• 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

热量限制与细胞衰老。

Caloric restriction and cellular senescence.

机构信息

Charles Perkins Centre and Central Clinical School, The University of Sydney, Australia; Department of Medicine, Washington University School of Medicine, St. Louis, USA; Department of Clinical and Experimental Sciences, Brescia University, Brescia, Italy.

University of Groningen, European Research Institute for the Biology of Aging, University Medical Center Groningen, Groningen, Netherlands; Lebanese University, Doctoral School of Science and Technology, Hadath, Beirut, Lebanon.

出版信息

Mech Ageing Dev. 2018 Dec;176:19-23. doi: 10.1016/j.mad.2018.10.005. Epub 2018 Nov 3.

DOI:10.1016/j.mad.2018.10.005
PMID:30395873
Abstract

Cellular senescence is a state of irreversible growth arrest characterized by hypertrophy and secretion of various bioactive molecules, a phenomenon defined the Senescence-Associated Secretory Phenotype (SASP). Senescent cells are implicated in a number of biological functions, from embryogenesis to aging. Significantly, excessive accumulation of senescent cells is associated to a decline of regenerative capacity and chronic inflammation. In accordance, the removal of senescent cells is sufficient to delay several pathologies and promote healthspan. Calorie restriction (CR) without malnutrition is currently the most effective non-genetic intervention to delay aging phenotypes. Recently, we have shown that CR can prevent accumulation of senescent cells in both mice and humans. Here, we summarize the current knowledge on the molecular and cellular events associated with CR, and define how these events can interfere with the induction of cellular senescence. We discuss the potential side effects of preventing senescence, and the possible alternative dietary interventions with potential senolytic properties.

摘要

细胞衰老(Cellular senescence)是一种不可逆的生长停滞状态,其特征是细胞肥大和各种生物活性分子的分泌,这一现象被定义为衰老相关分泌表型(Senescence-Associated Secretory Phenotype,SASP)。衰老细胞参与了许多生物学功能,从胚胎发生到衰老。重要的是,衰老细胞的过度积累与再生能力下降和慢性炎症有关。因此,清除衰老细胞足以延缓多种疾病并促进健康寿命。目前,限制热量摄入(Calorie restriction,CR)而不造成营养不良是延缓衰老表型的最有效非遗传干预措施。最近,我们已经表明 CR 可以防止小鼠和人类衰老细胞的积累。在这里,我们总结了与 CR 相关的分子和细胞事件的最新知识,并定义了这些事件如何干扰细胞衰老的诱导。我们讨论了预防衰老的潜在副作用,以及具有潜在衰老细胞溶解特性的可能替代饮食干预措施。

相似文献

1
Caloric restriction and cellular senescence.热量限制与细胞衰老。
Mech Ageing Dev. 2018 Dec;176:19-23. doi: 10.1016/j.mad.2018.10.005. Epub 2018 Nov 3.
2
The effects of graded caloric restriction: XII. Comparison of mouse to human impact on cellular senescence in the colon.热量限制的影响:十二、小鼠与人结肠细胞衰老的比较。
Aging Cell. 2018 Jun;17(3):e12746. doi: 10.1111/acel.12746. Epub 2018 Mar 25.
3
Cellular Senescence: A Translational Perspective.细胞衰老:转化视角。
EBioMedicine. 2017 Jul;21:21-28. doi: 10.1016/j.ebiom.2017.04.013. Epub 2017 Apr 12.
4
Targeting cellular senescence based on interorganelle communication, multilevel proteostasis, and metabolic control.基于细胞器间通讯、多层次蛋白质稳态和代谢控制靶向细胞衰老。
FEBS J. 2021 Jun;288(12):3834-3854. doi: 10.1111/febs.15631. Epub 2020 Dec 8.
5
Methionine restriction delays senescence and suppresses the senescence-associated secretory phenotype in the kidney through endogenous hydrogen sulfide.蛋氨酸限制通过内源性硫化氢延缓肾脏衰老并抑制衰老相关分泌表型。
Cell Cycle. 2019 Jul;18(14):1573-1587. doi: 10.1080/15384101.2019.1618124. Epub 2019 Jun 5.
6
Emerging role of extracellular vesicles as a senescence-associated secretory phenotype: Insights into the pathophysiology of lung diseases.细胞外囊泡作为衰老相关分泌表型的新兴作用:对肺部疾病病理生理学的认识。
Mol Aspects Med. 2018 Apr;60:92-103. doi: 10.1016/j.mam.2017.11.005. Epub 2017 Nov 20.
7
Targeting Senescent Cells: Possible Implications for Delaying Skin Aging: A Mini-Review.靶向衰老细胞:对延缓皮肤衰老的潜在影响:一篇综述短文
Gerontology. 2016;62(5):513-8. doi: 10.1159/000444877. Epub 2016 Apr 1.
8
Reducing Senescent Cell Burden in Aging and Disease.减少衰老和疾病中的衰老细胞负担。
Trends Mol Med. 2020 Jul;26(7):630-638. doi: 10.1016/j.molmed.2020.03.005. Epub 2020 Apr 17.
9
Metallothioneins, ageing and cellular senescence: a future therapeutic target.金属硫蛋白、衰老和细胞衰老:未来的治疗靶点。
Curr Pharm Des. 2013;19(9):1753-64.
10
Senescence and the SASP: many therapeutic avenues.衰老和 SASP:多种治疗途径。
Genes Dev. 2020 Dec 1;34(23-24):1565-1576. doi: 10.1101/gad.343129.120.

