前瞻性偶然性解释了联想学习过程中的行为和多巴胺信号

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Lechen Qian, Mark Burrell, Jay A. Hennig, Sara Matias, Venkatesh N. Murthy, Samuel J. Gershman, Naoshige Uchida
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引用次数: 0

摘要

联想学习依赖于偶然性,即刺激预测结果的程度。尽管它很重要,但将偶然性与行为联系起来的神经机制仍然难以捉摸。在本研究中,我们检测了小鼠在巴甫洛夫偶然性退化任务中腹侧纹状体中多巴胺的活性——一个与联想学习有关的信号。我们发现,当额外奖励未被提示时,预期舔舐和多巴胺对条件刺激的反应都会下降,但如果有额外奖励提示,则保持不变。这些结果与使用传统权变定义或新的因果学习模型(ANCCR)的基于权变的解释相冲突,但可以通过配备适当的间隔状态表示的时间差异(TD)学习模型来解释。在TD框架内训练的递归神经网络开发的状态表示类似于我们最好的“手工制作”模型。我们的研究结果表明,TD误差可以作为描述偶然性和多巴胺能活性的一种测量方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prospective contingency explains behavior and dopamine signals during associative learning

Prospective contingency explains behavior and dopamine signals during associative learning

Associative learning depends on contingency, the degree to which a stimulus predicts an outcome. Despite its importance, the neural mechanisms linking contingency to behavior remain elusive. In the present study, we examined the dopamine activity in the ventral striatum—a signal implicated in associative learning—in a Pavlovian contingency degradation task in mice. We show that both anticipatory licking and dopamine responses to a conditioned stimulus decreased when additional rewards were delivered uncued, but remained unchanged if additional rewards were cued. These results conflict with contingency-based accounts using a traditional definition of contingency or a new causal learning model (ANCCR), but can be explained by temporal difference (TD) learning models equipped with an appropriate intertrial interval state representation. Recurrent neural networks trained within a TD framework develop state representations akin to our best ‘handcrafted’ model. Our findings suggest that the TD error can be a measure that describes both contingency and dopaminergic activity.

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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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