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Molecular markers of cardiovascular damage in hypertension

Articolo
Data di Pubblicazione:
2013
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. © 2013 Bentham Science Publishers.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Hypertension; Oxidative stress; Telomerase; Telomere
Elenco autori:
Andreassi, Mariagrazia
Autori di Ateneo:
ANDREASSI MARIAGRAZIA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/298249
Pubblicato in:
CURRENT PHARMACEUTICAL DESIGN
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-84877824845&origin=inward
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