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高血压患者心血管损伤的分子标志物。

Molecular markers of cardiovascular damage in hypertension.

机构信息

Cardiovascular Research Laboratory, Cardiac Thoracic and Vascular Department-University of Pisa, Via Paradisa 2 56 124 Pisa, Italy.

出版信息

Curr Pharm Des. 2013;19(13):2341-50. doi: 10.2174/1381612811319130002.

DOI:10.2174/1381612811319130002
PMID:23173583
Abstract

There is increasing evidence that an elevation of oxidative stress and associated oxidative damages are mediators of vascular injury in various cardiovascular pathologies, including hypertension. Accumulation of oxidative damage is thought to play an important role in aging and age-associated diseases such as hypertension and oxidative stress may function as a common trigger for activation of the senescence programme. In this regard, the role of telomeres in the onset, development and prognosis of hypertension has generated considerable interest. These structures may deteriorate in the onset and development of arterial hypertension in which their length may be a predictor of outcome. As telomere length by its nature is a marker of cell senescence, this parameter is of particular interest when studying the lifespan and fate of endothelial cells, cardiomyocytes and smooth muscle cells, especially so because telomere length seems to be regulated by various factors notably certain cardiovascular risk factors, such as smoking, sex and obesity that are associated with high levels of oxidative stress. This review focuses on the vascular effects of reactive oxygen species and the role of oxidative stress in hypertension- associated vascular damage. In addition it reviewes the considerable amount of data published recently on the role of telomeres to gain insights into the links between telomere length and hypertension, and assesses the usefulness of telomere length as a new marker of cardiovascular risk.

摘要

越来越多的证据表明,氧化应激升高及其相关的氧化损伤是多种心血管疾病(包括高血压)中血管损伤的介质。氧化损伤的积累被认为在衰老和与衰老相关的疾病中发挥重要作用,如高血压,氧化应激可能作为衰老程序激活的共同触发因素。在这方面,端粒在高血压的发生、发展和预后中的作用引起了相当大的兴趣。这些结构可能在动脉高血压的发生和发展中恶化,其长度可能是预后的预测指标。由于端粒长度本质上是细胞衰老的标志物,因此当研究内皮细胞、心肌细胞和平滑肌细胞的寿命和命运时,这个参数特别有趣,特别是因为端粒长度似乎受到各种因素的调节,特别是某些心血管危险因素,如吸烟、性别和肥胖,这些因素与高水平的氧化应激有关。这篇综述重点介绍了活性氧对血管的影响以及氧化应激在高血压相关血管损伤中的作用。此外,它还回顾了最近发表的大量关于端粒作用的资料,以深入了解端粒长度与高血压之间的联系,并评估端粒长度作为心血管风险的新标志物的有用性。

相似文献

1
Molecular markers of cardiovascular damage in hypertension.高血压患者心血管损伤的分子标志物。
Curr Pharm Des. 2013;19(13):2341-50. doi: 10.2174/1381612811319130002.
2
Telomere length and cardiovascular disease.端粒长度与心血管疾病。
Arch Cardiovasc Dis. 2010 Aug-Sep;103(8-9):454-9. doi: 10.1016/j.acvd.2010.08.002. Epub 2010 Oct 25.
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Does oxidative stress shorten telomeres ? A review.氧化应激会缩短端粒吗?一篇综述。
Biol Lett. 2017 Dec;13(12). doi: 10.1098/rsbl.2017.0463.
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Cellular senescence in endothelial cells from atherosclerotic patients is accelerated by oxidative stress associated with cardiovascular risk factors.来自动脉粥样硬化患者的内皮细胞中的细胞衰老会因与心血管危险因素相关的氧化应激而加速。
Mech Ageing Dev. 2007 Nov-Dec;128(11-12):662-71. doi: 10.1016/j.mad.2007.09.006. Epub 2007 Oct 13.
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Telomere dysfunction in hypertension.高血压中的端粒功能障碍。
J Hypertens. 2007 Nov;25(11):2185-92. doi: 10.1097/HJH.0b013e3282ef6196.
6
Chronology versus biology: telomeres, essential hypertension, and vascular aging.时间顺序与生物学:端粒、原发性高血压和血管衰老
Hypertension. 2002 Sep;40(3):229-32. doi: 10.1161/01.hyp.0000027280.91984.1b.
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Molecular mechanisms of hypertension--reactive oxygen species and antioxidants: a basic science update for the clinician.高血压的分子机制——活性氧和抗氧化剂:临床医生的基础科学更新。
Can J Cardiol. 2012 May;28(3):288-95. doi: 10.1016/j.cjca.2012.01.017. Epub 2012 Mar 23.
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Telomere length is a biomarker of cumulative oxidative stress, biologic age, and an independent predictor of survival and therapeutic treatment requirement associated with smoking behavior.端粒长度是累积氧化应激、生物年龄的生物标志物,也是与吸烟行为相关的生存和治疗需求的独立预测因子。
Am J Ther. 2011 Nov;18(6):e209-26. doi: 10.1097/MJT.0b013e3181cf8ebb.
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Reactive oxygen species in vascular biology: implications in hypertension.血管生物学中的活性氧:对高血压的影响
Histochem Cell Biol. 2004 Oct;122(4):339-52. doi: 10.1007/s00418-004-0696-7. Epub 2004 Aug 26.
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Cellular senescence determines endothelial cell damage induced by uremia.细胞衰老决定了尿毒症引起的内皮细胞损伤。
Exp Gerontol. 2013 Aug;48(8):766-73. doi: 10.1016/j.exger.2013.04.004. Epub 2013 Apr 25.

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Chin Med J (Engl). 2016 Feb 5;129(3):259-66. doi: 10.4103/0366-6999.174491.
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Oxidative Stress State Is Associated with Left Ventricular Mechanics Changes, Measured by Speckle Tracking in Essential Hypertensive Patients.氧化应激状态与原发性高血压患者左心室力学变化相关,通过斑点追踪技术测量。
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