Oxidative damage of albumin in advanced liver disease

被引:119
作者
Oettl, Karl [1 ]
Stadlbauer, Vanessa [2 ]
Petter, Franz [1 ]
Greilberger, Joachim [1 ]
Putz-Bankuti, Csilla [2 ]
Hallstroem, Seth [1 ]
Lackner, Carolin [3 ]
Stauber, Rudolf E. [2 ]
机构
[1] Med Univ Graz, Ctr Physiol Med, Inst Physiol Chem, A-8010 Graz, Austria
[2] Med Univ Graz, Dept Internal Med, Div Gastroenterol & Hepatol, A-8010 Graz, Austria
[3] Med Univ Graz, Inst Pathol, A-8010 Graz, Austria
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2008年 / 1782卷 / 7-8期
关键词
oxidative stress; acute-on-chronic liver failure; liver cirrhosis; mercaptalbumin; bilirubin binding;
D O I
10.1016/j.bbadis.2008.04.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Albumin has a number of biological functions and the serum albumin level is related to prognosis in advanced liver disease. Oxidative stress is believed to play an important role in the pathogenesis of liver failure. The aim of the present study was to characterize oxidative modification of albumin in patients with various degrees of liver failure and to investigate implications for its binding function. Patients with liver cirrhosis (n = 10), acute-on-chronic liver failure (n = 8) and healthy controls (n = 15) were included in the study. Three fractions of albumin were separated by HPLC according to the redox state of cysteine-34 and detected by fluorescence as well as UV absorption. Carbonyl groups were measured as a marker of oxidative modification in plasma proteins and, by western blotting, on albumin. Progressive oxidative modification of albumin was found with increasing severity of liver failure indicated by an increased content of carbonyl groups and oxidation of cysteine-34. Fluorescence properties of albumin were altered by oxidation and, in patients with acute-on-chronic liver failure, by high plasma levels of bilirubin. This alteration of albumin fluorescence by bilirubin provides evidence for a preferred binding of bilirubin to the fully reduced form of albumin. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:469 / 473
页数:5
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