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在雄性小鼠的奖励寻求过程中,伏隔核神经元的时间动态。

Temporal dynamics of nucleus accumbens neurons in male mice during reward seeking.

机构信息

Department of Neuroscience, University of Pittsburgh, Pittsburgh, PA, 15260, USA.

Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, PA, 15213, USA.

出版信息

Nat Commun. 2024 Oct 28;15(1):9285. doi: 10.1038/s41467-024-53690-8.

DOI:10.1038/s41467-024-53690-8
PMID:39468146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11519475/
Abstract

The nucleus accumbens (NAc) regulates reward-motivated behavior, but the temporal dynamics of NAc neurons that enable "free-willed" animals to obtain rewards remain elusive. Here, we recorded Ca activity from individual NAc neurons when mice performed self-paced lever-presses for sucrose. NAc neurons exhibited three temporally-sequenced clusters, defined by times at which they exhibited increased Ca activity: approximately 0, -2.5 or -5 sec relative to the lever-pressing. Dopamine D1 receptor (D1)-expressing neurons and D2-neurons formed the majority of the -5-sec versus -2.5-sec clusters, respectively, while both neuronal subtypes were represented in the 0-sec cluster. We found that pre-press activity patterns of D1- or D2-neurons could predict subsequent lever-presses. Inhibiting D1-neurons at -5 sec or D2-neurons at -2.5 sec, but not at other timepoints, reduced sucrose-motivated lever-pressing. We propose that the time-specific activity of D1- and D2-neurons mediate key temporal features of the NAc through which reward motivation initiates reward-seeking behavior.

摘要

伏隔核(NAc)调节奖赏驱动行为,但奖赏动机动物获得奖赏时 NAc 神经元的时间动态仍然难以捉摸。在这里,当小鼠自行按压杠杆获取蔗糖时,我们记录了单个 NAc 神经元的 Ca 活性。NAc 神经元表现出三个时间顺序排列的簇,其特征是它们表现出 Ca 活性增加的时间:相对于杠杆按压,大约为 0、-2.5 或-5 秒。多巴胺 D1 受体(D1)表达神经元和 D2 神经元分别形成了大多数-5 秒与-2.5 秒簇,而这两种神经元亚型都存在于 0 秒簇中。我们发现,D1 或 D2 神经元的预按压活动模式可以预测随后的杠杆按压。在-5 秒抑制 D1 神经元或在-2.5 秒抑制 D2 神经元,但不在其他时间点抑制,会减少蔗糖动机的杠杆按压。我们提出,D1 和 D2 神经元的时间特异性活动通过 NAc 介导奖赏动机启动奖赏寻求行为的关键时间特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/4783b7cd0b47/41467_2024_53690_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/be51a9ffad60/41467_2024_53690_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/deb17bb32607/41467_2024_53690_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/faf259fb42c6/41467_2024_53690_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/4783b7cd0b47/41467_2024_53690_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/be51a9ffad60/41467_2024_53690_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/deb17bb32607/41467_2024_53690_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/faf259fb42c6/41467_2024_53690_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7d/11519475/4783b7cd0b47/41467_2024_53690_Fig4_HTML.jpg

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