Supplementation with antioxidant vitamins prevents oxidative modification of DNA in lymphocytes of HIV-infected patients

被引:69
作者
Jaruga, P
Jaruga, B
Gackowski, D
Olczak, A
Halota, W
Pawlowska, M
Olinski, R
机构
[1] Ludwik Rydygier Med Univ, Dept Clin Biochem, PL-85092 Bydgoszcz, Poland
[2] Ludwik Rydygier Med Univ, Clin Infect Dis, Bydgoszcz, Poland
关键词
oxidative DNA damage; free radicals; IDUs; AIDS;
D O I
10.1016/S0891-5849(01)00821-8
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
There is evidence suggesting that patients infected with human immunodeficiency virus (HIV) are under chronic oxidative stress. In the present study, the level of oxidatively modified bases in lymphocyte DNA and some other parameters of oxidative stress were measured in HIV-infected patients (n = 30), as well as in control groups (10 healthy volunteers and 15 HIV-seronegative injected drug users). Additional experiments were conducted using lymphocyte DNA samples from asymptomatic seropositive, HIV-infected patients who were supplemented with antioxidant vitamins A, C, and E or received placebo. Significant increases in the amount of the modified DNA bases were observed in HIV-infected patients when compared with the control group. The concentration of thiobarbituric acid reactive substances (TBARS) was higher and activities of antioxidant enzymes (superoxide dismutase and catalase) were lower in the group of HIV-infected patients in comparison to the control group. Vitamin supplementation resulted in the significant decrease in the levels of all modified DNA bases when compared to the patients who received placebo. The reduction of TBARS and the restoration of the activity of the enzymes were also observed. Our data suggest that people infected with HIV can benefit from treatment with antioxidant vitamins. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:414 / 420
页数:7
相关论文
共 43 条
[1]  
AMEISEN JC, 1991, IMMUNOL TODAY, V12, P102
[2]   OXIDATIVE DNA-DAMAGE AND CELLULAR-SENSITIVITY TO OXIDATIVE STRESS IN HUMAN AUTOIMMUNE-DISEASES [J].
BASHIR, S ;
HARRIS, G ;
DENMAN, MA ;
BLAKE, DR ;
WINYARD, PG .
ANNALS OF THE RHEUMATIC DISEASES, 1993, 52 (09) :659-666
[3]   Dietary oxidative stress and the potentiation of viral infection [J].
Beck, MA ;
Levander, OA .
ANNUAL REVIEW OF NUTRITION, 1998, 18 :93-116
[4]   SOD2 - A NEW TYPE OF TUMOR-SUPPRESSOR GENE [J].
BRAVARD, A ;
SABATIER, L ;
HOFFSCHIR, F ;
RICOUL, M ;
LUCCIONI, C ;
DUTRILLAUX, B .
INTERNATIONAL JOURNAL OF CANCER, 1992, 51 (03) :476-480
[5]   The effects of vitamin C supplementation on protein oxidation in healthy volunteers [J].
Carty, JL ;
Bevan, R ;
Waller, H ;
Mistry, N ;
Cooke, M ;
Lunec, J ;
Griffiths, HR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (02) :729-735
[6]  
Centers for Disease Control, 1993, MMWR Morb Mortal Wkly Rep, V41, P1
[7]   Novel repair action of vitamin C upon in vivo oxidative DNA damage [J].
Cooke, MS ;
Evans, MD ;
Podmore, ID ;
Herbert, KE ;
Mistry, N ;
Mistry, P ;
Hickenbotham, PT ;
Hussieni, A ;
Griffiths, HR ;
Lunec, J .
FEBS LETTERS, 1998, 439 (03) :363-367
[8]   Ex vivo induction of apoptosis in lymphocytes is mediated by oxidative stress: Role for lymphocyte loss in HIV infection [J].
Dobmeyer, TS ;
Findhammer, S ;
Dobmeyer, JM ;
Klein, SA ;
Raffel, B ;
Hoelzer, D ;
Helm, EB ;
Kabelitz, D ;
Rossol, R .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (05) :775-785
[9]  
Duthie SJ, 1996, CANCER RES, V56, P1291
[10]   THE ROLE OF 8-HYDROXYGUANINE IN CARCINOGENESIS [J].
FLOYD, RA .
CARCINOGENESIS, 1990, 11 (09) :1447-1450