Nucleus accumbens neuronal ensembles vary with cocaine reinforcement in male and female rats

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bo W. Sortman, Samantha Rakela, Sarah Paprotna, Berk Cerci, Brandon L. Warren
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Abstract

Neuronal ensembles in the medial prefrontal cortex mediate cocaine self-administration via projections to the nucleus accumbens. We have recently shown that neuronal ensembles in the prelimbic cortex form rapidly to mediate cocaine self-administration. However, the role of neuronal ensembles within the nucleus accumbens in initial cocaine-seeking behaviour remains unknown. Here, we sought to expand the current literature by testing the necessity of the cocaine self-administration ensemble in the nucleus accumbens core (NAcCore) 1 day after male and female rats acquire cocaine self-administration by using the Daun02 inactivation procedure. We found that disrupting the NAcCore ensembles after a no-cocaine reward-seeking test increased subsequent cocaine seeking, while disrupting NAcCore ensembles following a cocaine self-administration session decreased subsequent cocaine seeking. We then characterized neuronal cell type in the NAcCore using RNAscope in situ hybridization. In the no-cocaine session, we saw reduced dopamine D1 type neuronal activation, while in the cocaine self-administration session, we found preferential dopamine D1 type neuronal activity in the NAcCore.

Abstract Image

雄性和雌性大鼠的凹凸核神经元群随可卡因强化而变化
内侧前额叶皮层的神经元集合通过向阿库仑核的投射介导可卡因的自我给药。我们最近的研究表明,前边缘皮层的神经元集合会迅速形成,从而介导可卡因的自我给药。然而,在最初的可卡因觅药行为过程中,脑核内的神经元集合所起的作用仍然未知。在此,我们试图通过使用Daun02失活程序,在雄性和雌性大鼠获得可卡因自我给药1天后,测试可卡因自我给药组合在可卡因累加核核心(NAcCore)的必要性,从而扩展目前的文献。我们发现,在无可卡因奖赏寻求测试后破坏NAcCore集合会增加随后的可卡因寻求,而在可卡因自我给药后破坏NAcCore集合会减少随后的可卡因寻求。随后,我们利用RNAscope原位杂交技术确定了NAcCore的神经细胞类型。在不使用可卡因的情况下,我们发现多巴胺D1型神经元的激活减少了,而在可卡因自我给药的情况下,我们发现NAcCore中的多巴胺D1型神经元更活跃。
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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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