Topography of putative bi-directional interaction between hippocampal sharp-wave ripples and neocortical slow oscillations.

IF 15 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2025-03-05 Epub Date: 2025-01-27 DOI:10.1016/j.neuron.2024.12.019
Rachel A Swanson, Elisa Chinigò, Daniel Levenstein, Mihály Vöröslakos, Navid Mousavi, Xiao-Jing Wang, Jayeeta Basu, György Buzsáki
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Abstract

Systems consolidation relies on coordination between hippocampal sharp-wave ripples (SWRs) and neocortical UP/DOWN states during sleep. However, whether this coupling exists across the neocortex and the mechanisms enabling it remains unknown. By combining electrophysiology in mouse hippocampus (HPC) and retrosplenial cortex (RSC) with wide-field imaging of the dorsal neocortex, we found spatially and temporally precise bi-directional hippocampo-neocortical interaction. HPC multi-unit activity and SWR probability were correlated with UP/DOWN states in the default mode network (DMN), with the highest modulation by the RSC in deep sleep. Further, some SWRs were preceded by the high rebound excitation accompanying DMN DOWN → UP transitions, whereas large-amplitude SWRs were often followed by DOWN states originating in the RSC. We explain these electrophysiological results with a model in which the HPC and RSC are weakly coupled excitable systems capable of bi-directional perturbation and suggest that the RSC may act as a gateway through which SWRs can perturb downstream cortical regions via cortico-cortical propagation of DOWN states.

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海马体急波波纹和新皮层慢波之间假定的双向相互作用的地形。
系统巩固依赖于睡眠期间海马锐波波纹(SWRs)和新皮层上下状态之间的协调。然而,这种耦合是否存在于新皮层以及其机制仍然未知。通过将小鼠海马(HPC)和脾后皮层(RSC)电生理与背侧新皮层的宽视场成像相结合,我们发现了空间和时间上精确的双向海马-新皮层相互作用。HPC多单元活动和SWR概率与默认模式网络(DMN)的UP/DOWN状态相关,其中深度睡眠时RSC的调制作用最大。此外,在一些swr发生之前,伴随着DMN DOWN→UP转变的高反弹激励,而在大振幅swr之后,通常伴随着起源于RSC的DOWN状态。我们用一个模型来解释这些电生理结果,在这个模型中,HPC和RSC是能够双向扰动的弱耦合可兴奋系统,并表明RSC可能作为swr通过皮质-皮质传播DOWN状态来扰动下游皮层区域的门户。
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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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