Human hippocampal ripples align new experiences with a grid-like schema.

IF 15 1区 医学 Q1 NEUROSCIENCES
Zhibing Xiao, Xiongfei Wang, Jinbo Zhang, Jianxin Ou, Li He, Yukun Qu, Xiangyu Hu, Timothy E J Behrens, Yunzhe Liu
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引用次数: 0

Abstract

Humans form cognitive maps that enable inferences beyond direct experience, relying on hexagonal grid-cell-like neural codes as a schema for two-dimensional (2D) spaces. However, how new experiences align with this schema remains unknown. We recorded intracranial activity from 42 epilepsy patients while they learned rank relations among feature objects, then combined these features into compounds occupying a 2D conceptual space. Hippocampal ripples during brief pauses between learning trials increased with experience, signaling integration of the learned ranks. Crucially, ripple activity during post-learning rest predicted the later appearance of grid-like codes in the entorhinal and medial prefrontal cortex (mPFC) when participants inferred unseen relations among compounds. Ripples synchronized with mPFC during rest were specifically associated with later schema-based inference rather than direct memory retrieval. These findings show that hippocampal ripples align new experiences with an existing grid-like schema, transforming discrete events into structured knowledge that supports flexible reasoning in human cognition.

人类的海马体波纹将新的体验与网格状的图式联系起来。
人类依靠六边形网格细胞般的神经编码作为二维空间的图式,形成认知地图,使推理超越直接经验。然而,新体验如何与这种模式相一致仍然未知。我们记录了42名癫痫患者在学习特征对象之间的等级关系时的颅内活动,然后将这些特征组合成占据二维概念空间的化合物。在学习试验之间的短暂停顿期间,海马体的涟漪随着经验的增加而增加,这表明学习队伍的整合。至关重要的是,学习后休息期间的涟漪活动预测了当参与者推断化合物之间看不见的关系时,内嗅和内侧前额叶皮层(mPFC)中网格状代码的后期出现。休息时与mPFC同步的涟漪与后来的基于图式的推理而不是直接记忆检索有关。这些发现表明,海马体波纹将新的体验与现有的网格状图式结合起来,将离散的事件转化为结构化的知识,支持人类认知中的灵活推理。
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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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