Heme oxygenase-1 levels and oxidative stress-related parameters in non-alcoholic fatty liver disease patients

被引:164
作者
Malaguarnera, L
Madeddu, R
Palio, E
Arena, N
Malaguarnera, M
机构
[1] Univ Catania, Dept Biomed Sci, I-95039 Trecastagni Catan, Italy
[2] Univ Catania, Dept Senescence Urol & Neurol Sci, I-95124 Catania, Italy
[3] Univ Sassari, Dept Biomed Sci, I-07100 Sassari, Italy
关键词
non-alcoholic steatohepatitis; simple steatosis; heme oxygenase-1; ferritin; lipid peroxidation; GSH;
D O I
10.1016/j.jhep.2004.11.040
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Non-alcoholic steatohepatitis (NASH) is a disorder that is histologically characterized by macrovesicular steatosis and lobular hepatitis with necrosis or ballooning degeneration and fibrosis. NASH can range from a benign condition to end-stage liver disease. The mechanisms promoting transition from steatosis to NASH appear to involve multiple cellular adaptations to the oxidative stress occurring when fatty acid metabolism is altered. We evaluated the relationship between lipid peroxidation and other oxidative stress biomarkers with changes in expression of heme oxygenase-1 (HO-1) in human hepatic steatosis ranging from simple steatosis to NASH. Methods: HO-1 expression, lipid peroxidation, ferritin and GSH levels were assayed from liver biopsies obtained from 60 subjects: 35 with NASH, 15 with simple steatosis and 10 controls. Results: The HO-1 expression was significantly increased in NASH patients and the increase reflected the severity of the disease. A significant correlation was observed between the increased levels of HO-1 and ferritin, and between the increased levels of HO-1 and lipid peroxidation. Moreover, NASH patients with lower levels of GSH exhibited higher expression of HO-1. Conclusions: The induction of HO-1 is an adaptive response against oxidative damage elicited by lipid peroxidation and it may be critical in the progression of the disease. (C) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:585 / 591
页数:7
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