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Correlation of changes in nitric oxide synthase, superoxide dismutase and nitrotyrosine with endothelial regeneration and neointimal hyperplasia in the balloon-injured rabbit subclavian artery
被引:9
作者:
Kennedy, S
Preston, AA
McPhaden, AR
Miller, AM
Wainwright, CL
Wadsworth, RM
机构:
[1] Univ Strathclyde, Strathcycle Inst Biol Sci, Dept Physiol & Pharmacol, Glasgow G4 0NR, Lanark, Scotland
[2] Glasgow Royal Infirm, Dept Pathol, Glasgow G4 0SF, Lanark, Scotland
关键词:
vascular injury;
nitric oxide synthase;
superoxide dismutase;
nitrotyrosine;
D O I:
10.1097/00019501-200409000-00007
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives Alterations in nitric oxide (NO) and superoxide production within the wall of injured vessels may modulate the development and eventual extent of neointima after balloon injury. Methods In this study we have characterized a rabbit model of subclavian artery injury and have used immunocytochemistry to detect NO synthase (NOS) isoforms, Cu-Zn superoxide dismutase (SOD) and nitrotyrosine in the injured vessel from 2 h to 28 days after injury. Results At 48 h after injury, when cellular proliferation that will ultimately form the neointima is commencing, there was upregulation of inducible NOS, Cu-Zn SOD and nitrotyrosine. Recovery of endothelial NOS occurred at 28 days after injury, when the neointima is stabilizing and cellular proliferation has slowed down. There was no increase in neuronal NOS at any time point studied. Conclusions NO may serve to limit the development of neointima while superoxide may attenuate the effect of NO by formation of peroxynitrite, detected as increased nitrotyrosine staining. Upregulation of Cu-Zn SOD would limit superoxide both at sites of inflammation in the vessel wall from 48 h and in the adventitia up to 28 days after injury. Very early intervention to protect NO may reduce neointimal size. (C) 2004 Lippincott Williams Wilkins.
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页码:337 / 346
页数:10
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