• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

衰老作为阿尔茨海默病预防和治疗的靶点。

Aging as a target for the prevention and treatment of Alzheimer's disease.

作者信息

Yap Lauren E, Hunt James E, Turner Raymond Scott

机构信息

Department of Neurology, Memory Disorders Program, Georgetown University, Washington, DC, United States.

出版信息

Front Neurol. 2024 Apr 5;15:1376104. doi: 10.3389/fneur.2024.1376104. eCollection 2024.

DOI:10.3389/fneur.2024.1376104
PMID:38645748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11027067/
Abstract

Alzheimer's disease (AD), the most common etiology of dementia in older adults, is projected to double in prevalence over the next few decades. Current treatments for AD manage symptoms or slow progressive decline, but are accompanied by significant inconvenience, risk, and cost. Thus, a better understanding of the risk factors and pathophysiology of AD is needed to develop novel prevention and treatment strategies. Aging is the most important risk factor for AD. Elucidating molecular mechanisms of aging may suggest novel therapeutic targets. While aging is inevitable, it may be accelerated by caloric excess and slowed by caloric restriction (CR) or intermittent fasting. As such, CR may slow aging and reduce the risk of all diseases of aging, including dementia due to AD. The literature on CR, intermittent fasting, and treatment with polyphenols such as resveratrol-a pharmacologic CR-mimetic-supports this hypothesis based on clinical outcomes as well as biomarkers of aging and AD. More studies exploring the role of CR in regulating aging and AD progression in man are needed to fill gaps in our understanding and develop safer and more effective strategies for the prevention and treatment of AD.

摘要

阿尔茨海默病(AD)是老年人痴呆最常见的病因,预计在未来几十年患病率将翻倍。目前治疗AD的方法是控制症状或减缓病情进展,但会带来极大不便、风险和成本。因此,需要更好地了解AD的危险因素和病理生理学,以制定新的预防和治疗策略。衰老 是AD最重要的危险因素。阐明衰老的分子机制可能会提示新的治疗靶点。虽然衰老是不可避免的,但热量过剩可能会加速衰老,而热量限制(CR)或间歇性禁食可能会减缓衰老。因此,CR可能会减缓衰老并降低所有衰老相关疾病的风险,包括AD所致痴呆。关于CR、间歇性禁食以及使用白藜芦醇等多酚类物质(一种模拟CR的药物)进行治疗的文献,基于临床结果以及衰老和AD的生物标志物,支持了这一假设。需要更多研究来探索CR在调节人类衰老和AD进展中的作用,以填补我们认知上的空白,并制定更安全、更有效的AD预防和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0103/11027067/5fe96844c500/fneur-15-1376104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0103/11027067/5fe96844c500/fneur-15-1376104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0103/11027067/5fe96844c500/fneur-15-1376104-g001.jpg

相似文献

1
Aging as a target for the prevention and treatment of Alzheimer's disease.衰老作为阿尔茨海默病预防和治疗的靶点。
Front Neurol. 2024 Apr 5;15:1376104. doi: 10.3389/fneur.2024.1376104. eCollection 2024.
2
Intermittent fasting and caloric restriction ameliorate age-related behavioral deficits in the triple-transgenic mouse model of Alzheimer's disease.间歇性禁食和热量限制可改善阿尔茨海默病三联转基因小鼠模型中与年龄相关的行为缺陷。
Neurobiol Dis. 2007 Apr;26(1):212-20. doi: 10.1016/j.nbd.2006.12.019. Epub 2007 Jan 13.
3
NIA-AA Research Framework: Toward a biological definition of Alzheimer's disease.NIA-AA 研究框架:迈向阿尔茨海默病的生物学定义。
Alzheimers Dement. 2018 Apr;14(4):535-562. doi: 10.1016/j.jalz.2018.02.018.
4
Lifestyle Modifications and Nutritional Interventions in Aging-Associated Cognitive Decline and Alzheimer's Disease.衰老相关认知衰退和阿尔茨海默病中的生活方式改变与营养干预
Front Aging Neurosci. 2020 Jan 10;11:369. doi: 10.3389/fnagi.2019.00369. eCollection 2019.
5
Cognitive Reserve Relates to Functional Network Efficiency in Alzheimer's Disease.认知储备与阿尔茨海默病中的功能网络效率相关。
Front Aging Neurosci. 2018 Aug 21;10:255. doi: 10.3389/fnagi.2018.00255. eCollection 2018.
6
Caloric restriction: beneficial effects on brain aging and Alzheimer's disease.热量限制:对大脑衰老和阿尔茨海默病的有益影响。
Mamm Genome. 2016 Aug;27(7-8):300-19. doi: 10.1007/s00335-016-9647-6. Epub 2016 May 30.
7
Effects of intermittent fasting on cognitive health and Alzheimer's disease.间歇性禁食对认知健康和阿尔茨海默病的影响。
Nutr Rev. 2023 Aug 10;81(9):1225-1233. doi: 10.1093/nutrit/nuad021.
8
Clinical Insights on Caloric Restriction Mimetics for Mitigating Brain Aging and Related Neurodegeneration.热量限制模拟物在缓解大脑衰老和相关神经退行性变方面的临床见解。
Cell Mol Neurobiol. 2024 Oct 16;44(1):67. doi: 10.1007/s10571-024-01493-2.
9
Understanding the role of psychiatrists in the diagnosis and management of mild cognitive impairment and mild Alzheimer's disease dementia: a cross-sectional survey.理解精神科医生在轻度认知障碍和轻度阿尔茨海默病痴呆症的诊断和管理中的作用:一项横断面调查。
BMC Psychiatry. 2023 Oct 4;23(1):716. doi: 10.1186/s12888-023-05129-5.
10
Next Generation Therapeutic Strategy for Treatment and Prevention of Alzheimer's Disease and Aging-Associated Cognitive Decline: Transient, Once-in-a-Lifetime-Only Depletion of Intraneuronal Aβ (Aβ) by Its Targeted Degradation via Augmentation of Intra-Aβ-Cleaving Activities of BACE1 and/or BACE2.用于治疗和预防阿尔茨海默病和与衰老相关的认知能力下降的下一代治疗策略:通过增强 BACE1 和/或 BACE2 的 intra-Aβ 裂解活性,靶向性地使细胞内 Aβ (Aβ) 短暂、一次性耗尽。
Int J Mol Sci. 2023 Dec 18;24(24):17586. doi: 10.3390/ijms242417586.

