Sleep and vigilance states: Embracing spatiotemporal dynamics.

Neuron

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address:

Published: July 2023

AI Article Synopsis

  • The traditional view of sleep and wakefulness is that these states are stable and driven by specific brain interactions, but new research shows they are actually dynamic and vary by region.
  • Recent findings indicate that sleep-like and wake-like states can occur simultaneously in different parts of the brain and that there are rapid changes during transitions between these states.
  • This evolving perspective emphasizes the need for more nuanced approaches to studying and enhancing sleep, suggesting that understanding the complexity of brain activity could lead to better sleep interventions.

Article Abstract

The classic view of sleep and vigilance states is a global stationary perspective driven by the interaction between neuromodulators and thalamocortical systems. However, recent data are challenging this view by demonstrating that vigilance states are highly dynamic and regionally complex. Spatially, sleep- and wake-like states often co-occur across distinct brain regions, as in unihemispheric sleep, local sleep in wakefulness, and during development. Temporally, dynamic switching prevails around state transitions, during extended wakefulness, and in fragmented sleep. This knowledge, together with methods monitoring brain activity across multiple regions simultaneously at millisecond resolution with cell-type specificity, is rapidly shifting how we consider vigilance states. A new perspective incorporating multiple spatial and temporal scales may have important implications for considering the governing neuromodulatory mechanisms, the functional roles of vigilance states, and their behavioral manifestations. A modular and dynamic view highlights novel avenues for finer spatiotemporal interventions to improve sleep function.

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Source
http://dx.doi.org/10.1016/j.neuron.2023.04.012DOI Listing

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