• 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

靶向NAD⁺:这是延缓心脏衰老的常见策略吗?

Targeting NAD+: is it a common strategy to delay heart aging?

作者信息

Yuan Yang, Liang Bing, Liu Xin-Lin, Liu Wen-Jing, Huang Bing-Huan, Yang Shan-Bo, Gao Yuan-Zhen, Meng Jing-Sen, Li Meng-Jiao, Ye Ting, Wang Chuan-Zhi, Hu Xiao-Kun, Xing Dong-Ming

机构信息

Cancer Institute of The Affiliated Hospital of Qingdao University and Qingdao Cancer Institute, Qingdao, China.

Interventional Medicine Center, Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Cell Death Discov. 2022 Apr 26;8(1):230. doi: 10.1038/s41420-022-01031-3.

DOI:10.1038/s41420-022-01031-3
PMID:35474295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9042931/
Abstract

Heart aging is the main susceptible factor to coronary heart disease and significantly increases the risk of heart failure, especially when the aging heart is suffering from ischemia-reperfusion injury. Numerous studies with NAD+ supplementations have suggested its use in anti-aging treatment. However, systematic reviews regarding the overall role of NAD+ in cardiac aging are scarce. The relationship between NAD+ signaling and heart aging has yet to be clarified. This review comprehensively summarizes the current studies on the role of NAD+ signaling in delaying heart aging from the following aspects: the influence of NAD+ supplementations on the aging heart; the relationship and cross-talks between NAD+ signaling and other cardiac aging-related signaling pathways; Importantly, the therapeutic potential of targeting NAD+ in delaying heart aging will be discussed. In brief, NAD+ plays a vital role in delaying heart aging. However, the abnormalities such as altered glucose and lipid metabolism, oxidative stress, and calcium overload could also interfere with NAD+ function in the heart. Therefore, the specific physiopathology of the aging heart should be considered before applying NAD+ supplementations. We believe that this article will help augment our understanding of heart aging mechanisms. In the meantime, it provides invaluable insights into possible therapeutic strategies for preventing age-related heart diseases in clinical settings.

摘要

心脏衰老(心脏老化)是冠心病的主要易感因素,会显著增加心力衰竭的风险,尤其是当衰老的心脏遭受缺血再灌注损伤时。大量关于补充烟酰胺腺嘌呤二核苷酸(NAD+)的研究表明其可用于抗衰老治疗。然而,关于NAD+在心脏衰老中的整体作用的系统综述却很匮乏。NAD+信号传导与心脏衰老之间的关系尚未阐明。本综述从以下几个方面全面总结了目前关于NAD+信号传导在延缓心脏衰老中作用的研究:补充NAD+对衰老心脏的影响;NAD+信号传导与其他心脏衰老相关信号通路之间的关系及相互作用;重要的是,还将讨论靶向NAD+在延缓心脏衰老方面的治疗潜力。简而言之,NAD+在延缓心脏衰老中起着至关重要的作用。然而,葡萄糖和脂质代谢改变、氧化应激和钙超载等异常情况也可能干扰心脏中的NAD+功能。因此,在应用NAD+补充剂之前应考虑衰老心脏的具体病理生理学。我们相信本文将有助于加深我们对心脏衰老机制的理解。同时,它为临床环境中预防与年龄相关的心脏病的可能治疗策略提供了宝贵的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/4235ee384913/41420_2022_1031_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/38a391128ef9/41420_2022_1031_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/42f93ad16326/41420_2022_1031_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/bd540b51fef8/41420_2022_1031_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/a6dd9df915c3/41420_2022_1031_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/4235ee384913/41420_2022_1031_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/38a391128ef9/41420_2022_1031_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/42f93ad16326/41420_2022_1031_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/bd540b51fef8/41420_2022_1031_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/a6dd9df915c3/41420_2022_1031_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c2d/9042931/4235ee384913/41420_2022_1031_Fig5_HTML.jpg

