• 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

辛伐他汀对血管内皮细胞的抗老化作用。

Antiaging effects of simvastatin on vascular endothelial cells.

作者信息

Lei Junping, Gu Xiaosong, Ye Zhong, Shi Jianbo, Zheng Xing

机构信息

1Department of Cardiovascular Diseases, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.

出版信息

Clin Appl Thromb Hemost. 2014 Mar;20(2):212-8. doi: 10.1177/1076029612458967. Epub 2012 Sep 9.

DOI:10.1177/1076029612458967
PMID:22964779
Abstract

The anti-inflammatory, antioxidative, and antiarteriosclerosis activities of simvastatin along with its protective effects on the endothelium suggest that it may also have antiaging effects. The aim of this study was to investigate the antiaging effects of simvastatin as well as its effects on sirtuin 1 (SIRT1) expression in endothelial cells. Aged rats and human umbilical vein endothelial cells were treated with simvastatin in the presence and absence of oxidized low-density lipoprotein (OX-LDL). Aortic β-galactosidase staining was undertaken to determine senescence, and SIRT1 protein expression was evaluated using Western blot analysis. After simvastatin therapy, arterial endothelial cell aging was significantly reduced, and SIRT1 expression was significantly increased. The OX-LDL significantly accelerated the senescence of umbilical vein endothelial cells and decreased SIRT1 expression. The OX-LDL-induced downregulation of SIRT1 was blocked by simvastatin. Simvastatin treatment also reduced umbilical vein endothelial cell aging and increased SIRT1 expression.

摘要

辛伐他汀的抗炎、抗氧化和抗动脉粥样硬化活性及其对内皮的保护作用表明它可能也具有抗衰老作用。本研究的目的是探讨辛伐他汀的抗衰老作用及其对内皮细胞中沉默调节蛋白1(SIRT1)表达的影响。在存在和不存在氧化型低密度脂蛋白(OX-LDL)的情况下,用辛伐他汀处理老年大鼠和人脐静脉内皮细胞。进行主动脉β-半乳糖苷酶染色以确定衰老,并使用蛋白质印迹分析评估SIRT1蛋白表达。辛伐他汀治疗后,动脉内皮细胞衰老显著减轻,SIRT1表达显著增加。OX-LDL显著加速脐静脉内皮细胞衰老并降低SIRT1表达。辛伐他汀可阻断OX-LDL诱导的SIRT1下调。辛伐他汀治疗还可减轻脐静脉内皮细胞衰老并增加SIRT1表达。

相似文献

1
Antiaging effects of simvastatin on vascular endothelial cells.辛伐他汀对血管内皮细胞的抗老化作用。
Clin Appl Thromb Hemost. 2014 Mar;20(2):212-8. doi: 10.1177/1076029612458967. Epub 2012 Sep 9.
2
Statins modulate oxidized low-density lipoprotein-mediated adhesion molecule expression in human coronary artery endothelial cells: role of LOX-1.他汀类药物调节氧化型低密度脂蛋白介导的人冠状动脉内皮细胞黏附分子表达:凝集素样氧化型低密度脂蛋白受体1的作用
J Pharmacol Exp Ther. 2002 Aug;302(2):601-5. doi: 10.1124/jpet.102.034959.
3
Visfatin attenuates the ox-LDL-induced senescence of endothelial progenitor cells by upregulating SIRT1 expression through the PI3K/Akt/ERK pathway.内脂素通过PI3K/Akt/ERK途径上调SIRT1表达,减轻氧化型低密度脂蛋白诱导的内皮祖细胞衰老。
Int J Mol Med. 2016 Aug;38(2):643-9. doi: 10.3892/ijmm.2016.2633. Epub 2016 Jun 9.
4
D-4F, an apolipoprotein A-I mimetic peptide, protects human umbilical vein endothelial cells from oxidized low-density lipoprotein-induced injury by preventing the downregulation of pigment epithelium-derived factor expression.D-4F是一种载脂蛋白A-I模拟肽,通过防止色素上皮衍生因子表达下调,保护人脐静脉内皮细胞免受氧化型低密度脂蛋白诱导的损伤。
J Cardiovasc Pharmacol. 2014 Jun;63(6):553-61. doi: 10.1097/FJC.0000000000000080.
5
Oxidized low-density lipoprotein induces endothelial progenitor cell senescence, leading to cellular dysfunction.氧化型低密度脂蛋白诱导内皮祖细胞衰老,导致细胞功能障碍。
Clin Exp Pharmacol Physiol. 2004 Jul;31(7):407-13. doi: 10.1111/j.1440-1681.2004.04022.x.
6
Myeloperoxidase-derived hypochlorous acid promotes ox-LDL-induced senescence of endothelial cells through a mechanism involving β-catenin signaling in hyperlipidemia.髓过氧化物酶衍生的次氯酸通过一种涉及高脂血症中β-连环蛋白信号传导的机制促进氧化型低密度脂蛋白诱导的内皮细胞衰老。
Biochem Biophys Res Commun. 2015 Nov 27;467(4):859-65. doi: 10.1016/j.bbrc.2015.10.053. Epub 2015 Oct 22.
7
SIRT1 regulates accumulation of oxidized LDL in HUVEC via the autophagy-lysosomal pathway.沉默调节蛋白1通过自噬-溶酶体途径调节人脐静脉内皮细胞中氧化型低密度脂蛋白的积累。
Prostaglandins Other Lipid Mediat. 2016 Jan;122:37-44. doi: 10.1016/j.prostaglandins.2015.12.005. Epub 2015 Dec 23.
8
Resveratrol Enhances Autophagic Flux and Promotes Ox-LDL Degradation in HUVECs via Upregulation of SIRT1.白藜芦醇通过上调SIRT1增强人脐静脉内皮细胞的自噬通量并促进氧化型低密度脂蛋白的降解。
Oxid Med Cell Longev. 2016;2016:7589813. doi: 10.1155/2016/7589813. Epub 2016 Mar 16.
9
Induction of endothelial nitric oxide synthase, SIRT1, and catalase by statins inhibits endothelial senescence through the Akt pathway.通过 Akt 通路,他汀类药物诱导内皮型一氧化氮合酶、SIRT1 和过氧化氢酶,从而抑制内皮细胞衰老。
Arterioscler Thromb Vasc Biol. 2010 Nov;30(11):2205-11. doi: 10.1161/ATVBAHA.110.210500. Epub 2010 Aug 12.
10
Adverse balance of nitric oxide/peroxynitrite in the dysfunctional endothelium can be reversed by statins.功能失调的内皮中一氧化氮/过氧亚硝酸盐的不良平衡可通过他汀类药物逆转。
J Cardiovasc Pharmacol. 2007 Oct;50(4):391-8. doi: 10.1097/FJC.0b013e31811f3fd0.

