Thomas K L, Everitt B J
Department of Experimental Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom.
J Neurosci. 2001 Apr 1;21(7):2526-35. doi: 10.1523/JNEUROSCI.21-07-02526.2001.
We investigated the neuronal activation associated with reexposure to a discrete cocaine-associated stimulus using in situ hybridization to quantify the expression of the plasticity-regulated gene, gamma protein kinase C (gamma PKC), in the limbic-cortical-ventral striatal system. Groups of rats were trained to self-administer cocaine paired with a light stimulus (Paired) or paired with an auditory stimulus but also receiving light presentations yoked to those in the Paired group (Unpaired). Additional groups received noncontingent cocaine-light pairings (Pavlovian) or saline-light pairings (Saline) that were yoked to the Paired group. After acquisition of self-administration by the Paired and Unpaired groups, all groups had a 3 d drug- and training-free period before being reexposed to noncontingent presentations of the light conditioning stimulus during a 5 min test session in the training context. There were four major patterns of results for regional gamma PKC expression 2 hr later. (1) Changes occurred only in groups in which the light was predictive of cocaine. (2) Increases were seen in the amygdala, but decreases were seen in the medial prefrontal cortex. (3) No changes were seen in the hippocampus. (4) Although changes were observed in the basal and central nuclei of the amygdala and the prelimbic cortex in both the Paired and Pavlovian groups, additional changes were observed in the nucleus accumbens core, lateral amygdala, and anterior cingulate cortex in the Pavlovian group. These results suggest not only that regionally selective alterations in gamma PKC expression are an index of the retrieval of Pavlovian associations formed between a drug and a discrete stimulus, but also that a distinct neural circuitry may underlie Pavlovian stimulus-reward associations in cocaine-experienced rats.
我们使用原位杂交技术研究了与再次暴露于离散的可卡因相关刺激相关的神经元激活情况,以量化边缘 - 皮质 - 腹侧纹状体系统中可塑性调节基因γ蛋白激酶C(γPKC)的表达。将大鼠分组训练,使其自我给药可卡因,一组与光刺激配对(配对组),另一组与听觉刺激配对,但也接受与配对组中光呈现同步的光刺激(非配对组)。另外几组接受与配对组同步的非条件性可卡因 - 光配对(巴甫洛夫组)或盐水 - 光配对(盐水组)。在配对组和非配对组习得自我给药后,所有组在训练环境中进行5分钟测试期间,有3天无药物和训练期,然后再次暴露于非条件性光条件刺激。2小时后,区域γPKC表达出现了四种主要结果模式。(1)变化仅发生在光可预测可卡因的组中。(2)杏仁核中γPKC表达增加,但内侧前额叶皮质中γPKC表达减少。(3)海马体中未见变化。(4)虽然配对组和巴甫洛夫组的杏仁核基底核和中央核以及前边缘皮质均观察到变化,但巴甫洛夫组的伏隔核核心、外侧杏仁核和前扣带回皮质还观察到额外变化。这些结果不仅表明γPKC表达的区域选择性改变是药物与离散刺激之间形成的巴甫洛夫关联检索的指标,还表明在经历过可卡因的大鼠中,独特的神经回路可能是巴甫洛夫刺激 - 奖励关联的基础。