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在啮齿动物中,NPAS4 通过控制伏隔核中细胞类型特异性的激活平衡来支持可卡因条件性线索。

NPAS4 supports cocaine-conditioned cues in rodents by controlling the cell type-specific activation balance in the nucleus accumbens.

作者信息

Hughes Brandon W, Huebschman Jessica L, Tsvetkov Evgeny, Siemsen Benjamin M, Snyder Kirsten K, Akiki Rose Marie, Wood Daniel J, Penrod Rachel D, Scofield Michael D, Berto Stefano, Taniguchi Makoto, Cowan Christopher W

机构信息

Department of Neuroscience, Medical University of South Carolina, Charleston, SC, USA.

Department of Anesthesiology, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Nat Commun. 2024 Aug 8;15(1):5971. doi: 10.1038/s41467-024-50099-1.

Abstract

Powerful associations that link drugs of abuse with cues in the drug-paired environment often serve as prepotent relapse triggers. Drug-associated contexts and cues activate ensembles of nucleus accumbens (NAc) neurons, including D1-class medium spiny neurons (MSNs) that typically promote, and D2-class MSNs that typically oppose, drug seeking. We found that in mice, cocaine conditioning upregulated transiently the activity-regulated transcription factor, Neuronal PAS Domain Protein 4 (NPAS4), in a small subset of NAc neurons. The NPAS4+ NAc ensemble was required for cocaine conditioned place preference. We also observed that NPAS4 functions within NAc D2-, but not D1-, MSNs to support cocaine-context associations and cue-induced cocaine, but not sucrose, seeking. Together, our data show that the NPAS4+ ensemble of NAc neurons is essential for cocaine-context associations in mice, and that NPAS4 itself functions in NAc D2-MSNs to support cocaine-context associations by suppressing drug-induced counteradaptations that oppose relapse-related behaviour.

摘要

将滥用药物与药物配对环境中的线索联系起来的强大关联常常成为复发的主要触发因素。与药物相关的环境和线索会激活伏隔核(NAc)神经元集群,其中包括通常促进觅药行为的D1类中型多棘神经元(MSN)和通常抑制觅药行为的D2类MSN。我们发现,在小鼠中,可卡因条件作用会短暂上调一小部分NAc神经元中受活动调节的转录因子——神经元PAS结构域蛋白4(NPAS4)的表达。可卡因条件性位置偏爱需要NPAS4+NAc神经元集群。我们还观察到,NPAS4在NAc的D2类而非D1类MSN中发挥作用,以支持可卡因-环境关联以及线索诱导的可卡因(而非蔗糖)觅药行为。总之,我们的数据表明,NAc神经元的NPAS4+集群对于小鼠的可卡因-环境关联至关重要,并且NPAS4本身在NAc的D2-MSN中发挥作用,通过抑制与复发相关行为相反的药物诱导的适应性反应来支持可卡因-环境关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53d8/11310321/d33284dd468c/41467_2024_50099_Fig1_HTML.jpg

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