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干扰素作为一种预防和减轻阿片类药物成瘾的内源性类物质候选物。

Interferon as an endocoids candidate preventing and attenuating opiate addiction.

作者信息

Dafny N

出版信息

Prog Clin Biol Res. 1985;192:269-76.

PMID:4080713
Abstract

Morphine exert numerous effects of all levels of the central nervous system with tolerance, physical dependence and withdrawal being characteristic of this drug class. The degree of dependence is directly correlated to the intensity of withdrawal, success in modifying the withdrawal syndrome may shed light on the dynamic of morphine addiction. The present study demonstrated that alpha-interferon (IFN) significantly modifies the naloxone-induced abstinence syndrome in morphine dependent rats. Single cortical neurons recording and microiontophoretic application of IFN, morphine and naloxone failed to support existing hypothesis that IFN effects are mediated through opiate receptors. Since IFN's are widely present in animals bodies, including the brain, and are locally synthesized. Our observation suggests that IFN's are endocoids which serve to prevent tolerance and dependence to endogenous peptides.

摘要

吗啡对中枢神经系统的各个层面都有众多影响,耐受性、身体依赖性和戒断是这类药物的特征。依赖程度与戒断强度直接相关,成功改变戒断综合征可能有助于揭示吗啡成瘾的机制。本研究表明,α-干扰素(IFN)能显著改变吗啡依赖大鼠中纳洛酮诱导的戒断综合征。对单个皮层神经元进行记录以及对干扰素、吗啡和纳洛酮进行微量离子电泳应用,均未能支持现有的假说,即干扰素的作用是通过阿片受体介导的。由于干扰素广泛存在于动物体内,包括大脑,并且是在局部合成的。我们的观察表明,干扰素是内源性物质,其作用是防止对内源性肽产生耐受性和依赖性。

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