Increased DNA damage and oxidative stress in patients with cutaneous leishmaniasis

被引:113
作者
Kocyigit, A [1 ]
Keles, H [1 ]
Selek, S [1 ]
Guzel, S [1 ]
Celik, H [1 ]
Erel, O [1 ]
机构
[1] Harran Univ, Fac Med, Dept Biochem, TR-63200 Sanliurfa, Turkey
关键词
cutaneous leishmaniasis; DNA damage; oxidative status; total anti-oxidative response;
D O I
10.1016/j.mrgentox.2005.04.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cutaneous leishmaniasis (CL) is a chronic infectious and granulomatous disease caused by the Leishmania parasite that invades the skin. Reactive oxygen and nitrogen species (ROS and RNS) produced during an inflammatory response are an important part of host-defense strategies of organisms to kill the parasite. However, it is not well known whether these intermediates cause DNA damage in CL patients. We investigated the effect of Leishmania infection on basal levels of DNA strand breaks and on the oxidative/anti-oxidative status of patients with CL, and compared the data with those of healthy subjects. Twenty-five CL patients and 19 age- and sex-matched control subjects were enrolled in the study. We used the single-cell gel electrophoresis (also called comet assay) to measure DNA strand breaks in peripheral blood mononuclear leukocytes. Plasma protein carbonyl (PC), malondialdehyde (MDA) and total peroxide (TP) concentrations were measured to determine oxidative status and total anti-oxidative response (TAR) in plasma was measured to determine anti-oxidative status. The mean values of DNA damage and MDA and TP concentrations were significantly higher in CL patients than in the control group (p < 0.001, p < 0.01 and p < 0.001, respectively). PC levels were also higher in patients, but this was not statistically significant (p > 0.05). There was a significantly positive correlation between plasma MDA and DNA damage (r = 0.524, p < 0.01), and a negative correlation between TAR and TP levels (r = -0.790, p < 0.001) in the patient group. These findings support the notion that ROS and RNS produced by the organism as a defense strategy may amplify the leishmanicidal activity in patients with CL. However, these intermediates not only cause the killing of the parasite but also induce oxidative damage in non-infected cells. Therefore, these patients must be treated urgently to counteract the oxidative DNA damage. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
相关论文
共 41 条
  • [1] THE CAUSES AND PREVENTION OF CANCER
    AMES, BN
    GOLD, LS
    WILLETT, WC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) : 5258 - 5265
  • [2] Beckman JS, 1996, AM J PHYSIOL-CELL PH, V271, pC1424
  • [3] The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay
    Benzie, IFF
    Strain, JJ
    [J]. ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) : 70 - 76
  • [4] A tale of two controversies -: Defining both the role of peroxidases in nitrotyrosine formation in vivo using eosinophil peroxidase and myeloperoxidase-deficient mice, and the nature of peroxidase-generated reactive nitrogen species
    Brennan, ML
    Wu, WJ
    Fu, XM
    Shen, ZZ
    Song, W
    Frost, H
    Vadseth, C
    Narine, L
    Lenkiewicz, E
    Borchers, MT
    Lusis, AJ
    Lee, JJ
    Lee, NA
    Abu-Soud, HM
    Ischiropoulos, H
    Hazen, SL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (20) : 17415 - 17427
  • [5] SOMATIC MUTANT FREQUENCY, MUTATION-RATES AND MUTATIONAL SPECTRA IN THE HUMAN-POPULATION IN-VIVO
    COLE, J
    SKOPEK, TR
    [J]. MUTATION RESEARCH, 1994, 304 (01): : 33 - 105
  • [6] CONTI M, 1991, CLIN CHEM, V37, P1273
  • [7] Relationship between DNA damage, total antioxidant capacity and coronary artery disease
    Demirbag, R
    Yimaz, R
    Kocyigit, A
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 570 (02) : 197 - 203
  • [8] DNA damage and antioxidant defense in peripheral leukocytes of patients with type I diabetes mellitus
    Dinçer, Y
    Akçay, T
    Ilkova, H
    Alademir, Z
    Özbay, G
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 527 (1-2) : 49 - 55
  • [9] DIZDAROGLU M, 1994, METHOD ENZYMOL, V234, P3
  • [10] Reactive nitrogen and oxygen intermediates in patients with cutaneous leishmaniasis
    Erel, O
    Kocyigit, A
    Bulut, V
    Gurel, MS
    [J]. MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1999, 94 (02): : 179 - 183