前额叶θ和β爆发之间的动态相互作用促进了灵活的学习。

IF 2.1 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Experimental Neurobiology Pub Date : 2025-12-31 Epub Date: 2025-11-06 DOI:10.5607/en25034
Hahyeon Park, Haseong Kim, Eunyoung Yeo, Alan Jung Park
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引用次数: 0

摘要

应对不断变化的环境的能力对健康的功能至关重要,然而这种灵活性在许多神经精神疾病中受到损害。然而,灵活行为背后的神经机制仍然难以捉摸。在这里,我们报告了内侧前额叶皮层(mPFC)的振荡动力学支持学习灵活地克服既定的行为偏见。小鼠执行了延迟的非匹配样本任务,尽管存在持续的手臂偏差,但仍需要逐个调整手臂选择策略。对延迟期局部场电位(LFPs)和单单元活动的解码分析揭示了小鼠在适应任务过程中不断进化的神经表征。值得注意的是,经θ (4~12 Hz)脉冲调制的mPFC神经元在获得新规则后选择性地编码了即将到来的选择信息。相比之下,β (12~30 Hz)爆发与持久性行为相关,似乎抑制了表现出适应性行为的小鼠的θ调节神经元放电。这些θ波和β波在延迟期间暂时分开,反映了一种动态门控机制。因此,β脉冲形成神经元集合体,由θ脉冲调节,以促进灵活的学习。这种动态的相互作用为认知灵活性提供了机制基础,并为精神分裂症和自闭症等神经精神疾病的认知僵化提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dynamic Interplay between Prefrontal Theta and Beta Bursts Facilitates Flexible Learning.

Dynamic Interplay between Prefrontal Theta and Beta Bursts Facilitates Flexible Learning.

Dynamic Interplay between Prefrontal Theta and Beta Bursts Facilitates Flexible Learning.

Dynamic Interplay between Prefrontal Theta and Beta Bursts Facilitates Flexible Learning.

The ability to cope with changing environments is critical for healthy functioning, yet this flexibility is impaired in many neuropsychiatric disorders. However, neural mechanisms underlying flexible behavior remain elusive. Here, we report that oscillatory dynamics in the medial prefrontal cortex (mPFC) support learning to flexibly overcome established behavioral bias. Mice performed a delayed non-match-to-sample task that required trial-by-trial adjustment of arm choice strategy despite persistent arm bias. Decoding analysis of delay-period local field potentials (LFPs) and single-unit activities revealed evolving neural representations across trials as mice adapted to the task. Notably, mPFC neurons modulated by theta (4~12 Hz) bursts selectively encoded upcoming choice information after acquiring the new rule. In contrast, beta (12~30 Hz) bursts correlated with perseverative behavior and appeared to inhibit theta-modulated neuronal firing in mice showing adaptive behavior. These theta and beta bursts were temporally separated over the delay period, reflecting a dynamic gating mechanism. Thus, beta bursts shape neuronal ensembles that are modulated by theta bursts to facilitate flexible learning. This dynamic interaction provides a mechanistic basis for cognitive flexibility and provides insights into cognitive rigidity seen in neuropsychiatric disorders such as schizophrenia and autism.

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来源期刊
Experimental Neurobiology
Experimental Neurobiology Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.30
自引率
4.20%
发文量
29
期刊介绍: Experimental Neurobiology is an international forum for interdisciplinary investigations of the nervous system. The journal aims to publish papers that present novel observations in all fields of neuroscience, encompassing cellular & molecular neuroscience, development/differentiation/plasticity, neurobiology of disease, systems/cognitive/behavioral neuroscience, drug development & industrial application, brain-machine interface, methodologies/tools, and clinical neuroscience. It should be of interest to a broad scientific audience working on the biochemical, molecular biological, cell biological, pharmacological, physiological, psychophysical, clinical, anatomical, cognitive, and biotechnological aspects of neuroscience. The journal publishes both original research articles and review articles. Experimental Neurobiology is an open access, peer-reviewed online journal. The journal is published jointly by The Korean Society for Brain and Neural Sciences & The Korean Society for Neurodegenerative Disease.
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