Oxidative stress and abdominal aortic aneurysm: potential treatment targets

被引:102
作者
Emeto, Theophilus I. [1 ,2 ]
Moxon, Joseph V. [1 ]
Au, Minnie [2 ,3 ]
Golledge, Jonathan [1 ,4 ]
机构
[1] James Cook Univ, Coll Med & Dent, Queensland Res Ctr Peripheral Vasc Dis, Vasc Biol Unit, Townsville, Qld 4811, Australia
[2] James Cook Univ, Coll Publ Hlth Med & Vet Studies, Discipline Publ Hlth & Trop Med, Townsville, Qld 4811, Australia
[3] Townsville Hosp, Dept Internal Med, Townsville, Qld 4814, Australia
[4] Townsville Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld 4814, Australia
基金
英国医学研究理事会;
关键词
abdominal aortic aneurysm; animal models; clinical trial; oxidative stress; pharmacotherapy; NITRIC-OXIDE SYNTHASE; EXTRACELLULAR-SUPEROXIDE DISMUTASE; OXYGENASE-1 GENE PROMOTER; NF-KAPPA-B; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PROSTAGLANDIN E-2 SYNTHESIS; HIGH-DENSITY-LIPOPROTEIN; FREE-RADICAL SCAVENGER; SMOOTH-MUSCLE-CELLS; ANGIOTENSIN-II;
D O I
10.1042/CS20150547
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Abdominal aortic aneurysm (AAA) is a significant cause of mortality in older adults. A key mechanism implicated in AAA pathogenesis is inflammation and the associated production of reactive oxygen species (ROS) and oxidative stress. These have been suggested to promote degradation of the extracellular matrix (ECM) and vascular smooth muscle apoptosis. Experimental and human association studies suggest that ROS can be favourably modified to limit AAA formation and progression. In the present review, we discuss mechanisms potentially linking ROS to AAA pathogenesis and highlight potential treatment strategies targeting ROS. Currently, none of these strategies has been shown to be effective in clinical practice.
引用
收藏
页码:301 / 315
页数:15
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