Vitamin E supplementation and oxidative damage to DNA and plasma LDL in type 1 diabetes

被引:51
作者
Astley, S
Langrish-Smith, A
Southon, S
Sampson, M
机构
[1] Norfolk & Norwich Healthcare NHS Trust, Bertram Diabet Res Unit, Norwich, Norfolk, England
[2] Inst Food Res, Norwich NR4 7UA, Norfolk, England
关键词
D O I
10.2337/diacare.22.10.1626
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To determine the effect of 400 IU/day of the antioxidant vitamin E on the susceptibility of plasma IDL and lymphocyte DNA to oxidative damage in type 1 diabetes. RESEARCH DESIGN AND METHODS - We studied 42 patients with type 1 diabetes and 31 age- and sex-matched control subjects in a randomized prospective double-blind placebo-controlled trial by using 400 IU/day of oral vitamin E for 8 weeks. Measurements were made of single-strand breaks in lymphocyte DNA at baseline and after hydrogen peroxide-induced stress (comet assay) and of copper-induced LDL oxidization and plasma antioxidant profiles. RESULTS - Plasma LDL and lymphocyte DNA were more resistant to induced oxidative change in the type 1 diabetes group than in control subjects. Vitamin E supplementation reduced LDL oxidizability in the control subjects but not in the type 1 diabetes group and had no effect on oxidative DNA damage in either group. The type 1 diabetes group had a significantly poorer plasma antioxidant profile with lower mean serum concentrations of alpha-tocopherol and most carotenoids than control subjects. CONCLUSIONS - Plasma LDL and lymphocyte DNA appear to be more resistant to oxidative change in type 1 diabetic subjects than in control subjects, and there was no evidence of oxidatively induced DNA or LDL change in type 1 diabetes. This study does not support the hypothesis of oxidative damage in these patients, and a dose of vitamin E (400 IU/day) that reduced LDL oxidative susceptibility in control subjects did not do so in patients with type 1 diabetes.
引用
收藏
页码:1626 / 1631
页数:6
相关论文
共 49 条
  • [1] ASTLEY S, 1996, THESIS U E ANGLIA NO
  • [2] Antioxidant status and lipid peroxidation in diabetic pregnancy
    Bates, JH
    Young, IS
    Galway, L
    Traub, AI
    Hadden, DR
    [J]. BRITISH JOURNAL OF NUTRITION, 1997, 78 (04) : 523 - 532
  • [3] ENHANCED SUSCEPTIBILITY OF LOW-DENSITY-LIPOPROTEIN TO IN-VITRO OXIDATION IN TYPE-1 AND TYPE-2 DIABETIC-PATIENTS
    BEAUDEUX, JL
    GUILLAUSSEAU, PJ
    PEYNET, J
    FLOURIE, F
    ASSAYAG, M
    TIELMANS, D
    WARNET, A
    ROUSSELET, F
    [J]. CLINICA CHIMICA ACTA, 1995, 239 (02) : 131 - 141
  • [4] GLYCOSYLATED LOW-DENSITY-LIPOPROTEIN IS MORE SENSITIVE TO OXIDATION - IMPLICATIONS FOR THE DIABETIC PATIENT
    BOWIE, A
    OWENS, D
    COLLINS, P
    JOHNSON, A
    TOMKIN, GH
    [J]. ATHEROSCLEROSIS, 1993, 102 (01) : 63 - 67
  • [5] DIRECT ENZYMATIC DETECTION OF ENDOGENOUS OXIDATIVE BASE DAMAGE IN HUMAN LYMPHOCYTE DNA
    COLLINS, AR
    DUTHIE, SJ
    DOBSON, VL
    [J]. CARCINOGENESIS, 1993, 14 (09) : 1733 - 1735
  • [6] The comet assay: What can it really tell us?
    Collins, AR
    Dobson, VL
    Dusinska, M
    Kennedy, G
    Stetina, R
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 375 (02) : 183 - 193
  • [7] Oxidative damage to DNA: Do we have a reliable biomarker?
    Collins, AR
    Dusinska, M
    Gedik, CM
    Stetina, R
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1996, 104 : 465 - 469
  • [8] Cominacini L, 1994, Diabetes Res, V26, P173
  • [9] Oxidative damage to DNA in diabetes mellitus
    Dandona, P
    Thusu, K
    Cook, S
    Snyder, B
    Makowski, J
    Armstrong, D
    Nicotera, T
    [J]. LANCET, 1996, 347 (8999) : 444 - 445
  • [10] INSULIN-STIMULATED GLUCOSE-TRANSPORT IN CIRCULATING MONONUCLEAR-CELLS FROM NONDIABETIC AND IDDM SUBJECTS
    DANEMAN, D
    ZINMAN, B
    ELLIOTT, ME
    BILAN, PJ
    KLIP, A
    [J]. DIABETES, 1992, 41 (02) : 227 - 234