Bird Michael K, Lohmann Peter, West Billy, Brown Robyn M, Kirchhoff Jeppe, Raymond Clarke R, Lawrence Andrew J
Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia.
The John Curtin School of Medical Research & Eccles Institute of Neuroscience, Australian National University, Canberra, Australia.
Drug Alcohol Depend. 2014 Apr 1;137:83-9. doi: 10.1016/j.drugalcdep.2014.01.017. Epub 2014 Jan 31.
There is extensive evidence implicating the metabotropic glutamate 5 (mGlu5) receptor in aspects of addiction-related behaviours.
Here, we used a well-characterized line of mGlu5-deficient mice to further examine the role of this receptor in cocaine-driven behaviours. We confirmed the previously reported deficit in hippocampal long-term potentiation and associated spatial learning impairment.
Despite a spatial learning deficit, mGlu5-deficient mice developed and maintained a conditioned place preference to cocaine, suggesting cocaine reward and Pavlovian conditioning are intact in these animals. Notably, however, mGlu5-deficient mice exhibited a marked deficit in the extinction of a cocaine-conditioned place preference compared to wild type littermates. Moreover, in a fixed ratio operant intravenous self-administration paradigm, both genotypes showed similar responding for cocaine over two different doses, while mGlu5-deficient mice displayed enhanced responding on a progressive ratio schedule. In addition, cue-induced drug-seeking after abstinence was exaggerated in mGlu5-deficient mice.
Collectively, these findings suggest that while the mGlu5 receptor may be involved in mediating the rewarding effects of cocaine, it appears necessary for the extinction of cocaine-driven behaviours.
有大量证据表明代谢型谷氨酸5(mGlu5)受体与成瘾相关行为的多个方面有关。
在此,我们使用了一种特征明确的mGlu5基因敲除小鼠品系,以进一步研究该受体在可卡因驱动行为中的作用。我们证实了先前报道的海马体长期增强作用缺陷以及相关的空间学习障碍。
尽管存在空间学习缺陷,但mGlu5基因敲除小鼠仍对可卡因产生并维持了条件性位置偏爱,这表明这些动物的可卡因奖赏和巴甫洛夫条件反射是完整的。然而,值得注意的是,与野生型同窝小鼠相比,mGlu5基因敲除小鼠在可卡因条件性位置偏爱的消退方面表现出明显缺陷。此外,在固定比率操作性静脉自我给药范式中,两种基因型在两种不同剂量的可卡因上表现出相似的反应,而mGlu5基因敲除小鼠在累进比率时间表上表现出增强的反应。另外,mGlu5基因敲除小鼠在禁欲后线索诱导的觅药行为被夸大。
总体而言,这些发现表明,虽然mGlu5受体可能参与介导可卡因的奖赏作用,但它似乎是可卡因驱动行为消退所必需的。