工作记忆维持过程中的持续活动可预测人类海马体的长期记忆形成。

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-10-10 DOI:10.1016/j.neuron.2024.09.013
Jonathan Daume, Jan Kamiński, Yousef Salimpour, Andrea Gómez Palacio Schjetnan, William S Anderson, Taufik A Valiante, Adam N Mamelak, Ueli Rutishauser
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引用次数: 0

摘要

工作记忆(WM)和长期记忆(LTM)通常被视为独立的认知系统。人们对这两个系统在形成记忆时如何相互作用知之甚少。我们记录了人类内侧颞叶的单个神经元,当时患者在工作记忆中保留了新项目,并在随后完成了对相同项目的识别记忆测试。在海马体而非杏仁核中,WM内容选择性持续活动的水平可预测该项目后来是被高置信度识别还是被遗忘。相比之下,同一细胞中的视觉诱发活动并不能预测LTM的形成。在LTM检索过程中,记忆选择性神经元会对在WM中保持高持续活动的熟悉刺激做出更强烈的反应。我们的研究表明,海马中相同细胞的持续活动同时支持WM维持和LTM编码,从而揭示了这两种记忆系统中共同的单神经元成分。
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Persistent activity during working memory maintenance predicts long-term memory formation in the human hippocampus.

Working memory (WM) and long-term memory (LTM) are often viewed as separate cognitive systems. Little is known about how these systems interact when forming memories. We recorded single neurons in the human medial temporal lobe while patients maintained novel items in WM and completed a subsequent recognition memory test for the same items. In the hippocampus, but not in the amygdala, the level of WM content-selective persistent activity during WM maintenance was predictive of whether the item was later recognized with high confidence or forgotten. By contrast, visually evoked activity in the same cells was not predictive of LTM formation. During LTM retrieval, memory-selective neurons responded more strongly to familiar stimuli for which persistent activity was high while they were maintained in WM. Our study suggests that hippocampal persistent activity of the same cells supports both WM maintenance and LTM encoding, thereby revealing a common single-neuron component of these two memory systems.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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