在空间记忆任务中,海马体-前额叶通讯子空间与行为和网络模式一致。

IF 2.7 3区 医学 Q3 NEUROSCIENCES
eNeuro Pub Date : 2025-09-25 Print Date: 2025-09-01 DOI:10.1523/ENEURO.0336-24.2025
Ryan A Young, Justin D Shin, Ziyi Guo, Shantanu P Jadhav
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引用次数: 0

摘要

有节奏的网络状态已被理论化,以促进大脑区域之间的交流,但这些振荡如何影响交流子空间,即调解区域间交流的低维神经活动模式,以及子空间如何影响行为尚不清楚。利用大鼠(雄性Long-Evans大鼠)的空间记忆任务,我们同时记录了海马CA1和前额皮质(PFC)的集合来解决这个问题。我们发现,任务行为与这些区域之间的低维共享子空间最一致,而不是在任何一个区域的局部活动。关键是,网络振荡和速度都会调制该通信子空间的结构和性能。为了理解通信空间,我们使用流形技术可视化了共享的CA1-PFC通信几何结构,并发现了环状结构。我们假设这些共享活动流形被用来调解任务行为。这些发现表明,记忆引导的行为是由CA1-PFC共同的相互作用驱动的,这种相互作用是由振荡状态动态调节的,为节律和行为相关的神经通讯之间的相互作用提供了一个新的视角。本研究揭示了在空间记忆任务中,海马体和前额叶皮层之间的共享通信子空间与行为模式和网络振荡是一致的。我们证明了这些共享子空间可以稳健地预测任务行为,而单独在任何一个区域的局部活动都不能。将这些任务子空间组织成不同的流形表明了区域间协调中的任务信息,这被认为是记忆引导行为的关键。此外,我们的研究结果强调了theta功率在调制这些通信动态中的重要性。这些见解为助记和行为过程背后的区域间神经机制提供了更深入的理解,这是神经科学界广泛感兴趣的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal-Prefrontal Communication Subspaces Align with Behavioral and Network Patterns in a Spatial Memory Task.

Rhythmic network states have been theorized to facilitate communication between brain regions, but how these oscillations influence communication subspaces, i.e., the low-dimensional neural activity patterns that mediate interregional communication, and in turn how subspaces impact behavior remain unclear. Using a spatial memory task in rats (male Long-Evans rats), we simultaneously recorded ensembles from hippocampal CA1 and the prefrontal cortex (PFC) to address this question. We found that task behaviors best aligned with low-dimensional, shared subspaces between these regions rather than local activity in either region. Critically, both network oscillations and speed modulated the structure and performance of this communication subspace. To understand the communication space, we visualized shared CA1-PFC communication geometry using manifold techniques and found ring-like structures. We hypothesize that these shared activity manifolds are utilized to mediate the task behavior. These findings suggest that memory-guided behaviors are driven by shared CA1-PFC interactions that are dynamically modulated by oscillatory states, offering a novel perspective on the interplay between rhythms and behaviorally relevant neural communication.

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来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
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