Suppr超能文献

内皮功能障碍和血管老化中的血流动力。

Hemodynamic forces in endothelial dysfunction and vascular aging.

机构信息

Department of Cell and Molecular Physiology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Exp Gerontol. 2011 Feb-Mar;46(2-3):185-8. doi: 10.1016/j.exger.2010.09.010. Epub 2010 Oct 1.

Abstract

Aging is a key risk factor associated with the onset of cardiovascular disease. Notably, vascular aging and cardiovascular disease are both associated with endothelial dysfunction, or a marked decrease in production and bioavailability the vasodilator of nitric oxide (NO). As a result of decreased nitric oxide availability, aging vessels often exhibit endothelial cell senescence and increased oxidative stress. One of the most potent activators of NO production is fluid shear stress produced by blood flow. Interestingly, age-related decrease in NO production partially results from endothelial insensitivity to shear stress. While the endothelial cell response to fluid shear stress has been well characterized in recent years, the exact mechanisms of how the mechanical force of fluid shear stress is converted into intracellular biochemical signals are relatively unknown. Therefore, gaining a better knowledge of mechanosignaling events in endothelial cells may prove to be beneficial for developing potential therapies for cardiovascular diseases.

摘要

衰老是与心血管疾病发病相关的一个关键风险因素。值得注意的是,血管衰老和心血管疾病都与内皮功能障碍有关,即血管舒张因子一氧化氮(NO)的产生和生物利用度显著下降。由于一氧化氮供应减少,衰老的血管常常表现出内皮细胞衰老和氧化应激增加。促进一氧化氮产生的最有效物质之一是血流产生的流体切应力。有趣的是,与年龄相关的 NO 产生减少部分是由于内皮细胞对切应力不敏感。虽然近年来已经很好地描述了内皮细胞对流体切应力的反应,但将流体切应力的机械力转化为细胞内生化信号的确切机制尚不清楚。因此,更好地了解内皮细胞中的机械信号事件可能有助于开发心血管疾病的潜在治疗方法。

相似文献

1
Hemodynamic forces in endothelial dysfunction and vascular aging.
Exp Gerontol. 2011 Feb-Mar;46(2-3):185-8. doi: 10.1016/j.exger.2010.09.010. Epub 2010 Oct 1.
2
Integrating molecular and cellular components of endothelial shear stress mechanotransduction.
Am J Physiol Heart Circ Physiol. 2024 Oct 1;327(4):H989-H1003. doi: 10.1152/ajpheart.00431.2024. Epub 2024 Aug 23.
3
Hemodynamic shear stress and the endothelium in cardiovascular pathophysiology.
Nat Clin Pract Cardiovasc Med. 2009 Jan;6(1):16-26. doi: 10.1038/ncpcardio1397. Epub 2008 Nov 25.
6
Biophysical and Biochemical Roles of Shear Stress on Endothelium: A Revisit and New Insights.
Circ Res. 2025 Mar 28;136(7):752-772. doi: 10.1161/CIRCRESAHA.124.325685. Epub 2025 Mar 27.
7
Fluid shear stress and the vascular endothelium: for better and for worse.
Prog Biophys Mol Biol. 2003 Apr;81(3):177-99. doi: 10.1016/s0079-6107(02)00052-4.
8
Endothelial dysfunction and aging: an update.
Ageing Res Rev. 2010 Apr;9(2):142-52. doi: 10.1016/j.arr.2009.07.002. Epub 2009 Jul 18.
9
Endothelial Response to Pathophysiological Stress.
Arterioscler Thromb Vasc Biol. 2019 Nov;39(11):e233-e243. doi: 10.1161/ATVBAHA.119.312580. Epub 2019 Oct 23.
10
Cellular and molecular biology of aging endothelial cells.
J Mol Cell Cardiol. 2015 Dec;89(Pt B):122-35. doi: 10.1016/j.yjmcc.2015.01.021. Epub 2015 Feb 2.

引用本文的文献

2
Premature aging in genetic diseases: what conclusions can be drawn for physiological aging.
Front Aging. 2024 Feb 28;4:1327833. doi: 10.3389/fragi.2023.1327833. eCollection 2023.
4
Role of blood flow in endothelial functionality: a review.
Front Cell Dev Biol. 2023 Oct 13;11:1259280. doi: 10.3389/fcell.2023.1259280. eCollection 2023.
5
Premature senescence and cardiovascular disease following cancer treatments: mechanistic insights.
Front Cardiovasc Med. 2023 Sep 14;10:1212174. doi: 10.3389/fcvm.2023.1212174. eCollection 2023.
7
m6A Modification Mediates Endothelial Cell Responses to Oxidative Stress in Vascular Aging Induced by Low Fluid Shear Stress.
Oxid Med Cell Longev. 2023 Jan 27;2023:8134027. doi: 10.1155/2023/8134027. eCollection 2023.
8
Targeting Immune Senescence in Atherosclerosis.
Int J Mol Sci. 2022 Oct 27;23(21):13059. doi: 10.3390/ijms232113059.
9

本文引用的文献

1
L-arginine as a nutritional prophylaxis against vascular endothelial dysfunction with aging.
J Cardiovasc Pharmacol Ther. 2010 Mar;15(1):17-23. doi: 10.1177/1074248409354599. Epub 2010 Jan 6.
2
The effect of physical exercise on endothelial function.
Sports Med. 2009;39(10):797-812. doi: 10.2165/11317750-000000000-00000.
3
Roles of oxidative stress and redox regulation in atherosclerosis.
J Atheroscler Thromb. 2009 Oct;16(5):532-8. doi: 10.5551/jat.1255. Epub 2009 Sep 14.
4
Aging impairs flow-induced dilation in coronary arterioles: role of NO and H(2)O(2).
Am J Physiol Heart Circ Physiol. 2009 Sep;297(3):H1087-95. doi: 10.1152/ajpheart.00356.2009. Epub 2009 Jul 17.
5
Oxidative stress in vascular disease: causes, defense mechanisms and potential therapies.
Nat Clin Pract Cardiovasc Med. 2008 Jun;5(6):338-49. doi: 10.1038/ncpcardio1211. Epub 2008 May 6.
7
Vascular cell senescence: contribution to atherosclerosis.
Circ Res. 2007 Jan 5;100(1):15-26. doi: 10.1161/01.RES.0000256837.40544.4a.
8
G protein-coupled receptors sense fluid shear stress in endothelial cells.
Proc Natl Acad Sci U S A. 2006 Oct 17;103(42):15463-8. doi: 10.1073/pnas.0607224103. Epub 2006 Oct 9.
9
Role of small GTPases in endothelial cytoskeletal dynamics and the shear stress response.
Circ Res. 2006 Feb 3;98(2):176-85. doi: 10.1161/01.RES.0000200162.94463.d7.
10
A mechanosensory complex that mediates the endothelial cell response to fluid shear stress.
Nature. 2005 Sep 15;437(7057):426-31. doi: 10.1038/nature03952.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验