相似文献

1
Targeting NAD+: is it a common strategy to delay heart aging?靶向NAD⁺:这是延缓心脏衰老的常见策略吗?
Cell Death Discov. 2022 Apr 26;8(1):230. doi: 10.1038/s41420-022-01031-3.
2
NAD Deficiency Is a Common Central Pathological Factor of a Number of Diseases and Aging: Mechanisms and Therapeutic Implications.NAD 缺乏是多种疾病和衰老的常见中枢病理因素:机制和治疗意义。
Antioxid Redox Signal. 2019 Feb 20;30(6):890-905. doi: 10.1089/ars.2017.7445. Epub 2018 Feb 7.
3
Implications of NAD Metabolism in the Aging Retina and Retinal Degeneration.NAD 代谢对衰老视网膜和视网膜变性的影响。
Oxid Med Cell Longev. 2020 May 9;2020:2692794. doi: 10.1155/2020/2692794. eCollection 2020.
4
Kynurenine pathway, NAD synthesis, and mitochondrial function: Targeting tryptophan metabolism to promote longevity and healthspan.犬尿氨酸途径、NAD 合成和线粒体功能:靶向色氨酸代谢以促进长寿和健康寿命。
Exp Gerontol. 2020 Apr;132:110841. doi: 10.1016/j.exger.2020.110841. Epub 2020 Jan 16.
5
NAD and the aging process: Role in life, death and everything in between.NAD 与衰老过程:在生命、死亡及其间的一切中的作用。
Mol Cell Endocrinol. 2017 Nov 5;455:62-74. doi: 10.1016/j.mce.2016.11.003. Epub 2016 Nov 5.
6
Oxidative stress and NAD+ in ischemic brain injury: current advances and future perspectives.氧化应激与缺血性脑损伤中的 NAD+:当前进展与未来展望。
Curr Med Chem. 2010;17(20):2152-8. doi: 10.2174/092986710791299911.
7
Exogenous supplemental NAD+ protect myocardium against myocardial ischemic/reperfusion injury in swine model.外源性补充烟酰胺腺嘌呤二核苷酸(NAD+)可在猪模型中保护心肌免受心肌缺血/再灌注损伤。
Am J Transl Res. 2019 Sep 15;11(9):6066-6074. eCollection 2019.
8
Interaction of cardiovascular risk factors with myocardial ischemia/reperfusion injury, preconditioning, and postconditioning.心血管危险因素与心肌缺血/再灌注损伤、预处理及后处理之间的相互作用。
Pharmacol Rev. 2007 Dec;59(4):418-58. doi: 10.1124/pr.107.06002. Epub 2007 Nov 29.
9
Nicotinamide Mononucleotide: A Promising Molecule for Therapy of Diverse Diseases by Targeting NAD+ Metabolism.烟酰胺单核苷酸:一种通过靶向烟酰胺腺嘌呤二核苷酸(NAD+)代谢治疗多种疾病的有前景的分子。
Front Cell Dev Biol. 2020 Apr 28;8:246. doi: 10.3389/fcell.2020.00246. eCollection 2020.
10
Exogenous nicotinamide adenine dinucleotide administration alleviates ischemia/reperfusion-induced oxidative injury in isolated rat hearts via Sirt5-SDH-succinate pathway.外源性烟酰胺腺嘌呤二核苷酸给药通过 Sirt5-SDH-琥珀酸途径减轻离体大鼠心脏缺血/再灌注诱导的氧化损伤。
Eur J Pharmacol. 2019 Sep 5;858:172520. doi: 10.1016/j.ejphar.2019.172520. Epub 2019 Jul 3.

引用本文的文献

1
Metabolic Regulation of Cardiovascular Aging.心血管衰老的代谢调节
Curr Cardiol Rep. 2025 Aug 15;27(1):128. doi: 10.1007/s11886-025-02279-8.
2
Mechanisms of endothelial senescence and vascular aging.内皮细胞衰老与血管老化的机制。
Biogerontology. 2025 Jun 25;26(4):128. doi: 10.1007/s10522-025-10279-y.
3
Nicotinamide Mononucleotide (NMN) Improves the Senescence of Mouse Vascular Smooth Muscle Cells Induced by Ang II Through Activating p-AMPK/KLF4 Pathway.烟酰胺单核苷酸(NMN)通过激活p-AMPK/KLF4信号通路改善血管紧张素II诱导的小鼠血管平滑肌细胞衰老。

