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性别和阿尔茨海默病的5xFAD模型对进食时间的睡眠及空间学习反应的影响。

The impacts of sex and the 5xFAD model of Alzheimer's disease on the sleep and spatial learning responses to feeding time.

作者信息

Campbell Katrina J, Jiang Peng, Olker Christopher, Lin Xuanyi, Kim Sarah Y, Lee Christopher J, Song Eun Joo, Turek Fred W, Vitaterna Martha Hotz

机构信息

Center for Sleep and Circadian Biology, Northwestern University, Evanston, IL, United States.

Department of Neurobiology, Weinberg College of Arts and Sciences, Northwestern University, Evanston, IL, United States.

出版信息

Front Neurol. 2024 Jul 31;15:1430989. doi: 10.3389/fneur.2024.1430989. eCollection 2024.

DOI:10.3389/fneur.2024.1430989
PMID:39144714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11322461/
Abstract

INTRODUCTION

The relationships between the feeding rhythm, sleep and cognition in Alzheimer's disease (AD) are incompletely understood, but meal time could provide an easy-to-implement method of curtailing disease-associated disruptions in sleep and cognition. Furthermore, known sex differences in AD incidence could relate to sex differences in circadian rhythm/sleep/cognition interactions.

METHODS

The 5xFAD transgenic mouse model of AD and non-transgenic wild-type controls were studied. Both female and male mice were used. Food access was restricted each day to either the 12-h light phase (light-fed groups) or the 12-h dark phase (dark-fed groups). Sleep (electroencephalographic/electromyographic) recording and cognitive behavior measures were collected.

RESULTS

The 5xFAD genotype reduces NREM and REM as well as the number of sleep spindles. In wild-type mice, light-fed groups had disrupted vigilance state amounts, characteristics, and rhythms relative to dark-fed groups. These feeding time differences were reduced in 5xFAD mice. Sex modulates these effects. 5xFAD mice display poorer spatial memory that, in female mice, is curtailed by dark phase feeding. Similarly, female 5xFAD mice have decreased anxiety-associated behavior. These emotional and cognitive measures are correlated with REM amount.

DISCUSSION

Our study demonstrates that the timing of feeding can alter many aspects of wake, NREM and REM. Unexpectedly, 5xFAD mice are less sensitive to these feeding time effects. 5xFAD mice demonstrate deficits in cognition which are correlated with REM, suggesting that this circadian-timed aspect of sleep may link feeding time and cognition. Sex plays an important role in regulating the impact of feeding time on sleep and cognition in both wild-type and 5xFAD mice, with females showing a greater cognitive response to feeding time than males.

摘要

引言

阿尔茨海默病(AD)中进食节奏、睡眠与认知之间的关系尚未完全明确,但进餐时间可能提供一种易于实施的方法,以减少与疾病相关的睡眠和认知紊乱。此外,已知AD发病率的性别差异可能与昼夜节律/睡眠/认知相互作用中的性别差异有关。

方法

研究了AD的5xFAD转基因小鼠模型和非转基因野生型对照。使用了雌性和雄性小鼠。每天将食物获取限制在12小时光照期(光照喂养组)或12小时黑暗期(黑暗喂养组)。收集睡眠(脑电图/肌电图)记录和认知行为测量数据。

结果

5xFAD基因型减少了非快速眼动睡眠(NREM)和快速眼动睡眠(REM)以及睡眠纺锤波的数量。在野生型小鼠中,光照喂养组相对于黑暗喂养组,其警觉状态的数量、特征和节律受到干扰。这些进食时间差异在5xFAD小鼠中有所减少。性别调节这些影响。5xFAD小鼠表现出较差的空间记忆,在雌性小鼠中,黑暗期喂养可减少这种情况。同样,雌性5xFAD小鼠的焦虑相关行为减少。这些情绪和认知测量结果与REM量相关。

讨论

我们的研究表明,进食时间可改变清醒、NREM和REM的许多方面。出乎意料的是,5xFAD小鼠对这些进食时间效应不太敏感。5xFAD小鼠表现出与REM相关的认知缺陷,这表明睡眠的这种昼夜定时方面可能将进食时间与认知联系起来。性别在调节进食时间对野生型和5xFAD小鼠睡眠和认知的影响方面起着重要作用,雌性比雄性对进食时间表现出更大的认知反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/600377fdbb47/fneur-15-1430989-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/da6f06c98439/fneur-15-1430989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/802ddf598c52/fneur-15-1430989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/364be4f8a509/fneur-15-1430989-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/b33c6de553b1/fneur-15-1430989-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/8c05a1d0aed5/fneur-15-1430989-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/eab24d617518/fneur-15-1430989-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/a150cb0f50c2/fneur-15-1430989-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/600377fdbb47/fneur-15-1430989-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/da6f06c98439/fneur-15-1430989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/802ddf598c52/fneur-15-1430989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/364be4f8a509/fneur-15-1430989-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/d3f579b85f42/fneur-15-1430989-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/b33c6de553b1/fneur-15-1430989-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/8c05a1d0aed5/fneur-15-1430989-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/eab24d617518/fneur-15-1430989-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/a150cb0f50c2/fneur-15-1430989-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6960/11322461/600377fdbb47/fneur-15-1430989-g009.jpg

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