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[阿片类药物和内源性肽对中枢神经元的电生理作用]

[Electrophysiological effects of opiates and endogenous peptides on central neurons].

作者信息

Davies J

出版信息

Ann Anesthesiol Fr. 1978;19(5):399-405.

PMID:29535
Abstract

The influence of micro-iontophoretically administered opiates and opiate peptides on the activity of single neurones in the central nervous system will be discussed. It will be shown that in single neurone studies in several different supraspinal regions opiates and opiate peptides have similar actions on individual neurones and both may excite or depress neuronal activity. The excitatory and inhibitory effects of these substances can be reversed by a necrotic antagonist and therefore may be mediated via an action at specific opiate receptors. Studies on spinal neurons indicate that the excitatory action of morphine and enkephalin may be due to an interaction with a cholinergic receptor or at least cholinoceptive neurones. Evidence will also be presented showing that responses of dorsal horn neurones to nowious peripheral stimuli may be selectively reduced by morphine and enkephalin administered into the substantia gelatinosa region or the spinal cord. The relevance of these observations to the pharmacological action of opiates and the possible physiological function of endogenous opiate peptides will be mentioned.

摘要

本文将讨论经微量离子透入法给予阿片类药物和阿片肽对中枢神经系统单个神经元活动的影响。研究表明,在几个不同的脊髓上区域进行的单个神经元研究中,阿片类药物和阿片肽对单个神经元具有相似的作用,二者均可兴奋或抑制神经元活动。这些物质的兴奋和抑制作用可被坏死性拮抗剂逆转,因此可能是通过作用于特定的阿片受体介导的。对脊髓神经元的研究表明,吗啡和脑啡肽的兴奋作用可能是由于与胆碱能受体或至少是对胆碱敏感的神经元相互作用所致。还将提供证据表明,注入脊髓胶状质区域或脊髓的吗啡和脑啡肽可选择性降低背角神经元对有害外周刺激的反应。将提及这些观察结果与阿片类药物药理作用以及内源性阿片肽可能的生理功能的相关性。

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