Time-dependent effects of high-fat diet on cognition and cerebral insulin signaling: Window for recovery and potential therapeutic target

IF 5.3 3区 医学 Q2 CELL BIOLOGY
Tianchuang Zhao , Qi Li , Xiaodan Wang , Bo Tang , Xueming Zhang , Hao Yu , Ziyi Li
{"title":"Time-dependent effects of high-fat diet on cognition and cerebral insulin signaling: Window for recovery and potential therapeutic target","authors":"Tianchuang Zhao ,&nbsp;Qi Li ,&nbsp;Xiaodan Wang ,&nbsp;Bo Tang ,&nbsp;Xueming Zhang ,&nbsp;Hao Yu ,&nbsp;Ziyi Li","doi":"10.1016/j.mad.2024.111955","DOIUrl":null,"url":null,"abstract":"<div><p>While high-fat diet (HFD)-induced obesity is a major threat to global public health, the effect of HFD on cognition and insulin signaling during ageing remains controversial. The aim of this study was to characterize the dynamic alterations in cognition and cerebral insulin signaling during 6-month HFD consumption, and to investigate the potential therapeutic target and optimal timing to rescue obesity-related cognitive deficits. In the present study, impaired memory retention induced by 2-month HFD was recovered after 4 months on HFD. Prolonged (6-month) HFD did not further enhance tau hyperphosphorylation and β-amyloid deposition, which was consistent with the alleviation of memory retention. In brain insulin signaling, 2-month HFD increased IRS-1 and p-IRS-1(Ser307)/IRS-1, while decreasing pAKT(Ser473)/AKT, PI3K and mTOR; 4-month HFD decreased IRS-1 and pAKT(Ser473)/AKT, while increasing AKT; 6-month HFD increased IRS-1, pAKT(Ser473)/AKT, and mTOR, while decreasing p-IRS-1(Ser307)/IRS-1, PI3K and AKT. Notably, bioinformatic analysis revealed a rhythmic process presented only in 4-month HFD group, with <em>Srebf1</em> emerging as a link between circadian rhythms and insulin signaling pathway. These results suggest that prolonged HFD prevents further cognitive decline and the progression of Alzheimer’s disease (AD)-related pathologies during ageing. Moreover, there may be a window for recovery, in which <em>Srebf1</em> acts as a self-recovery switch to address obesity-related cognitive disorders in elders.</p></div>","PeriodicalId":18340,"journal":{"name":"Mechanisms of Ageing and Development","volume":"220 ","pages":"Article 111955"},"PeriodicalIF":5.3000,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mechanisms of Ageing and Development","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0047637424000551","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

While high-fat diet (HFD)-induced obesity is a major threat to global public health, the effect of HFD on cognition and insulin signaling during ageing remains controversial. The aim of this study was to characterize the dynamic alterations in cognition and cerebral insulin signaling during 6-month HFD consumption, and to investigate the potential therapeutic target and optimal timing to rescue obesity-related cognitive deficits. In the present study, impaired memory retention induced by 2-month HFD was recovered after 4 months on HFD. Prolonged (6-month) HFD did not further enhance tau hyperphosphorylation and β-amyloid deposition, which was consistent with the alleviation of memory retention. In brain insulin signaling, 2-month HFD increased IRS-1 and p-IRS-1(Ser307)/IRS-1, while decreasing pAKT(Ser473)/AKT, PI3K and mTOR; 4-month HFD decreased IRS-1 and pAKT(Ser473)/AKT, while increasing AKT; 6-month HFD increased IRS-1, pAKT(Ser473)/AKT, and mTOR, while decreasing p-IRS-1(Ser307)/IRS-1, PI3K and AKT. Notably, bioinformatic analysis revealed a rhythmic process presented only in 4-month HFD group, with Srebf1 emerging as a link between circadian rhythms and insulin signaling pathway. These results suggest that prolonged HFD prevents further cognitive decline and the progression of Alzheimer’s disease (AD)-related pathologies during ageing. Moreover, there may be a window for recovery, in which Srebf1 acts as a self-recovery switch to address obesity-related cognitive disorders in elders.

Abstract Image

高脂饮食对认知和脑胰岛素信号转导的时间依赖性影响:恢复窗口和潜在治疗目标。
高脂饮食(HFD)诱发的肥胖症是全球公共健康的主要威胁,但高脂饮食对认知能力和衰老过程中胰岛素信号传导的影响仍存在争议。本研究的目的是描述食用6个月HFD期间认知和脑胰岛素信号传导的动态变化,并探讨挽救肥胖相关认知缺陷的潜在治疗目标和最佳时机。在本研究中,2个月高脂饮食引起的记忆保持受损在高脂饮食4个月后得到恢复。长期(6 个月)高脂饮食并没有进一步增强 tau 过度磷酸化和 β 淀粉样蛋白沉积,这与记忆保持的缓解是一致的。在脑胰岛素信号转导方面,2个月的高频分解胰岛素增加了IRS-1和p-IRS-1(Ser307)/IRS-1,同时降低了pAKT(Ser473)/AKT、PI3K和mTOR;4个月的高频分解减少了IRS-1和pAKT(Ser473)/AKT,同时增加了AKT;6个月的高频分解增加了IRS-1、pAKT(Ser473)/AKT和mTOR,同时减少了p-IRS-1(Ser307)/IRS-1、PI3K和AKT。值得注意的是,生物信息学分析表明,只有为期4个月的高频分解组才出现节律过程,Srebf1成为昼夜节律和胰岛素信号通路之间的纽带。这些结果表明,在老龄化过程中,长期高频分解膳食可防止认知能力进一步下降和阿尔茨海默病(AD)相关病变的进展。此外,Srebf1可能存在一个恢复窗口,在这个窗口中,Srebf1可作为自我恢复开关,解决老年人与肥胖相关的认知障碍问题。
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 求助全文
来源期刊
CiteScore
11.10
自引率
1.90%
发文量
79
审稿时长
32 days
期刊介绍: Mechanisms of Ageing and Development is a multidisciplinary journal aimed at revealing the molecular, biochemical and biological mechanisms that underlie the processes of aging and development in various species as well as of age-associated diseases. Emphasis is placed on investigations that delineate the contribution of macromolecular damage and cytotoxicity, genetic programs, epigenetics and genetic instability, mitochondrial function, alterations of metabolism and innovative anti-aging approaches. For all of the mentioned studies it is necessary to address the underlying mechanisms. Mechanisms of Ageing and Development publishes original research, review and mini-review articles. The journal also publishes Special Issues that focus on emerging research areas. Special issues may include all types of articles following peered review. Proposals should be sent directly to the Editor-in-Chief.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信