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由κ阿片受体介导的拟精神病现象。

Psychotomimesis mediated by kappa opiate receptors.

作者信息

Pfeiffer A, Brantl V, Herz A, Emrich H M

出版信息

Science. 1986 Aug 15;233(4765):774-6. doi: 10.1126/science.3016896.

Abstract

The kappa opioid agonists are analgesics that seem to be free of undesired morphine-like effects. Their dysphoric actions observed with the kappa agonist cyclazocine are thought to be mediated by an action at sigma-phencyclidine receptors. The benzomorphan kappa agonist MR 2033 is inactive at sigma-phencyclidine receptors. In male subjects, the opiate-active (-)-isomer, but not the (+)-isomer, elicited dose-dependent dysphoric and psychotomimetic effects that were antagonized by naloxone. Thus, kappa opiate receptors seem to mediate psychotomimetic effects. In view of the euphorigenic properties of mu agonists, our results imply the existence of opposed opioid systems affecting emotional and perceptual experiences.

摘要

κ阿片受体激动剂是一类镇痛药,似乎没有不期望的吗啡样效应。用κ激动剂环唑辛观察到的烦躁不安作用被认为是由对σ-苯环利定受体的作用介导的。苯并吗啡烷κ激动剂MR 2033对σ-苯环利定受体无活性。在男性受试者中,具有阿片活性的(-)-异构体而非(+)-异构体引发了剂量依赖性的烦躁不安和拟精神病效应,这些效应可被纳洛酮拮抗。因此,κ阿片受体似乎介导了拟精神病效应。鉴于μ激动剂的致欣快特性,我们的结果暗示存在影响情绪和感知体验的相反阿片系统。

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