Sleep deprivation aggravated amyloid β oligomers-induced damage to the cerebellum of rats: Evidence from magnetic resonance imaging

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2023-01-01 DOI:10.1016/j.nbas.2023.100091
Wensheng Guo , Xin Mao , Ding Han , Hongqi Wang , Wanning Zhang , Guitao Zhang , Ning Zhang , Binbin Nie , Hui Li , Yizhi Song , Yan Wu , Lirong Chang
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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.

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睡眠剥夺加重了β淀粉样蛋白寡聚物对大鼠小脑的损伤:来自磁共振成像的证据
长期以来,对阿尔茨海默病(AD)的研究主要集中在皮层和海马体,而小脑由于其异常被认为出现在AD晚期而被忽视。近年来,越来越多的证据表明,小脑病理变化可能发生在AD的临床前阶段,这也与睡眠障碍有关。睡眠障碍是AD的高危因素,但小脑在AD合并睡眠障碍的情况下的变化和作用很少报道。在本研究中,使用淀粉样蛋白-β寡聚物(AβO)诱导的睡眠剥夺AD大鼠模型,结合7.0T动物结构磁共振成像(MRI),我们在MRI中评估了小脑的结构变化。我们的研究结果表明,睡眠剥夺联合AβO导致小脑前叶的FA值增加,小脑叶和小脑核的ADC值降低,小脑体积增加。此外,睡眠剥夺加重了AβO对小脑结构网络的损伤。本研究表明,睡眠剥夺可加重AβO对小脑的损伤。目前的研究结果为小脑参与AD和睡眠丧失的早期病理提供了支持性证据。我们的数据将有助于加深对小脑在AD和睡眠障碍中神秘作用的理解,并有助于开发非侵入性MRI生物标志物,用于筛查自我报告睡眠障碍的早期AD患者。
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Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
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