首页> 外文期刊>The European Journal of Neuroscience >Chronic morphine exposure and spontaneous withdrawal are associated with modifications of dopamine receptor and neuropeptide gene expression in the rat striatum.
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Chronic morphine exposure and spontaneous withdrawal are associated with modifications of dopamine receptor and neuropeptide gene expression in the rat striatum.

机译:慢性吗啡暴露和自发戒断与大鼠纹状体中多巴胺受体和神经肽基因表达的修饰有关。

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The influence of chronic morphine and spontaneous withdrawal on the expression of dopamine receptors and neuropeptide genes in the rat striatum was investigated. Morphine dependence was induced by subcutaneous implantation of two morphine pellets for 6 days. Rats were made abstinent by removal of the pellets 1, 2 or 3 days before they were killed. The mRNA levels coding for D1- and D2-dopamine receptors, dynorphin, preproenkephalin A and substance P were determined by quantitative in situ hybridization. The caudate putamen and the nucleus accumbens showed equivalent modifications in dopamine receptor and neuropeptide gene expression. After 6 days of morphine, a decrease in D2-dopamine receptor and neuropeptide mRNA levels was observed (-30%), but there was no change in D1-dopamine receptor mRNA. In abstinent rats, both D1- and D2-dopamine receptor mRNA levels were decreased 1 day after withdrawal (-30% compared with chronic morphine). In contrast, neuropeptide mRNA levels were unaffected when compared with those observed after 6 days of morphine. During the second and third day of withdrawal, there was a gradual return to the levels seen in the placebo-treated group, for both dopamine receptor and neuropeptide mRNAs. Phenotypical characterization of striatal neurons expressing mu and kappa opioid receptor mRNAs showed that, in striatonigral neurons, both mRNAs were colocalized with D1-receptor and Dyn mRNAs. Our results suggest that during morphine dependence, dopamine and morphine exert opposite effects on striatonigral neurons, and that effects occurring on striatopallidal neurons are under dopaminergic control. We also show that withdrawal is associated with a down regulation of the postsynaptic D1 and D2 receptors.
机译:研究了慢性吗啡和自发戒断对大鼠纹状体中多巴胺受体和神经肽基因表达的影响。通过皮下植入两个吗啡药丸6天来诱导吗啡依赖性。在处死大鼠前1、2或3天,通过除去小球使大鼠戒断。通过定量原位杂交测定编码D1-和D2-多巴胺受体,强啡肽,前脑啡肽A和P物质的mRNA水平。尾状壳核和伏隔核在多巴胺受体和神经肽基因表达中显示出相同的修饰。吗啡处理6天后,观察到D2-多巴胺受体和神经肽mRNA水平下降(-30%),但D1-多巴胺受体mRNA没有变化。在戒断大鼠中,停药后1天D1和D2多巴胺受体mRNA水平均下降(与慢性吗啡相比为-30%)。相反,与吗啡6天后观察到的相比,神经肽mRNA水平未受影响。在戒断的第二天和第三天,多巴胺受体和神经肽mRNA逐渐恢复到安慰剂治疗组的水平。表达mu和κ阿片受体mRNA的纹状体神经元的表型特征表明,在纹状体神经元中,两个mRNA均与D1受体和Dyn mRNA共定位。我们的研究结果表明,在吗啡依赖期间,多巴胺和吗啡对纹状体顶神经元具有相反的作用,而对纹状体锥体神经元的作用受到多巴胺能控制。我们还显示戒断与突触后D1和D2受体的下调有关。

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