Role of oxidative stress in atherosclerosis

被引:32
|
作者
Harrison, D
Griendling, KK
Landmesser, U
Hornig, B
Drexler, H
机构
[1] Emory Univ, Sch Med, Div Cardiol, Dept Med, Atlanta, GA 30322 USA
[2] Hannover Med Sch, Dept Cardiol & Angiol, Hannover, Germany
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2003年 / 91卷 / 03期
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The common risk factors for atherosclerosis increase production of reactive oxygen species (ROS) by endothelial, vascular smooth muscle, and adventitial cells. These ROS initiate processes involved in atherogenesis through several important enzyme systems, including xanthine oxidase, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and nitric oxide synthase. also regulate vascular production of ROS. Oscillatory shear, which is present at sites where atherosclerosis develops, seems a particularly potent stimulus of superoxide production. The signaling cascade for activation of the NAD(P)H oxidase by angiotensin II has recently been elucidated and seems to involve a feed-forward mechanism that permits ongoing production of ROS for prolonged periods. Oxidative stress in humans with coronary artery disease is also exacerbated by a reduction of vascular extracellular superoxide dismutase, normally an important protective enzyme against the superoxide anion. (C) 2003 by Excerpta Medica, Inc.
引用
收藏
页码:7A / 11A
页数:5
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