首页> 美国卫生研究院文献>The Journal of Neuroscience >Chronic Morphine Treatment Modulates the Extracellular Levels of Endogenous Enkephalins in Rat Brain Structures Involved in Opiate Dependence: A Microdialysis Study
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Chronic Morphine Treatment Modulates the Extracellular Levels of Endogenous Enkephalins in Rat Brain Structures Involved in Opiate Dependence: A Microdialysis Study

机译:慢性吗啡治疗可调节涉及阿片依赖性的大鼠脑结构中内源性脑啡肽的细胞外水平:微透析研究

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摘要

The endogenous opioid system is often assumed to play a role in vulnerability to drug abuse. However, controversial results have been reported regarding the levels of enkephalins or preproenkephalin in neurons of rodent brains after opiate administration. The present study was performed to determine the extracellular levels of enkephalins and its physiological antagonist cholecystokinin (CCK), usingin vivo microdialysis in freely moving rats after morphine-induced physical dependence or positive place conditioning. A large increase (340%) of Met-enkephalin was observed in the periaqueductal gray matter, a structure involved in morphine withdrawal syndrome, in morphine-dependent rats. No change in CCK immunoreactivity occurred in these conditions. Moreover, using the conditioning place preference paradigm, we observed for the first time opposite changes of enkephalin outflow in the nucleus accumbens (NAc). Thus, an increase in enkephalin levels was observed in rats placed in the drug-associated compartment and a decrease in the saline-paired side. These changes in opioid peptides in the NAc may reflect an “emotional state” of the animals in relation to the expectation of drug reward (reinforcing effects of morphine). Moreover, the lack of regulation in CCK outflow suggests that CCK–opioid interactions in morphine dependence involve probably post-receptor events.
机译:通常认为内源性阿片样物质系统在药物滥用易感性中起作用。然而,关于鸦片给药后啮齿动物大脑神经元中脑啡肽或前脑啡肽的水平,有争议的结果已有报道。本研究是通过在吗啡诱导的身体依赖性或阳性位置调节后自由移动的大鼠体内进行体内微透析来确定脑啡肽及其生理拮抗剂胆囊收缩素(CCK)的细胞外水平。在吗啡依赖性大鼠中,水周周灰质(参与吗啡戒断综合征的一种结构)中的Met-脑啡肽大量增加(340%)。在这些条件下,CCK免疫反应性没有变化。此外,使用条件位置偏好范式,我们首次观察到伏伏核(NAc)中脑啡肽流出的相反变化。因此,在放置在药物相关隔室中的大鼠中观察到脑啡肽水平的增加,而在盐水配对侧的大鼠中脑啡肽水平的降低。 NAc中阿片样物质肽的这些变化可能反映了与预期的药物报酬(吗啡的增强作用)有关的动物“情绪状态”。此外,CCK流出缺乏调控提示吗啡依赖性的CCK-阿片类药物相互作用可能涉及受体后事件。

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