本文引用的文献

1
Petri Net modelling approach for analysing the behaviour of [inline-formula removed] and signalling pathways in arrhythmogenic right ventricular cardiomyopathy.利用 Petri 网模型分析致心律失常性右室心肌病中 [inline-formula removed] 和信号通路的行为。
IET Syst Biol. 2020 Dec;14(6):350-367. doi: 10.1049/iet-syb.2020.0038.
2
Increased demand for NAD relative to ATP drives aerobic glycolysis.与 ATP 相比,NAD 的需求增加会促使有氧糖酵解。
Mol Cell. 2021 Feb 18;81(4):691-707.e6. doi: 10.1016/j.molcel.2020.12.012. Epub 2020 Dec 30.
3
Parkin overexpression alleviates cardiac aging through facilitating K63-polyubiquitination of TBK1 to facilitate mitophagy.
Pharmaceuticals (Basel). 2025 Apr 9;18(4):553. doi: 10.3390/ph18040553.
4
Pleozymes: Pleiotropic Oxidized Carbon Nanozymes Enhance Cellular Metabolic Flexibility.多效酶:多效性氧化碳纳米酶增强细胞代谢灵活性。
Nanomaterials (Basel). 2024 Dec 15;14(24):2017. doi: 10.3390/nano14242017.
5
Systemic aging fuels heart failure: Molecular mechanisms and therapeutic avenues.全身衰老引发心力衰竭:分子机制与治疗途径
ESC Heart Fail. 2025 Apr;12(2):1059-1080. doi: 10.1002/ehf2.14947. Epub 2024 Jul 22.
6
Loss of cardiac mitochondrial complex I persulfidation impairs NAD homeostasis in aging.心脏线粒体复合物 I 过硫化损失导致衰老中心脏 NAD 稳态失衡。
Redox Biol. 2024 Feb;69:103014. doi: 10.1016/j.redox.2023.103014. Epub 2023 Dec 25.
7
Fingerstick blood assay maps real-world NAD disparity across gender and age.指尖采血检测绘制出真实世界中 NAD 性别和年龄差异图谱。
Aging Cell. 2023 Oct;22(10):e13965. doi: 10.1111/acel.13965. Epub 2023 Aug 28.
8
Preclinical multi-target strategies for myocardial ischemia-reperfusion injury.心肌缺血再灌注损伤的临床前多靶点策略
Front Cardiovasc Med. 2022 Aug 22;9:967115. doi: 10.3389/fcvm.2022.967115. eCollection 2022.
帕金蛋白的过表达通过促进TBK1的K63-多聚泛素化以促进线粒体自噬来减轻心脏衰老。
Biochim Biophys Acta Mol Basis Dis. 2021 Jan 1;1867(1):165997. doi: 10.1016/j.bbadis.2020.165997. Epub 2020 Oct 22.
4
Activation of toll like receptor 4 (TLR4) promotes cardiomyocyte apoptosis through SIRT2 dependent p53 deacetylation.Toll 样受体 4(TLR4)的激活通过 SIRT2 依赖性 p53 去乙酰化促进心肌细胞凋亡。
Sci Rep. 2020 Nov 6;10(1):19232. doi: 10.1038/s41598-020-75301-4.
5
TIGAR reduces smooth muscle cell autophagy to prevent pulmonary hypertension.TIGAR 减少平滑肌细胞自噬以预防肺动脉高压。
Am J Physiol Heart Circ Physiol. 2020 Nov 1;319(5):H1087-H1096. doi: 10.1152/ajpheart.00314.2020. Epub 2020 Sep 18.
6
Inflammageing in the cardiovascular system: mechanisms, emerging targets, and novel therapeutic strategies.心血管系统中的炎症衰老:机制、新靶点和新的治疗策略。
Clin Sci (Lond). 2020 Sep 18;134(17):2243-2262. doi: 10.1042/CS20191213.
7
Impact of Short-Term Hypoxia on Sirtuins as Regulatory Elements in HUVECs.短期缺氧对人脐静脉内皮细胞中作为调节元件的沉默调节蛋白的影响。
J Clin Med. 2020 Aug 11;9(8):2604. doi: 10.3390/jcm9082604.
8
Blood NAD levels are reduced in very old patients hospitalized for heart failure.血液 NAD 水平在因心力衰竭住院的非常老的患者中降低。
Exp Gerontol. 2020 Oct 1;139:111051. doi: 10.1016/j.exger.2020.111051. Epub 2020 Aug 9.
9
SS-31 and NMN: Two paths to improve metabolism and function in aged hearts.SS-31 和 NMN:改善衰老心脏代谢和功能的两条途径。
Aging Cell. 2020 Oct;19(10):e13213. doi: 10.1111/acel.13213. Epub 2020 Aug 11.
10
Macrophage Immunometabolism and Inflammaging: Roles of Mitochondrial Dysfunction, Cellular Senescence, CD38, and NAD.巨噬细胞免疫代谢与炎症衰老:线粒体功能障碍、细胞衰老、CD38和烟酰胺腺嘌呤二核苷酸的作用
Immunometabolism. 2020;2(3):e200026. doi: 10.20900/immunometab20200026. Epub 2020 Jul 1.