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首页> 外文期刊>Behavioural Brain Research: An International Journal >Expression of c-Fos in the rat central amygdala accompanies the acquisition but not expression of conditioned place aversion induced by withdrawal from acute morphine dependence.
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Expression of c-Fos in the rat central amygdala accompanies the acquisition but not expression of conditioned place aversion induced by withdrawal from acute morphine dependence.

机译:大鼠中部杏仁核中c-Fos的表达与急性吗啡依赖戒断引起的条件性厌恶表达有关,但与表达无关。

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摘要

Conditioned reinforcement is hypothesized to be critically involved in drug addiction as a factor contributing to compulsive drug use and relapse. The present study focused on the neurobiology involved in the acquisition and expression of conditioned reinforcing effects of morphine withdrawal employing a conditioned place aversion (CPA) paradigm in acute-dependent rats. Expression of c-Fos in the amygdala (the central nucleus, CeA; the medial nucleus, MeA; the basolateral nucleus, BLA) following naloxone-precipitated withdrawal and the CPA test was examined using a range of naloxone doses (0.02, 0.05, 0.1, 0.2, 0.5 and 1.0mg/kg). Naloxone dose-dependently produced CPA in rats given a single morphine exposure. In CeA, but not MeA with high-level constitutive neuronal activity, the naloxone-induced modification in c-Fos immunoreactivity following morphine pretreatment exhibited a dose-dependent pattern similar to that seen in the behavioral study. On the other hand, none of the three amygdaloid nuclei examined including CeA, MeA and BLA showed notable sensitivity of c-Fos to the conditioned withdrawal stimulus. These results suggest that CeA may play a role in the negative affective aspect of withdrawal from acute dependence, and in part suggest that the acquisition and expression of CPA may involve different neurobiological mechanisms.
机译:有条件的强化被认为是成瘾的关键因素,它是强迫性吸毒和复发的一个因素。本研究集中于神经生物学,涉及在急性依赖大鼠中采用条件位置避开(CPA)范例获取和表达吗啡戒断条件增强作用。纳洛酮沉淀戒断后杏仁核(中央核,CeA;内侧核,MeA;基底外侧核,BLA)中c-Fos的表达,并使用一系列纳洛酮剂量(0.02、0.05、0.1)检查了CPA测试,0.2、0.5和1.0mg / kg)。纳洛酮在单次吗啡暴露下剂量依赖性地在大鼠中产生CPA。在CeA中,但不是具有高水平组成型神经元活性的MeA中,吗啡预处理后纳洛酮诱导的c-Fos免疫反应性改变表现出与行为研究相似的剂量依赖性模式。另一方面,所检查的三个杏仁核(包括CeA,MeA和BLA)均未显示c-Fos对条件戒断刺激具有显着敏感性。这些结果表明,CeA可能在退出急性依赖的负面影响方面发挥了作用,部分表明CPA的获得和表达可能涉及不同的神经生物学机制。

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