引用本文的文献

1
Energy Metabolism and Brain Aging: Strategies to Delay Neuronal Degeneration.能量代谢与脑衰老:延缓神经元变性的策略
Cell Mol Neurobiol. 2025 Apr 21;45(1):38. doi: 10.1007/s10571-025-01555-z.
2
Natural Compounds for Preventing Age-Related Diseases and Cancers.天然化合物预防与年龄相关的疾病和癌症。
Int J Mol Sci. 2024 Jul 9;25(14):7530. doi: 10.3390/ijms25147530.
3
The features analysis of hemoglobin expression on visual information transmission pathway in early stage of Alzheimer's disease.阿尔茨海默病早期视觉信息传递通路中血红蛋白表达的特征分析。

本文引用的文献

1
Implication of the cooking oil-peroxidation product "hydroxynonenal" for Alzheimer's disease.食用油过氧化产物“羟基壬烯醛”与阿尔茨海默病的关联。
Front Aging Neurosci. 2023 Aug 25;15:1211141. doi: 10.3389/fnagi.2023.1211141. eCollection 2023.
2
Effect of long-term caloric restriction on DNA methylation measures of biological aging in healthy adults from the CALERIE trial.长期热量限制对 CALERIE 试验中健康成年人生物衰老的 DNA 甲基化测量的影响。
Nat Aging. 2023 Mar;3(3):248-257. doi: 10.1038/s43587-022-00357-y. Epub 2023 Feb 9.
3
2023 Alzheimer's disease facts and figures.
Sci Rep. 2024 Jul 8;14(1):15636. doi: 10.1038/s41598-024-64099-0.
2023 年阿尔茨海默病事实和数据。
Alzheimers Dement. 2023 Apr;19(4):1598-1695. doi: 10.1002/alz.13016. Epub 2023 Mar 14.
4
Obesity impacts the expression of Alzheimer's disease-related genes: The Framingham Heart Study.肥胖影响阿尔茨海默病相关基因的表达:弗雷明汉心脏研究。
Alzheimers Dement. 2023 Aug;19(8):3496-3505. doi: 10.1002/alz.12954. Epub 2023 Feb 22.
5
Hallmarks of aging: An expanding universe.衰老的特征:一个不断扩大的领域。
Cell. 2023 Jan 19;186(2):243-278. doi: 10.1016/j.cell.2022.11.001. Epub 2023 Jan 3.
6
Aging and aging-related diseases: from molecular mechanisms to interventions and treatments.衰老和与衰老相关的疾病:从分子机制到干预和治疗。
Signal Transduct Target Ther. 2022 Dec 16;7(1):391. doi: 10.1038/s41392-022-01251-0.
7
APOE4 impairs myelination via cholesterol dysregulation in oligodendrocytes.载脂蛋白 E4 通过调控少突胶质细胞胆固醇影响髓鞘形成。
Nature. 2022 Nov;611(7937):769-779. doi: 10.1038/s41586-022-05439-w. Epub 2022 Nov 16.
8
Twelve Months of Time-Restricted Feeding Improves Cognition and Alters Microbiome Composition Independent of Macronutrient Composition.限时进食 12 个月可改善认知功能,并改变微生物组组成,而与宏量营养素组成无关。
Nutrients. 2022 Sep 24;14(19):3977. doi: 10.3390/nu14193977.
9
High-fat diet-induced diabetes couples to Alzheimer's disease through inflammation-activated C/EBPβ/AEP pathway.高脂肪饮食诱导的糖尿病通过炎症激活的 C/EBPβ/AEP 通路与阿尔茨海默病相关。
Mol Psychiatry. 2022 Aug;27(8):3396-3409. doi: 10.1038/s41380-022-01600-z. Epub 2022 May 11.
10
Diabetes: Risk factor and translational therapeutic implications for Alzheimer's disease.糖尿病:阿尔茨海默病的风险因素和转化治疗意义。
Eur J Neurosci. 2022 Nov;56(9):5727-5757. doi: 10.1111/ejn.15619. Epub 2022 Feb 23.