引用本文的文献

1
FLRT2 prevents endothelial cell senescence and vascular aging by regulating the ITGB4/mTORC2/p53 signaling pathway.FLRT2 通过调控 ITGB4/mTORC2/p53 信号通路预防血管内皮细胞衰老和血管老化。
JCI Insight. 2024 Apr 8;9(7):e172678. doi: 10.1172/jci.insight.172678.
2
Lipophilic Statins Eliminate Senescent Endothelial Cells by inducing Anoikis-Related Cell Death.疏水性他汀类药物通过诱导与失巢凋亡相关的细胞死亡来清除衰老的内皮细胞。
Cells. 2023 Dec 14;12(24):2836. doi: 10.3390/cells12242836.
3
Evaluation of Rosuvastatin Therapy on Gene Expression in Patients with Multiple Sclerosis: An Uncontrolled Clinical Trial.
瑞舒伐他汀治疗对多发性硬化症患者基因表达的评估:一项非对照临床试验。
Curr Ther Res Clin Exp. 2023 Sep 30;99:100718. doi: 10.1016/j.curtheres.2023.100718. eCollection 2023.
4
PCSK9 attenuates efferocytosis in endothelial cells and promotes vascular aging.PCSK9 可减弱内皮细胞的胞噬作用,并促进血管老化。
Theranostics. 2023 May 11;13(9):2914-2929. doi: 10.7150/thno.83914. eCollection 2023.
5
Network Analysis Reveals the Molecular Bases of Statin Pleiotropy That Vary with Genetic Background.网络分析揭示了随遗传背景而异的他汀类药物多效性的分子基础。
Microbiol Spectr. 2023 Mar 22;11(2):e0414822. doi: 10.1128/spectrum.04148-22.
6
Regulatory Effects of Statins on SIRT1 and Other Sirtuins in Cardiovascular Diseases.他汀类药物对心血管疾病中SIRT1及其他沉默调节蛋白的调控作用
Life (Basel). 2022 May 20;12(5):760. doi: 10.3390/life12050760.
7
Combination therapy of lovastatin and AMP-activated protein kinase activator improves mitochondrial and peroxisomal functions and clinical disease in experimental autoimmune encephalomyelitis model.洛伐他汀与 AMP 激活蛋白激酶激活剂联合治疗改善实验性自身免疫性脑脊髓炎模型中的线粒体和过氧化物酶体功能及临床疾病。
Immunology. 2018 Jul;154(3):434-451. doi: 10.1111/imm.12893. Epub 2018 Feb 8.
8
Fibroblast growth factor 21 delayed endothelial replicative senescence and protected cells from HO-induced premature senescence through SIRT1.成纤维细胞生长因子21通过沉默信息调节因子1延缓内皮细胞复制性衰老,并保护细胞免受过氧化氢诱导的早衰。
Am J Transl Res. 2017 Oct 15;9(10):4492-4501. eCollection 2017.
9
Exercise intervention attenuates hyperhomocysteinemia-induced aortic endothelial oxidative injury by regulating SIRT1 through mitigating NADPH oxidase/LOX-1 signaling.运动干预通过减轻 NADPH 氧化酶/LOX-1 信号通路来调节 SIRT1,从而减轻高同型半胱氨酸血症引起的主动脉内皮氧化损伤。
Redox Biol. 2018 Apr;14:116-125. doi: 10.1016/j.redox.2017.08.016. Epub 2017 Aug 24.
10
SIRT1 inhibition causes oxidative stress and inflammation in patients with coronary artery disease.沉默调节蛋白1抑制会在冠心病患者中引发氧化应激和炎症。
Redox Biol. 2017 Oct;13:301-309. doi: 10.1016/j.redox.2017.05.027. Epub 2017 Jun 2.