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. 2023 Aug;27(4):1495-1504.
doi: 10.1007/s11325-022-02719-7. Epub 2022 Oct 7.

NREM sleep loss increases neurofilament light chain levels in APP/PS1 and C57BL/6 J mice

Shunjie Liu  1 , Zhiying Zhang  1 , Shuangming Shi  1 , Yangyang Meng  1 , Xiaofeng Zhang  1 , Qingfeng Lei  1 , Zhong Li  2   3   4
Affiliations

NREM sleep loss increases neurofilament light chain levels in APP/PS1 and C57BL/6 J mice

Shunjie Liu et al. Sleep Breath. 2023 Aug.

Abstract

Purpose: Sleep disturbances exacerbate the progression of Alzheimer's disease (AD), but disturbances of non-rapid eye movement (NREM) sleep and rapid eye movement (REM) sleep may have different effects. Neurofilament light chain (NfL), an axon-specific protein, is an indicator of the severity of neuronal apoptosis. To investigate whether or not NREM or REM sleep is crucial to neuronal survival, we examined the effects of induced NREM or REM sleep loss on NfL levels in APP/PS1 mice, a model of AD, and their wild-type (WT) C57BL/6 J littermates.

Methods: At 6 months of age, WT mice and AD mice were equally divided into six groups, namely, the WT-normal sleep (S), WT-total sleep deprivation (TSD), WT-REM deprivation (RD), AD-S, AD-TSD and AD-RD groups, according to the type of sleep intervention applied. All mice underwent 6 days of sleep intervention. Cerebrospinal fluid (CSF) and plasma NfL levels were measured at baseline and on days 2, 4 and 6, and spatial memory was assessed in the Morris water maze (MWM) test.

Results: Among the 18 WT and 18 AD mice, CSF and plasma NfL levels were higher in AD-TSD mice than in AD-S or AD-RD mice, while no significant difference was observed between the latter two groups. In AD-TSD mice, CSF and plasma NfL levels increased with the duration of sleep deprivation. A similar pattern of results was observed for the WT groups.

Conclusions: NREM sleep loss may increase CSF and plasma NfL levels in both WT and AD mice.

Keywords: APP/PS1 mice; C57BL/6 J mice; Neurofilament light chain; Non-rapid eye movement sleep; Sleep deprivation.

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