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[洛普明的脑电图效应]

[Electroencephalographic effects of lopramine].

作者信息

Watanabe S, Ueki S, Kawasaki H

出版信息

Nihon Yakurigaku Zasshi. 1976 Mar;72(2):153-68. doi: 10.1254/fpj.72.153.

Abstract

Electroencephalographic (EEG) effects of lopramine, a new antidepressant, were investigated in rabbits with chronic electrode implants, and compared with those of imipramine and amitriptyline. All drugs were administered i.v. Lopramine (10, 20 mg/kg) induced a drowsy pattern of spontaneous EEG consisted of high voltage slow waves in the cortex and amygdala, and desynchronization of hippocampal thetha waves. Imipramine and amitriptyline (1-5 mg/kg) also elicited similar EEG changes but were much more potent than lopramine in this effect. Lopramine (10, 20 mg/kg) failed to suppress the EEG arousal responses induced by not only auditory stimulation but also electrical stimulation of the mesencephalic reticular formation, centromedian thalamus and posterior hypothalamus, whereas imipramine and amitriptyline (1 approximately 5 mg/kg) markedly inhibited these responses. The EEG arousal response induced by i.v. injection of physostigmine 0.1 mg/kg showed no change after lopramine (20 mg/kg), while the response was significantly suppressed by imipramine (2, 5 mg/kg) and amitriptyline (1, 2 mg/kg). Lopramine showed no effect on the recruiting response induced by electrical stimulation (8 Hz) of the centromedian thalamus and slightly enhanced the limbic afterdischarges elicited by either hippocampal or amygdaloid stimulation, while imipramine (2, 5 mg/kg) and amitriptyline (1--5 mg/kg) caused an initial depression followed by sustained enhancement of these afterdischarges. These results demonstrate lopramine to be an antidepressant of a new type which has no effect on the ascending reticular activating system and no central anticholinergic action.

摘要

在慢性植入电极的家兔中研究了新型抗抑郁药洛普明的脑电图(EEG)效应,并与丙咪嗪和阿米替林的效应进行了比较。所有药物均静脉注射。洛普明(10、20mg/kg)可诱导自发EEG出现嗜睡模式,表现为皮质和杏仁核中的高电压慢波以及海马θ波的去同步化。丙咪嗪和阿米替林(1-5mg/kg)也引起类似的EEG变化,但在该效应中比洛普明更有效。洛普明(10、20mg/kg)不仅不能抑制由听觉刺激引起的EEG觉醒反应,也不能抑制中脑网状结构、丘脑中央中核和下丘脑后部的电刺激所引起的EEG觉醒反应,而丙咪嗪和阿米替林(1-5mg/kg)则明显抑制这些反应。静脉注射0.1mg/kg毒扁豆碱所诱导的EEG觉醒反应在给予洛普明(20mg/kg)后无变化,而丙咪嗪(2、5mg/kg)和阿米替林(1、2mg/kg)则可显著抑制该反应。洛普明对丘脑中央中核电刺激(8Hz)所诱导的募集反应无影响,并且对海马或杏仁核刺激所引起的边缘后放电略有增强,而丙咪嗪(2、5mg/kg)和阿米替林(1-5mg/kg)则引起这些后放电的初始抑制,随后持续增强。这些结果表明,洛普明是一种新型抗抑郁药,对上行网状激活系统无影响,也无中枢抗胆碱能作用。

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