Redmond D E, Huang Y H
J Clin Psychiatry. 1982 Jun;43(6 Pt 2):25-9.
Studies of nonhuman primates suggested that the noradrenergic locus coeruleus (LC) may be involved as part of the neural substrate for a brain alarm function which includes attentiveness, arousal, anxiety, fear, terror, and the physiological correlates of these states. The studies compared the effects of electrical activation of tiny electrodes in the locus coeruleus with the effects of other agents and conditions which increased or decreased LC activity. The results suggested that the activation of the LC system is prevented by endogenous morphine-like substances and by opiates and that the opiate withdrawal syndrome is due to activation of this LC-noradrenergic system. Clonidine, which in low doses suppressed noradrenergic and LC activity, was therefore postulated to suppress opiate withdrawal signs and symptoms. The confirmation of this hypothesis in rats, monkeys and human subjects has added to the understanding of the mechanisms of opiate action and withdrawal.
对非人类灵长类动物的研究表明,去甲肾上腺素能蓝斑核(LC)可能作为大脑警报功能神经基质的一部分参与其中,该功能包括注意力、觉醒、焦虑、恐惧、惊恐以及这些状态的生理相关反应。这些研究比较了蓝斑核中微小电极电激活的效果与其他增加或降低LC活性的药物及条件的效果。结果表明,内源性类吗啡物质和阿片类药物可阻止LC系统的激活,且阿片类药物戒断综合征是由于该LC - 去甲肾上腺素能系统的激活所致。因此,低剂量时可抑制去甲肾上腺素能和LC活性的可乐定被推测可抑制阿片类药物戒断的体征和症状。该假设在大鼠、猴子和人类受试者中的证实增进了对阿片类药物作用和戒断机制的理解。