Protective effect of hydrogen sulfide on balloon injury-induced neointima hyperplasia in rat carotid arteries

被引:122
作者
Meng, Qing H.
Yang, Guangdong
Yang, Wei
Jiang, Bo
Wu, Lingyun
Wang, Rui
机构
[1] Lakehead Univ, Dept Biol, Thunder Bay, ON P7B 5E1, Canada
[2] Univ Saskatchewan, Dept Pathol & Lab Med, Saskatoon, SK, Canada
[3] Univ Saskatchewan, Dept Physiol, Saskatoon, SK, Canada
[4] Univ Saskatchewan, Dept Pharmacol, Saskatoon, SK S7N 0W0, Canada
基金
加拿大健康研究院;
关键词
D O I
10.2353/ajpath.2007.060939
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Endogenous hydrogen sulfide (H2S), generated from homocysteine metabolism mainly catalyzed by cystathionine gamma-lyase (CSE), possesses important functions in the cardiovascular system. in this study, we investigated the role of H,S during the pathogenesis of neointimal formation induced by balloon injury in rats. CSE mRNA levels were reduced by 86.5% at 1 week and 64.0% at 4 weeks after balloon injury compared with the uninjured controls. CSE activity was also correspondingly reduced. Endogenous production of H,S in the injured carotid artery was significantly inhibited at 1 week and 4 weeks after balloon injury. Treatment with NaHS (a donor of H,S) enhanced methacholine-induced vasorelaxation of balloon-injured artery. More importantly, treatment with NaHs significantly inhibited neointima formation (0.15 +/- 0.01 nun 2 versus 0.21 +/- 0.01 mm(2), P < 0.001) of the balloon-injured carotid arteries and reduced the intima/media ratio (1.05 +/- 0.07 versus 1.43 +/- 0.06, P < 0.001). A significant decrease in vascular smooth muscle cell proliferation was demonstrated by bromodeoxyuridine incorporation at day 7 after injury. In conclusion, CSE expression and H,S production are reduced during the development of balloon injury-induced neointimal hyperplasia, and treatment with NaHS significantly reduces neointimal lesion formation.
引用
收藏
页码:1406 / 1414
页数:9
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