跨越尺度:综合光磁成像显示的单神经元招募和慢波事件的连续皮层传播。

IF 4.5 2区 医学 Q1 NEUROIMAGING
Dirk Cleppien, Miriam Schwalm, Hendrik Backhaus, Ting Fu, Felipe Aedo-Jury, Gaby Schneider, Albrecht Stroh
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引用次数: 0

摘要

种群上升状态或慢波事件(SWEs)是哺乳动物大脑皮层慢波状态的主要特征,发生在深度睡眠或某些麻醉状态下。我们利用光学和翻译相关功能磁共振成像(fMRI),在从单个神经元到整个皮层的观察尺度上探索了SWE的神经元募集和繁殖。通过对小鼠视觉皮层的双光子钙成像,我们发现观察到的局部微网络的所有活跃细胞都参与了群体宽慢波。实现光磁集成概念,包括在大鼠中同时使用快速皮质线扫描功能磁共振成像进行纤维光度测定,我们识别并跟踪在皮质中传播的SWE。通过非侵入性线扫描功能磁共振成像,我们可以证明慢波事件的连续皮层传播。这为监测神经生理学定义的信号(这里是SWE)的时空动态打开了大门。对慢波事件传播的非侵入性监测可能代表啮齿动物和人类局部和全局皮质网络功能完整性的代理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crossing the scales: single-neuron recruitment and continuous cortical propagation of slow wave events revealed by integrative opto-magnetic imaging.

Population up states or slow wave events (SWEs) represent the main feature of slow wave brain state in mammalian cortex, occurring during deep sleep or under certain types of anesthesia. We explore the neuronal recruitment and propagation of SWE on observational scales ranging from single neurons to the entire cortex, intertwining optical and translationally relevant functional MRI (fMRI). By two-photon calcium imaging in mouse visual cortex, we demonstrate that all active cells of the observed local micro network participate in a population wide slow wave. Implementing an optomagnetic-integration concept, involving simultaneous fiber photometry with fast cortical line-scanning fMRI in rats, we identify and follow propagating SWE across the cortex. We can demonstrate continuous cortical propagation of a slow wave event, by non-invasive line-scanning fMRI. This opens the door for monitoring the spatiotemporal dynamics of a neurophysiological-defined signal - here SWE. Non-invasive monitoring of slow wave event propagation might represent a proxy for the functional integrity of local and global cortical networks in rodents and humans.

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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
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