引用本文的文献

1
Calorie restriction mimetics against aging and inflammation.抗老化和抗炎的卡路里限制模拟物。
Biogerontology. 2025 Jun 24;26(4):126. doi: 10.1007/s10522-025-10269-0.
2
Potential downsides of calorie restriction.热量限制的潜在不利之处。
Nat Rev Endocrinol. 2025 Apr 17. doi: 10.1038/s41574-025-01111-1.
3
Cellular Senescence in Health, Disease, and Lens Aging.健康、疾病与晶状体衰老中的细胞衰老
Pharmaceuticals (Basel). 2025 Feb 12;18(2):244. doi: 10.3390/ph18020244.
4
The brain-body energy conservation model of aging.衰老的脑体能量守恒模型。
Nat Aging. 2024 Oct;4(10):1354-1371. doi: 10.1038/s43587-024-00716-x. Epub 2024 Oct 8.
5
Therapeutic targeting of senescent cells in the CNS.中枢神经系统衰老细胞的治疗靶向。
Nat Rev Drug Discov. 2024 Nov;23(11):817-837. doi: 10.1038/s41573-024-01033-z. Epub 2024 Sep 30.
6
The Role of Molecular and Cellular Aging Pathways on Age-Related Hearing Loss.分子和细胞衰老途径在与年龄相关的听力损失中的作用。
Int J Mol Sci. 2024 Sep 7;25(17):9705. doi: 10.3390/ijms25179705.
7
Evaluating the impact of caloric restriction, body mass index and exercise on primary open-angle glaucoma: A review.评估热量限制、体重指数和运动对原发性开角型青光眼的影响:一项综述。
Eur J Ophthalmol. 2025 Mar;35(2):429-440. doi: 10.1177/11206721241274445. Epub 2024 Aug 22.
8
Cellular Senescence and Extracellular Vesicles in the Pathogenesis and Treatment of Obesity-A Narrative Review.细胞衰老与细胞外囊泡在肥胖发病机制及治疗中的作用:综述
Int J Mol Sci. 2024 Jul 20;25(14):7943. doi: 10.3390/ijms25147943.
9
Senotherapeutics to Counteract Senescent Cells Are Prominent Topics in the Context of Anti-Ageing Strategies.衰老细胞的治疗策略是抗衰老策略中的重要课题。
Int J Mol Sci. 2024 Feb 1;25(3):1792. doi: 10.3390/ijms25031792.
10
New Possibilities for Evaluating the Development of Age-Related Pathologies Using the Dynamical Network Biomarkers Theory.利用动态网络生物标志物理论评估与年龄相关的病理发展的新可能性。
Cells. 2023 Sep 17;12(18):2297. doi: 10.3390/cells12182297.