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Sleep fMRI with simultaneous electrophysiology at 9.4 T in male mice

Sleep is ubiquitous and essential, but its mechanisms remain unclear. Studies in animals and humans have provided insights of sleep at vastly different spatiotemporal scales. However, challenges remain to integrate local and global information of sleep. Therefore, we developed sleep fMRI based on si...

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Detalles Bibliográficos
Autores principales: Yu, Yalin, Qiu, Yue, Li, Gen, Zhang, Kaiwei, Bo, Binshi, Pei, Mengchao, Ye, Jingjing, Thompson, Garth J., Cang, Jing, Fang, Fang, Feng, Yanqiu, Duan, Xiaojie, Tong, Chuanjun, Liang, Zhifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039056/
https://www.ncbi.nlm.nih.gov/pubmed/36964161
http://dx.doi.org/10.1038/s41467-023-37352-9
Descripción
Sumario:Sleep is ubiquitous and essential, but its mechanisms remain unclear. Studies in animals and humans have provided insights of sleep at vastly different spatiotemporal scales. However, challenges remain to integrate local and global information of sleep. Therefore, we developed sleep fMRI based on simultaneous electrophysiology at 9.4 T in male mice. Optimized un-anesthetized mouse fMRI setup allowed manifestation of NREM and REM sleep, and a large sleep fMRI dataset was collected and openly accessible. State dependent global patterns were revealed, and state transitions were found to be global, asymmetrical and sequential, which can be predicted up to 17.8 s using LSTM models. Importantly, sleep fMRI with hippocampal recording revealed potentiated sharp-wave ripple triggered global patterns during NREM than awake state, potentially attributable to co-occurrence of spindle events. To conclude, we established mouse sleep fMRI with simultaneous electrophysiology, and demonstrated its capability by revealing global dynamics of state transitions and neural events.