Effects of long term ethanol consumption mediated oxidative stress on neovessel generation in liver

被引:12
作者
Das, Subir Kumar [1 ,2 ]
Mukherjee, Sukhes [3 ]
Vasudevan, D. M. [3 ]
机构
[1] WBUHS, Coll Med, Dept Biochem, Kalyani, Nadia, India
[2] WBUHS, JNM Hosp, Kalyani, Nadia, India
[3] Amrita Inst Med Sci, Dept Biochem, Cochin, Kerala, India
关键词
Ethanol; matrix metalloproteinases; oxidative stress; vascular endothelial growth factor-receptor; von Willebrand factor; ENDOTHELIAL GROWTH-FACTOR; VON-WILLEBRAND-FACTOR; GLUTATHIONE PEROXIDASE; ANGIOGENESIS; DISEASE; EXPRESSION; ALCOHOL; VEGF; ADHESION; CELLS;
D O I
10.3109/15376516.2012.666651
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
Angiogenesis, the growth of new blood vessels, is essential during tissue repair. Though most molecular mechanisms of angiogenesis are common to the liver and other organs, there was no report available whether alcoholic liver disease also causes angiogenesis. In this study, we examined the effects of long term ethanol (1.6 g/kg body weight/day) consumption on angiogenic responses in the liver of male Wistar strain albino rats (16-18 weeks old, weighing 200-220 g) up to 36 weeks. Chronic ethanol consumption was associated with not only elevated oxidative stress, and altered cytokines expression, but also developed large von Willebrand factor, fibrosis and activation of matrix metalloproteinases. Moreover, vascular endothelial growth factor-receptor 2 (VEGF-R2, fetal liver kinase 1: Flk-1/KDR) expression and neovessel generation in the rat liver were noted after 36 weeks of ethanol consumption. Thus our study provides novel evidence that long-term ethanol consumption is associated with angiogenesis through delicate and coordinated action of a variety of mediators.
引用
收藏
页码:375 / 382
页数:8
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