Reduced serum hydroxyl radical scavenging activity in erythropoietin therapy resistant renal anemia

被引:20
作者
Hirayama, A
Nagase, S
Gotoh, M
Ueda, A
Ishizu, T
Yoh, K
Aoyagi, K
Terao, J
Koyama, A
机构
[1] Univ Tsukuba, Inst Clin Med, Dept Internal Med, Tsukuba, Ibaraki 3058575, Japan
[2] Tsukuba Coll Technol, Tsukuba, Ibaraki, Japan
[3] Tsukuba Cent Hosp, Dialysis Ctr, Ushiku, Japan
[4] Hitachi Gen Hosp, Dept Nephrol, Hitachi, Ibaraki, Japan
[5] Univ Tokushima, Sch Med, Tokushima 770, Japan
基金
日本学术振兴会;
关键词
hemodialysis; lipid peroxidation; hydroxyl radical; erythropoietin; renal anemia;
D O I
10.1080/1071576021000016418
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
Relation between anemia resistant to recombinant human erythropoietin (rHuEPO) therapy and the oxidative stress in hemodialysis (HD) patients was investigated. Stable HD patients who had consistent hemoglobin concentrations on a constant dose of rHuEPO were studied. Patients were excluded if there were factors that might affect hemopoiesis or administration of antioxidant supplements. Patients were classified into three groups: High (9000U/week), Low (1500 -4500 U /week) and No rHuEPO group. Thiobarbituric acid reactive substances (TBARS) of sera and erythrocyte were examined. Serum superoxide and hydroxyl radical scavenging activities were measured using electron spin resonance. TBARS in the erythrocyte was higher in High rHuEPO group compared with No rHuEPO group, though the serum TBARS were similar. A diminution of serum hydroxyl radical scavenging activity was observed in High rHuEPO group. Hydroxyl radical signal intensity showed a strong correlation with the serum ferritin in High rHuEPO group, although ferritin concentrations were not different among the 3 groups. Superoxide scavenging activity showed no differences. These results indicate that increased lipid peroxidation in erythrocyte, raised by decreased serum hydroxyl radical scavenging activity, is one cause of rHuEPO resistant anemia. Serum ferritin may be involved in this hydroxyl radical production.
引用
收藏
页码:1155 / 1161
页数:7
相关论文
共 18 条
  • [1] Besarab A, 2000, J AM SOC NEPHROL, V11, P530, DOI 10.1681/ASN.V113530
  • [2] Serum malondialdehyde and prevalent cardiovascular disease in hemodialysis
    Boaz, M
    Matas, Z
    Biro, A
    Katzir, Z
    Green, M
    Fainaru, M
    Smetana, S
    [J]. KIDNEY INTERNATIONAL, 1999, 56 (03) : 1078 - 1083
  • [3] Secondary prevention with antioxidants of cardiovascular disease in endstage renal disease (SPACE): randomised placebo-controlled trial
    Boaz, M
    Smetana, S
    Weinstein, T
    Matas, Z
    Gafter, U
    Iaina, A
    Knecht, A
    Weissgarten, Y
    Brunner, D
    Fainaru, M
    Green, MS
    [J]. LANCET, 2000, 356 (9237) : 1213 - 1218
  • [4] The molecular pathobiology of cell membrane iron: The sickle red cell as a model
    Browne, P
    Shalev, O
    Hebbel, RP
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (06) : 1040 - 1048
  • [5] EVANS RW, 1990, JAMA-J AM MED ASSOC, V263, P825
  • [6] Gallucci MT, 1999, CLIN NEPHROL, V52, P239
  • [7] Thiobarbituric acid reactive substances are increased in the subcutaneous fat tissue of patients with end-stage renal disease
    Gotoh, M
    Nagase, S
    Aoyagi, K
    Hirayama, A
    Takemura, K
    Ueda, A
    Tomida, C
    Kikuchi, H
    Koyama, A
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 1997, 12 (04) : 713 - 717
  • [8] Hemodialysis does not influence the peroxidative state already present in uremia
    Hirayama, A
    Nagase, S
    Gotoh, M
    Takemura, K
    Tomida, C
    Ueda, A
    Aoyagi, K
    Terao, J
    Koyama, A
    [J]. NEPHRON, 2000, 86 (04): : 436 - 440
  • [9] MACDOUGALL IC, 1995, NEPHROL DIAL TRANSPL, V10, P607
  • [10] Nagase S, 1997, J AM SOC NEPHROL, V8, P1157