t-BOOH-induced oxidative damage in sickle red blood cells and the role of flavonoids

被引:71
作者
Cesquini, M [1 ]
Torsoni, MA
Stoppa, GR
Ogo, SH
机构
[1] Univ Estadual Campinas, Dept Bioquim, Inst Biol, BR-13083970 Campinas, SP, Brazil
[2] Univ Braz Cubas, Mogi Daz Cruzes, SP, Brazil
关键词
sickle cell anemia; flavonoids; RBC oxidation;
D O I
10.1016/S0753-3322(03)00018-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Sickle cell anemia is a genetic disease characterized by an increase in generation of reactive oxygen species, abnormal iron release and low antioxidant activity which can lead to cell injury. Several therapies have been used to decrease the oxidative damage in these patients. In this study, we investigated the effect of flavonoids (quercetin and rutin) on the oxidation of red blood cells (RBC) from sickle cell anemia patients following exposure of the cells to tert-butyl hydroperoxide (t-BOOH). Quercetin provided greater protection against Hb oxidation, the binding of Hb to membrane and lipid peroxidation than did rutin. Quercetin (150 muM) reduced Hb oxidation by 30% and increased the level of oxyHb from 17.5 to 29 muM. Rutin prevented Hb oxidation only at concentrations higher than 200 muM and did not prevent the binding of Hb to RBC membrane. These distinct effects of the flavonoids probably reflect their structural characteristics. Thus, quercetin, which possesses a suitable structure for free-radical scavenging and ion quelation, was a more effective antioxidant than rutin. The presence of rutinose at position C-3 in rutin may impair its antioxidant effect. The presence of ascorbic acid enhanced the protective effect of quercetin and rutin against oxidative stress in sickle Hb and lipid peroxidation. This synergistic action helped to maintain a constant supply of flavonoids and thus, rescue the cells from the injury caused by free radicals and iron ions. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:124 / 129
页数:6
相关论文
共 42 条
[1]
Adachi Kazuhiko, 1994, P99
[2]
CHELATING AND FREE-RADICAL SCAVENGING MECHANISMS OF INHIBITORY-ACTION OF RUTIN AND QUERCETIN IN LIPID-PEROXIDATION [J].
AFANASEV, IB ;
DOROZHKO, AI ;
BRODSKII, AV ;
KOSTYUK, VA ;
POTAPOVITCH, AI .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (11) :1763-1769
[3]
INTERACTION OF FLAVONOIDS WITH ASCORBATE AND DETERMINATION OF THEIR UNIVALENT REDOX POTENTIALS - A PULSE-RADIOLYSIS STUDY [J].
BORS, W ;
MICHEL, C ;
SCHIKORA, S .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (01) :45-52
[4]
BORS W, 1994, METHOD ENZYMOL, V234, P420
[5]
BORS W, 1990, METHOD ENZYMOL, V186, P343
[6]
FLAVONOIDS - BIOCHEMICAL EFFECTS AND THERAPEUTIC APPLICATIONS [J].
BRANDI, ML .
BONE AND MINERAL, 1992, 19 :S3-S14
[7]
The molecular pathobiology of cell membrane iron: The sickle red cell as a model [J].
Browne, P ;
Shalev, O ;
Hebbel, RP .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (06) :1040-1048
[8]
BIOCHEMISTRY OF OXYGEN-TOXICITY [J].
CADENAS, E .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :79-110
[9]
Quercetin diminishes the binding of hemoglobin to the red blood cell membrane [J].
Cesquini, M ;
Tenor, AC ;
Torsoni, MA ;
Stoppa, GR ;
Pereira, AL ;
Ogo, SH .
JOURNAL OF ANTI-AGING MEDICINE, 2001, 4 (01) :55-63
[10]
Correlation of membrane lipid peroxidation with oxidation of hemoglobin variants: Possibly related to the rates of hemin release [J].
Chiu, DTY ;
VanDenBerg, J ;
Kuypers, FA ;
Hung, IJ ;
Wei, JS ;
Liu, TZ .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (01) :89-95