Sleep, Sirtuin 1 and Alzheimer’s disease: A review

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2022-01-01 DOI:10.1016/j.nbas.2022.100050
Mehrane Mehramiz , Tenielle Porter , Simon M. Laws , Stephanie R. Rainey-Smith
{"title":"Sleep, Sirtuin 1 and Alzheimer’s disease: A review","authors":"Mehrane Mehramiz ,&nbsp;Tenielle Porter ,&nbsp;Simon M. Laws ,&nbsp;Stephanie R. Rainey-Smith","doi":"10.1016/j.nbas.2022.100050","DOIUrl":null,"url":null,"abstract":"<div><p>Sleep plays a major role in brain health, and cognition. Disrupted sleep is a well-described symptom of Alzheimer’s disease (AD). However, accumulating evidence suggests suboptimal sleep also increases AD risk. The deacetylase Sirtuin 1 (Sirt 1), encoded by the <em>SIRT1</em> gene, impacts sleep via its relationship to wake-sleep neurotransmitters and somnogens. Evidence from animal and human studies supports a significant and complex relationship between sleep, Sirt 1/ <em>SIRT1</em> and AD. Numerous hypotheses attempt to explain the critical impact of Sirt 1/ <em>SIRT1</em> on wake- and sleep- promoting neurons, their related mechanisms and neurotransmitters. However, there is a paucity of studies assessing the interaction between sleep and Sirt 1/ <em>SIRT1</em>, as a principal component of sleep regulation, on AD pathology. In this review, we explore the potential association between Sirt 1/ <em>SIRT1</em>, sleep, and AD aetiology. Given sleep is a likely modifiable risk factor for AD, and recent studies suggest Sirt 1/ <em>SIRT1</em> activation can be modulated by lifestyle or dietary approaches, further research in this area is required to explore its potential as a target for AD prevention and treatment.</p></div>","PeriodicalId":72131,"journal":{"name":"Aging brain","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4d/f6/main.PMC9997138.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aging brain","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589958922000226","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Sleep plays a major role in brain health, and cognition. Disrupted sleep is a well-described symptom of Alzheimer’s disease (AD). However, accumulating evidence suggests suboptimal sleep also increases AD risk. The deacetylase Sirtuin 1 (Sirt 1), encoded by the SIRT1 gene, impacts sleep via its relationship to wake-sleep neurotransmitters and somnogens. Evidence from animal and human studies supports a significant and complex relationship between sleep, Sirt 1/ SIRT1 and AD. Numerous hypotheses attempt to explain the critical impact of Sirt 1/ SIRT1 on wake- and sleep- promoting neurons, their related mechanisms and neurotransmitters. However, there is a paucity of studies assessing the interaction between sleep and Sirt 1/ SIRT1, as a principal component of sleep regulation, on AD pathology. In this review, we explore the potential association between Sirt 1/ SIRT1, sleep, and AD aetiology. Given sleep is a likely modifiable risk factor for AD, and recent studies suggest Sirt 1/ SIRT1 activation can be modulated by lifestyle or dietary approaches, further research in this area is required to explore its potential as a target for AD prevention and treatment.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
睡眠、Sirtuin 1与阿尔茨海默病:综述
睡眠在大脑健康和认知方面起着重要作用。睡眠中断是阿尔茨海默病(AD)的一个很好的症状。然而,越来越多的证据表明,次优睡眠也会增加阿尔茨海默病的风险。由SIRT1基因编码的去乙酰化酶Sirtuin 1 (SIRT1)通过其与清醒-睡眠神经递质和睡眠激素的关系影响睡眠。来自动物和人类研究的证据表明,睡眠、SIRT1 / SIRT1和AD之间存在重要而复杂的关系。许多假说试图解释SIRT1 / SIRT1对促进觉醒和睡眠的神经元及其相关机制和神经递质的关键影响。然而,缺乏研究评估睡眠与SIRT1 / SIRT1之间的相互作用,SIRT1作为睡眠调节的主要组成部分,对AD病理的影响。在这篇综述中,我们探讨了SIRT1 / SIRT1、睡眠和AD病因之间的潜在关联。鉴于睡眠可能是阿尔茨海默病的一个可改变的危险因素,并且最近的研究表明SIRT1 / SIRT1激活可以通过生活方式或饮食方式调节,因此需要在该领域进一步研究以探索其作为阿尔茨海默病预防和治疗目标的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
自引率
0.00%
发文量
0
期刊最新文献
Age-related differences in structural and resting-state functional brain network organization across the adult lifespan: A cross-sectional study Age-related fornix decline predicts conservative response strategy-based slowing in perceptual decision-making Age-related decline in social interaction is associated with decreased c-Fos induction in select brain regions independent of oxytocin receptor expression profiles Innate immunity in brain aging and neurodegeneration Neural correlates of home-based intervention effects on value-based sequential decision-making in healthy older adults
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1