Mechanisms of Arterial Stiffening From Mechanotransduction to Epigenetics

被引:107
作者
Lacolley, Patrick [1 ,2 ]
Regnault, Veronique [1 ,2 ]
Laurent, Stephane [3 ,4 ,5 ]
机构
[1] INSERM, U1116, Vandoeuvre Les Nancy, France
[2] Univ Lorraine, Nancy, France
[3] Hop Europeen Georges Pompidou, AP HP, Dept Pharmacol, Paris, France
[4] INSERM, PARCC, UMR 970, Paris, France
[5] Univ Paris 05, Paris, France
关键词
diabetes mellitus; elastin; oxidative stress; reactive oxygen species; risk factor; PULSE-WAVE VELOCITY; SMOOTH-MUSCLE-CELL; EXTRACELLULAR-MATRIX; HIGH GLUCOSE; HYPERTENSION; STIFFNESS; CALCIFICATION; EXPRESSION; STRESS; HEALTH;
D O I
10.1161/ATVBAHA.119.313129
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Arterial stiffness is a major independent risk factor for cardiovascular complications causing isolated systolic hypertension and increased pulse pressure in the microvasculature of target organs. Stiffening of the arterial wall is determined by common mechanisms including reduced elastin/collagen ratio, production of elastin cross-linking, reactive oxygen species-induced inflammation, calcification, vascular smooth muscle cell stiffness, and endothelial dysfunction. This brief review will discuss current biological mechanisms by which other cardiovascular risk factors (eg, aging, hypertension, diabetes mellitus, and chronic kidney disease) cause arterial stiffness, with a particular focus on recent advances regarding nuclear mechanotransduction, mitochondrial oxidative stress, metabolism and dyslipidemia, genome mutations, and epigenetics. Targeting these different molecular pathways at different time of cardiovascular risk factor exposure may be a novel approach for discovering drugs to reduce arterial stiffening without affecting artery strength and normal remodeling.
引用
收藏
页码:1055 / 1062
页数:8
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