Oxidative damage, plasma antioxidant capacity, and glucemic control in elderly NIDDM patients

被引:55
作者
Aguirre, F
Martin, I
Grinspon, D
Ruiz, M
Hager, A
De Paoli, T
Ihlo, J
Farach, HA
Poole, CP
机构
[1] Univ Buenos Aires, Hosp Clin Jose de San Martin, RA-1053 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Fis, RA-1053 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, RLBM, LANAIS, RA-1053 Buenos Aires, DF, Argentina
[4] Univ S Carolina, Dept Phys & Astron, Columbia, SC 29208 USA
关键词
free radical; lipid peroxidation; diabetes mellitus; erythrocyte; low-density lipoproteins;
D O I
10.1016/S0891-5849(97)00293-1
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
A study of oxidative damage was made in elderly noninsulin-dependent diabetes mellitus (NIDDM) patients. A statistically significant increase in glucose and fructosamine was found in fasting NIDDM patients, as well as an increase in the oxidation induced by tert-butyl hydroperoxide. The Total Reactive Antioxidant Potential (TRAP) of the plasma was much reduced (p < .02) and the uricemia was unchanged. The erythrocytes of diabetic patients show greater basal oxidation products (p < .05), and the susceptibility of the diabetic erythrocytes to oxidation injury was also shown to increase in the oxidation induced by t-BOOH (p < .05). Linear regression studies showed that TRAP was associated directly with uric acid (p < .05) and inversely with fructosamine and with glucose (p < .03 and p < .05 respectively) in patients with NIDDM, but not in the controls, The levels of fructosamine were found to be related to the basal damage of the red blood cells (direct correlation, p < .001). This study suggest an useful approach to diabetic oxidative stress for clinical settings. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:580 / 585
页数:6
相关论文
共 29 条
  • [1] AGUIRRE F, 1992, REUN AN SOC ARG BIOF
  • [2] ANTIOXIDANTS IN THE SERUM OF CHILDREN WITH INSULIN-DEPENDENT DIABETES-MELLITUS
    ASAYAMA, K
    UCHIDA, N
    NAKANE, T
    HAYASHIBE, H
    DOBASHI, K
    AMEMIYA, S
    KATO, K
    NAKAZAWA, S
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1993, 15 (06) : 597 - 602
  • [3] ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES
    BAYNES, JW
    [J]. DIABETES, 1991, 40 (04) : 405 - 412
  • [4] GLYCATION PRODUCTS AND THE PATHOGENESIS OF DIABETIC COMPLICATIONS
    BROWNLEE, M
    [J]. DIABETES CARE, 1992, 15 (12) : 1835 - 1843
  • [5] LILLY LECTURE 1993 - GLYCATION AND DIABETIC COMPLICATIONS
    BROWNLEE, M
    [J]. DIABETES, 1994, 43 (06) : 836 - 841
  • [6] CADENAS E, 1985, OXIDATIVE STRESS
  • [7] ACCUMULATION OF MAILLARD REACTION-PRODUCTS IN SKIN COLLAGEN IN DIABETES AND AGING
    DYER, DG
    DUNN, JA
    THORPE, SR
    LYONS, TJ
    MCCANCE, DR
    BAYNES, JW
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1992, 663 : 421 - 422
  • [8] SALICYLATE HYDROXYLATION AS AN EARLY MARKER OF INVIVO OXIDATIVE STRESS IN DIABETIC-PATIENTS
    GHISELLI, A
    LAURENTI, O
    DEMATTIA, G
    MAIANI, G
    FERROLUZZI, A
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1992, 13 (06) : 621 - 626
  • [9] Oxidative stress and diabetic vascular complications
    Giugliano, D
    Ceriello, A
    Paolisso, G
    [J]. DIABETES CARE, 1996, 19 (03) : 257 - 267
  • [10] GLUCOSE-OXIDATION AND LOW-DENSITY LIPOPROTEIN-INDUCED MACROPHAGE CEROID ACCUMULATION - POSSIBLE IMPLICATIONS FOR DIABETIC ATHEROSCLEROSIS
    HUNT, JV
    BOTTOMS, MA
    CLARE, K
    SKAMARAUSKAS, JT
    MITCHINSON, MJ
    [J]. BIOCHEMICAL JOURNAL, 1994, 300 : 243 - 249