The Frail Renin-Angiotensin System

被引:56
作者
Abadir, Peter M. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Geriatr Med & Gerontol, Baltimore, MD 21224 USA
关键词
Renin-angiotensin system; Cardiovascular disease; Apoptosis; AT1R; Oxidative stress; AT2R; Inflammation; VASCULAR SMOOTH-MUSCLE; END-POINT REDUCTION; NECROSIS-FACTOR-ALPHA; INTERLEUKIN-6; GENE-EXPRESSION; LEFT-VENTRICULAR HYPERTROPHY; ONSET ATRIAL-FIBRILLATION; II RECEPTOR BLOCKADE; TYPE-2; RECEPTOR; LOSARTAN INTERVENTION; AT(2) RECEPTORS;
D O I
10.1016/j.cger.2010.08.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Over the last few decades, the understanding of the renin-angiotensin system (RAS) has advanced dramatically. RAS is now thought to play a crucial role in physiologic and pathophysiologic mechanisms in almost every organ system and is a key regulator of hypertension, cardiovascular disease, and renal function. Angiotensin II (Ang II) promotes inflammation and the generation of reactive oxygen species and governs onset and progression of vascular senescence, which are all associated with functional and structural changes, contributing to age-related diseases. Although the vast majority of the actions of Ang II, including vascular senescence, are mediated by the Ang II type 1 receptor (AT1R), the identification, characterization, and cloning of the angiotensin type 2 receptor has focused attention on this receptor and to its antagonistic effect on the detrimental effects of AT1 R. This review provides an overview of the changes in RAS with aging and age-disease interactions culminating in the development of frailty.
引用
收藏
页码:53 / +
页数:14
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