousal bilaterally (Berridge and Foote, 1991). Conversely, bilateral suppression of LC discharge activity increases EEG measures of sedation (Berridge, et al., 1993b). The EEG-activating effects of LC stimulation appear to involve noradrenergic beta-receptors (Berridge and Foote, 1991). Two candidate sites at which LC efferents could influence ECoG and HEEG are the medial septum/vertical limb of the diagonal band of Broca (MS) and the substantia innominata/nucleus basalis of Meynert (SI). To determine whether norepinephrine mediates such actions within either of these regions, the EEG effects of small infusions of a beta-agonist or antagonist into MS or SI were examined in halothane-anesthetized rat. Unilateral infusions (150 nl) of the beta-agonist isoproterenol (ISO) (3.75 microg, 17 nmol) into MS, but not SI (150-450 nl), elicited robust bilateral activation of ECoG and HEEG. Infusions of glutamate (0.5 microg, 3.0 nmol) into either MS or SI elicited bilateral ECoG and HEEG activation. Neither vehicle infusions into MS nor infusions of ISO into regions adjacent to MS altered forebrain EEG activity. Bilateral, but not unilateral, MS infusions of the beta-antagonist timolol (3.75 microg, 8.7 nmol) decreased EEG indices of arousal in the lightly anesthetized preparation. Power spectral analyses provided quantitative confirmation of these qualitative observations. These results indicate that under these experimental conditions, noradrenergic efferents, presumably arising from LC, modulate forebrain EEG state via actions at beta-receptors located within MS. The results presented in the accompanying report extend these observations to the unanesthetized preparation and incorporate additional measures of behavioral state.
蓝斑(LC)-去甲肾上腺素能系统可调节氟烷麻醉大鼠的前脑脑电图(EEG)活动。例如,单侧增强LC神经元活动会双侧增加皮层脑电图(ECoG)和海马脑电图(HEEG)的觉醒指标(Berridge和Foote,1991)。相反,双侧抑制LC放电活动会增加镇静的EEG指标(Berridge等人,1993b)。LC刺激对EEG的激活作用似乎涉及去甲肾上腺素能β受体(Berridge和Foote,1991)。LC传出纤维可能影响ECoG和HEEG的两个候选部位是内侧隔区/布洛卡斜带垂直支(MS)和无名质/迈内特基底核(SI)。为了确定去甲肾上腺素是否在这些区域之一内介导此类作用,在氟烷麻醉的大鼠中检查了向MS或SI小剂量注入β激动剂或拮抗剂对EEG的影响。向MS单侧注入(150 nl)β激动剂异丙肾上腺素(ISO)(3.75μg,17 nmol),而非向SI(150 - 450 nl)注入,可引起ECoG和HEEG的强烈双侧激活。向MS或SI注入谷氨酸(0.5μg,3.0 nmol)可引起双侧ECoG和HEEG激活。向MS注入溶媒或向MS相邻区域注入ISO均未改变前脑EEG活动。双侧而非单侧向MS注入β拮抗剂噻吗洛尔(3.75μg,8.7 nmol)可降低轻度麻醉制剂中的EEG觉醒指标。功率谱分析为这些定性观察提供了定量证实。这些结果表明,在这些实验条件下,推测源自LC的去甲肾上腺素能传出纤维通过作用于位于MS内的β受体来调节前脑EEG状态。随附报告中呈现的结果将这些观察扩展至未麻醉的制剂,并纳入了行为状态的其他测量指标。