Oxidative Stress in Vivax Malaria

被引:24
作者
Bilgin, Ramazan [1 ]
Yalcin, Mustafa S. [1 ]
Yucebilgic, Guzide [1 ]
Koltas, Ismail S. [2 ]
Yazar, Suleyman [3 ]
机构
[1] Cukurova Univ, Arts & Sci Fac, Dept Chem, Div Biochem, Adana, Turkey
[2] Cukurova Univ, Fac Med, Dept Parasitol, Adana, Turkey
[3] Erciyes Univ, Fac Med, Dept Parasitol, Kayseri, Turkey
关键词
Plasmodium vivax; malondialdehyde; superoxide dismutase; glutathione peroxidase; malaria; ACUTE FALCIPARUM-MALARIA; PLASMODIUM-VIVAX; LIPID-PEROXIDATION; MALONDIALDEHYDE; ERYTHROCYTES; GLUTATHIONE; BLOOD; ASSAY;
D O I
10.3347/kjp.2012.50.4.375
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Malaria is still a leading cause of morbidity and mortality. The increase in lipid peroxidation reported in malaria infection and antioxidant status may be a useful marker of oxidative stress during malaria infection. The aim of this study was to investigate the role of antioxidant enzymes against toxic reactive oxygen species in patients infected with Plasmodium vivax and healthy controls. Malondialdehyde levels, superoxide dismutase, and glutathione peroxidase activities were determined in 91 P vivax patients and compared with 52 controls. Malondialdehyde levels, superoxide dismutase, and glutathione peroxidase activities were 8.07 +/- 2.29 nM/ml, 2.69 +/- 0.33 U/ml, and 49.6 +/- 3.2 U/g Hb in the patient group and 2.72 +/- 0.50 nM/ml, 3.71 +/- 0.47 U/ml, and 62.3 +/- 4.3 U/g Hb in the control group, respectively. Malondialdehyde levels were found statistically significant in patients with vivax malaria higher than in healthy controls (P<0.001). On the other hand, superoxide dismutase and glutathione peroxidase activities were found to be significantly lower in vivax malaria patients than in controls (P<0.05). There was an increase in oxidative stress in vivax malaria. The results suggested that antioxidant defense mechanisms may play an important role in the pathogenesis of P vivax.
引用
收藏
页码:375 / 377
页数:3
相关论文
共 25 条
[1]  
Akdur R, 2004, SITMA TEMEL BILGILER, P1
[2]   Oxidative stress in malaria parasite-infected erythrocytes: host-parasite interactions [J].
Becker, K ;
Tilley, L ;
Vennerstrom, JL ;
Roberts, D ;
Rogerson, S ;
Ginsburg, H .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2004, 34 (02) :163-189
[3]  
Beutler E., 1975, RED CELL METABOLISM, P74
[4]   REDUCTION IN ERYTHROCYTIC GSH LEVEL AND STABILITY IN PLASMODIUM-VIVAX MALARIA [J].
BHATTACHARYA, J ;
SWARUPMITRA, S .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1987, 81 (01) :64-66
[5]   INACTIVATION OF GLUTATHIONE-PEROXIDASE BY SUPEROXIDE RADICAL [J].
BLUM, J ;
FRIDOVICH, I .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 240 (02) :500-508
[6]   Evidence for erythrocyte lipid peroxidation in acute falciparum malaria [J].
Das, BS ;
Nanda, NK .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1999, 93 (01) :58-62
[7]   GENERATION OF REACTIVE OXYGEN SPECIES IN WHOLE-BLOOD FROM PATIENTS WITH ACUTE FALCIPARUM-MALARIA [J].
DESCAMPSLATSCHA, B ;
LUNELFABIANI, F ;
KARABINIS, A ;
DRUILHE, P .
PARASITE IMMUNOLOGY, 1987, 9 (02) :275-279
[8]   A REVIEW OF RECENT STUDIES ON THE METABOLISM OF EXOGENOUS AND ENDOGENOUS MALONDIALDEHYDE [J].
DRAPER, HH ;
HADLEY, M .
XENOBIOTICA, 1990, 20 (09) :901-907
[9]   Oxidative stress and antioxidative status of plasma and erythrocytes in patients with vivax malaria [J].
Erel, O ;
Kocyigit, A ;
Avci, S ;
Aktepe, N ;
Bulut, V .
CLINICAL BIOCHEMISTRY, 1997, 30 (08) :631-639
[10]   Nonoperative treatment of splenic rupture in malaria tropica: review of literature and case report [J].
Hamel, CT ;
Blum, J ;
Harder, F ;
Kocher, T .
ACTA TROPICA, 2002, 82 (01) :1-5