Xanthine oxidoreductase in atherosclerosis pathogenesis: Not only oxidative stress

被引:194
作者
Battelli, Maria Giulia [1 ]
Polito, Letizia [1 ]
Bolognesi, Andrea [1 ]
机构
[1] Alma Mater Studiorum Univ Bologna, Dept Expt Diagnost & Specialty Med DIMES, Gen Pathol Unit, I-40126 Bologna, Italy
关键词
Atherosclerosis; Cardiovascular diseases; Metabolic syndrome; Oxidative stress; Uric acid; Xanthine oxidoreductase; OXIDASE INHIBITOR FEBUXOSTAT; FREE-RADICAL PRODUCTION; URIC-ACID; ENDOTHELIAL DYSFUNCTION; NAD(P)H OXIDASE; CARDIOVASCULAR-DISEASE; HYPERTENSION; HYPERURICEMIA; DEHYDROGENASE; PROTECTION;
D O I
10.1016/j.atherosclerosis.2014.10.006
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Endothelial xanthine oxidoreductase (XOR) together with NAD(P) H oxidase and nitric oxide (NO) synthase plays a physiologic role in inflammatory signalling, the regulation of NO production and vascular function. The oxidative stress generated by these enzymes may induce endothelial dysfunction, leading to atherosclerosis, cardiovascular diseases and metabolic syndrome. XOR activity creates both oxidant and anti-oxidant products that are implicated in the development of hypertension, smoking vascular injury, dyslipidemia and diabetes, which are the main risk factors of atherosclerosis. In particular, uric acid may have a protective as well as a detrimental role in vascular alterations, thus justifying the multidirectional effects of XOR inhibition. Moreover, XOR products are associated with cell differentiation, leading to adipogenesis and foam cell formation, as well as to the production of monocyte chemoattractant protein-1 from arterial smooth muscle cells, after proliferation and migration. The role of XOR in adipogenesis is also connected with insulin resistance and obesity, two main features of type 2 diabetes. (C) 2014 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:562 / 567
页数:6
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