El Kanbi, K. | bioRxiv Science

bioRxiv2023

EEG and computational aspects of how aging affects sleep slow waves

Sleep slow-waves have been reported to vary with age in human subjects, as well as in mouse, but the underlying mechanisms remain unclear. Here, we perform a precise quantification of the effect of aging on the shape and dynamics of sleep slow waves, in a large cohort of human subjects recorded with the electro-encephalogram (EEG) during sleep. The fine-structure analysis of slow waves reveals that they slow-down, increase of variability and decrease in amplitude with age. We next investigate a computational model of the genesis of slow-wave activity and model the aging by a global decrease of the strength of the external excitatory drive to the network. This simple model reproduces some of the main features observed in the EEG, suggesting that changes of long-range excitatory connection strength may explain the evolution of slow-waves with age.

neuroscience↗

bioRxiv2018

Improved sleep scoring in mice reveals human-like stages.

Rodents are the main animal model to study sleep. Yet, in spite of a large consensus on the distinction between rapid-eye-movements sleep (REM) and non-REM sleep (NREM) in both humans and rodent, there is still no equivalent in mice of the NREM subdivision classically described in humans.\n\nHere we propose a classification of sleep stages in mice, inspired by human sleep scoring. By using chronic recordings in medial prefrontal cortex (mPFC) and hippocampus we can classify three NREM stages with a stage N1 devoid of any low oscillatory activity and N3 with a high density of delta waves. These stages displayed the same evolution observed in human during the whole sleep or within sleep cycles. Importantly, as in human, N1 in mice is the first stage observed at sleep onset and is increased after sleep fragmentation in Orexin-/- mice, a mouse model of narcolepsy.\n\nWe also show that these substages are associated to massive modification of neuronal activity. Moreover, considering these stages allows to predict mPFC neurons evolution of firing rates across sleep period. Notably, neurons preferentially active within N3 decreased their activity over sleep while the opposite is seen for those preferentially active in N1 and N2.\n\nOverall this new approach shows the feasibility of NREM sleep sub-classification in rodents, and, in regard to the similarity between sleep in both species, will pave the way for further studies in sleep pathologies given the perturbation of specific sleep substages in human pathologies such as insomnia, somnambulism, night terrors, or fibromyalgia.

neuroscience↗