奖励预期和接收对伏隔区D1+和D2+神经元的峰值调节有差异。

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Biology Pub Date : 2025-03-24 Epub Date: 2025-02-27 DOI:10.1016/j.cub.2025.02.007
T W Faust, A Mohebi, J D Berke
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引用次数: 0

摘要

伏隔核(NAc)帮助控制追求奖励的动机。两组不同的NAc投射神经元——表达多巴胺D1和D2受体——被认为分别促进和抑制动机行为。然而,对这一概念框架的支持是有限的:特别是,在动机行为期间这些不同细胞类型的尖峰模式在很大程度上是未知的。利用光遗传学标记技术,我们记录了在不受约束的大鼠执行一项操作性任务时,开始工作的动机与最近的奖励率有关,并记录了NAc核心中识别的D1+和D2+神经元的峰值。当大鼠开始试验时,D1+神经元优先增加放电,当奖励期望更高时,放电更多。相比之下,D2+细胞在试验后期优先增加放电,特别是在对奖励的反应中——这是目前理论模型没有预料到的发现。我们的研究结果为NAc D1+细胞对自我启动的接近行为的特定贡献提供了新的证据,并将刺激D2+细胞如何促进学习的更新模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reward expectation and receipt differentially modulate the spiking of accumbens D1+ and D2+ neurons.

The nucleus accumbens (NAc) helps govern motivation to pursue reward. Two distinct sets of NAc projection neurons-expressing dopamine D1 vs. D2 receptors-are thought to promote and suppress motivated behaviors, respectively. However, support for this conceptual framework is limited: in particular, the spiking patterns of these distinct cell types during motivated behavior have been largely unknown. Using optogenetic tagging, we recorded the spiking of identified D1+ and D2+ neurons in the NAc core as unrestrained rats performed an operant task in which motivation to initiate work tracks recent reward rate. D1+ neurons preferentially increased firing as rats initiated trials and fired more when reward expectation was higher. By contrast, D2+ cells preferentially increased firing later in the trial, especially in response to reward delivery-a finding not anticipated from current theoretical models. Our results provide new evidence for the specific contribution of NAc D1+ cells to self-initiated approach behavior and will spur updated models of how D2+ cells contribute to learning.

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来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
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