Preventive aspirin treatment of streptozotocin induced diabetes: blockage of oxidative status and revertion of heme enzymes inhibition

被引:41
作者
Caballero, F [1 ]
Gerez, E [1 ]
Batlle, A [1 ]
Vazquez, E [1 ]
机构
[1] Univ Buenos Aires, FCEN, Dept Biol, Ctr Invest Porfirinas & Porfirias, RA-1428 Buenos Aires, DF, Argentina
关键词
experimental diabetes mellitus; acetylsalicylic acid; heme enzymes inactivation; glycation; lipid peroxidation; oxidative stress;
D O I
10.1016/S0009-2797(00)00168-X
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
Some late complications of diabetes are associated with alterations in the structure and function of proteins due to glycation and free radicals generation. Aspirin inhibits protein glycation by acetylation of free amino groups. In the diabetic status, it was demonstrated that several enzymes of heme pathway were diminished. The aim of this work has been to investigate the in vivo effect of short and long term treatment with acetylsalicylic acid in streptozotocin induced diabetic mice. In both treatments, the acetylsalicylic acid prevented delta-aminolevulinic dehydratase and porphobilinogen deaminase inactivation in diabetic mice and blocked the accumulation of lipoperoxidative aldehydes. Catalase activity was significantly augmented in diabetic mice and the long term treatment with aspirin partially reverted it. We propose that oxidative stress might play an important role in streptozotocin induced diabetes. Our results suggest that aspirin can prevent some of the late complications of diabetes, lowering glucose concentration and probably inhibiting glycation by acetylation of protein amino groups. (C) 2000 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:215 / 225
页数:11
相关论文
共 35 条
  • [1] Bastar I, 1998, RES COMMUN MOL PATH, V102, P265
  • [2] PURIFICATION AND GENERAL PROPERTIES OF DELTA-AMINOLAEVULATE DEHYDRATASE FROM COW LIVER
    BATLLE, AMD
    FERRAMOLA, AM
    GRINSTEIN, M
    [J]. BIOCHEMICAL JOURNAL, 1967, 104 (01) : 244 - +
  • [3] BATLLE AMDC, 1978, INT J BIOCHEM, V9, P871
  • [4] ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES
    BAYNES, JW
    [J]. DIABETES, 1991, 40 (04) : 405 - 412
  • [5] DIABETES-INDUCED METABOLIC ALTERATIONS IN HEME-SYNTHESIS AND DEGRADATION AND VARIOUS HEME-CONTAINING ENZYMES IN FEMALE RATS
    BITAR, M
    WEINER, M
    [J]. DIABETES, 1984, 33 (01) : 37 - 44
  • [6] In vitro kinetic studies of formation of antigenic advanced glycation end products (AGEs) - Novel inhibition of post-Amadori glycation pathways
    Booth, AA
    Khalifah, RG
    Todd, P
    Hudson, BG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) : 5430 - 5437
  • [7] LILLY LECTURE 1993 - GLYCATION AND DIABETIC COMPLICATIONS
    BROWNLEE, M
    [J]. DIABETES, 1994, 43 (06) : 836 - 841
  • [8] CABALLERO F, 1995, MEDICINA-BUENOS AIRE, V55, P117
  • [9] Reducing sugars trigger δ-aminolevulinic dehydratase inactivation:: Evidence of in vitro aspirin prevention
    Caballero, FA
    Gerez, EN
    Polo, CF
    Vazquez, ES
    Batlle, AMD
    [J]. GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1998, 31 (03): : 441 - 445
  • [10] ASSAY OF CATALASES AND PEROXIDASES
    CHANCE, B
    MAEHLY, AC
    [J]. METHODS IN ENZYMOLOGY, 1955, 2 : 764 - 775