Intravenous iron administration induces oxidation of serum albumin in hemodialysis patients

被引:91
作者
Anraku, M
Kitamura, K
Shinohara, A
Adachi, M
Suenaga, A
Maruyama, T
Miyanaka, K
Miyoshi, T
Shiraishi, N
Nonoguchi, H
Otagiri, M
Tomita, K
机构
[1] Kumamoto Univ, Grad Sch Med Sci, Fac Med & Pharmaceut Sci, Dept Nephrol, Kumamoto 8608556, Japan
[2] Kumamoto Univ, Fac Med & Pharmaceut Sci, Dept Biopharmaceut, Kumamoto 8608556, Japan
关键词
albumin; oxidative stress; hemodialysis; saccharated ferric oxide;
D O I
10.1111/j.1523-1755.2004.00813.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Intravenous iron administration (IVIR) is effective for correcting anemia in hemodialysis (HD) patients. However, it may also enhance the generation of hydroxyl radicals. Recently, plasma proteins have been demonstrated to be extremely susceptible to oxidative stress. Therefore, we investigated the effect of IVIR on the oxidative status of albumin, a major plasma protein, in HD patients. Methods. Eleven hemodialysis (HD) patients were treated with 40 mg of saccharated ferric oxide intravenously after every dialysis session for four weeks, and 11 age-/gender-matched HD patients were treated with vehicle. We performed high performance liquid chromatography (HPLC) analysis of serum albumin and determined the levels of reduced and oxidized albumin. Carbonyl formation of plasma proteins were also measured using an anti-2,4 dinitrophenylhydrazine antibody in patients with or without IVIR. Results. IVIR resulted in an increase in both disulfide form (f( HNA-1)) and oxidized form (f(HNA-2)) of albumin in HD patients (36.0 +/- 6.03 vs. 41.7 +/- 6.27; 5.46 +/- 1.50 vs. 8.7 +/- 2.22, respectively, P < 0.05). The findings here also show that IVIR substantially increased plasma protein carbonyl content by oxidizing albumin. In addition, we found a strong correlation between plasma carbonyl content and the levels of oxidized albumin (f( HNA-1) and f( HNA-2)) in HD patients (R = 0.674 and R = 0.724, respectively, P < 0.01). Conclusion. The results of this study indicate that the HPLC analysis of serum albumin represents a potentially useful method for the quantitative and qualitative evaluation of oxidative stress in HD patients, and strongly suggest the possibility that oxidative stress, generated by IVIR, enhances the oxidation of albumin in those patients.
引用
收藏
页码:841 / 848
页数:8
相关论文
共 42 条
[1]   Validation of the chloramine-T induced oxidation of human serum albumin as a model for oxidative damage in vivo [J].
Anraku, M ;
Kragh-Hansen, U ;
Kawai, K ;
Maruyama, T ;
Yamasaki, Y ;
Takakura, Y ;
Otagiri, M .
PHARMACEUTICAL RESEARCH, 2003, 20 (04) :684-692
[2]   A biochemical, histochemical, and electron microscopic study on the effects of iron-loading on the hearts of mice [J].
Bartfay, WJ ;
Butany, J ;
Lehotay, DC ;
Sole, MJ ;
Hou, D ;
Bartfay, E ;
Liu, PP .
CARDIOVASCULAR PATHOLOGY, 1999, 8 (06) :305-314
[3]   Protein oxidation in aging, disease, and oxidative stress [J].
Berlett, BS ;
Stadtman, ER .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20313-20316
[4]   Secondary prevention with antioxidants of cardiovascular disease in endstage renal disease (SPACE): randomised placebo-controlled trial [J].
Boaz, M ;
Smetana, S ;
Weinstein, T ;
Matas, Z ;
Gafter, U ;
Iaina, A ;
Knecht, A ;
Weissgarten, Y ;
Brunner, D ;
Fainaru, M ;
Green, MS .
LANCET, 2000, 356 (9237) :1213-1218
[5]   DERIVATIZATION OF GAMMA-GLUTAMYL-TRANSFERASE SEMIALDEHYDE RESIDUES IN OXIDIZED PROTEINS BY FLUORESCEINAMINE [J].
CLIMENT, I ;
TSAI, L ;
LEVINE, RL .
ANALYTICAL BIOCHEMISTRY, 1989, 182 (02) :226-232
[6]   Influence of dialysis on plasma lipid peroxidation products and antioxidant levels [J].
Daschner, M ;
Lenhartz, H ;
Botticher, D ;
Schaefer, F ;
Wollschlager, M ;
Mehls, O ;
Leichsenring, M .
KIDNEY INTERNATIONAL, 1996, 50 (04) :1268-1272
[7]  
Dean RT, 1997, BIOCHEM J, V324, P1
[8]   REACTION OF NITRIC-OXIDE WITH THE FREE SULFHYDRYL-GROUP OF HUMAN SERUM-ALBUMIN YIELDS A SULFENIC ACID AND NITROUS-OXIDE [J].
DEMASTER, EG ;
QUAST, BJ ;
REDFERN, B ;
NAGASAWA, HT .
BIOCHEMISTRY, 1995, 34 (36) :11494-11499
[9]  
Descamps-Latscha B, 2001, KIDNEY INT, V59, pS108
[10]   Iron therapy, advanced oxidation protein products, and carotid artery intima-media thickness in end-stage renal disease [J].
Drüeke, T ;
Witko-Sarsat, V ;
Massy, Z ;
Descamps-Latscha, B ;
Guerin, AP ;
Marchais, SJ ;
Gausson, V ;
London, GM .
CIRCULATION, 2002, 106 (17) :2212-2217