» Articles » PMID: 37600754

Sleep Deprivation Aggravated Amyloid β Oligomers-induced Damage to the Cerebellum of Rats: Evidence from Magnetic Resonance Imaging

Overview
Journal Aging Brain
Publisher Elsevier
Specialty Geriatrics
Date 2023 Aug 21
PMID 37600754
Authors
Affiliations
Soon will be listed here.
Abstract

For quite a long time, researches on Alzheimer's disease (AD) primarily focused on the cortex and hippocampus, while the cerebellum has been ignored because of its abnormalities considered to appear in the late stage of AD. In recent years, increasing evidence suggest that the cerebellar pathological changes possibly occur in the preclinical phase of AD, which is also associated with sleep disorder. Sleep disturbance is a high risk factor of AD. However, the changes and roles of cerebellum has rarely been reported under conditions of AD accompanied with sleep disorders. In this study, using an amyloid-β oligomers (AβO)-induced rat model of AD subjected to sleep deprivation, combining with a 7.0 T animals structural magnetic resonance imaging (MRI), we assessed structural changes of cerebellum in MRI. Our results showed that sleep deprivation combined with AβO led to an increased FA value in the anterior lobe of cerebellum, decreased ADC value in the cerebellar lobes and cerebellar nuclei, and increased cerebellum volume. Besides that, sleep deprivation exacerbated the damage of AβO to the cerebellar structural network. This study demonstrated that sleep deprivation could aggravate the damage to cerebellum induced by AβO. The present findings provide supporting evidence for the involvement of cerebellum in the early pathology of AD and sleep loss. Our data would contribute to advancing the understanding of the mysterious role of cerebellum in AD and sleep disorders, as well as would be helpful for developing non-invasive MRI biomarkers for screening early AD patients with self-reported sleep disturbances.

References
1.
Toniolo S, Serra L, Olivito G, Marra C, Bozzali M, Cercignani M . Patterns of Cerebellar Gray Matter Atrophy Across Alzheimer's Disease Progression. Front Cell Neurosci. 2018; 12:430. PMC: 6255820. DOI: 10.3389/fncel.2018.00430. View

2.
Reiman E, Quiroz Y, Fleisher A, Chen K, Velez-Pardo C, Jimenez-Del-Rio M . Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study. Lancet Neurol. 2012; 11(12):1048-56. PMC: 4181671. DOI: 10.1016/S1474-4422(12)70228-4. View

3.
Xu W, De Carvalho F, Clarke A, Jackson A . Communication from the cerebellum to the neocortex during sleep spindles. Prog Neurobiol. 2020; 199:101940. PMC: 7938225. DOI: 10.1016/j.pneurobio.2020.101940. View

4.
Sotak C . Nuclear magnetic resonance (NMR) measurement of the apparent diffusion coefficient (ADC) of tissue water and its relationship to cell volume changes in pathological states. Neurochem Int. 2004; 45(4):569-82. DOI: 10.1016/j.neuint.2003.11.010. View

5.
Ashburner J, Friston K . Voxel-based morphometry--the methods. Neuroimage. 2000; 11(6 Pt 1):805-21. DOI: 10.1006/nimg.2000.0582. View