Urinary excretion of glycosaminoglycans and albumin in experimental diabetes mellitus

被引:30
作者
Cadaval, RAM
Kohlman, O
Michelacci, YM
机构
[1] Univ Fed Sao Paulo, Escola Paulista Med, Disciplina Biol Mol, Dept Bioquim, BR-04023020 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Escola Paulista Med, Dept Med, Disciplina Nefrol, BR-04023020 Sao Paulo, Brazil
关键词
albuminuria; diabetes mellitus; glycosaminoglycan; kidney; urine;
D O I
10.1093/glycob/10.2.185
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
Diabetes mellitus was induced in one group of rats by a single injection of streptozotocin. The glycemia, the body weight, and the blood systolic pressure were measured every week, and the 24 h urine volume and urinary excretions of creatinine, albumin and glycosaminoglycans were measured every 2 weeks, At the end of the experiment (12 weeks) the weight and the glycosaminoglycan composition of the kidneys were determined. All the diabetic animals were hyperglycemic, hypertense, and did not gain weight during all the experimental period. Albuminuria appeared from the second week on. Rat urine was shown to contain heparan sulfate, chondroitin sulfate, and dermatan sulfate, and the glycosaminoglycan excretion decreased in all diabetic animals. The onset of the change in glycosaminoglycan excretion rate was a very early event, appearing in the second week after diabetes induction. The main glycosaminoglycan found in normal rat kidney was heparan sulfate and, in contrast to the urine, the total kidney glycosaminoglycans increased in diabetic kidney, due to chondroitin sulfate and dermatan sulfate accumulation. The heparan sulfate concentration (per tissue dry weight) did not change. Our results suggest that quantification of urinary glycosaminoglycans may be a useful tool for the early diagnosis of diabetic nephropathy.
引用
收藏
页码:185 / 192
页数:8
相关论文
共 56 条
  • [1] Expression of laminin and type IV collagen by basement membrane-producing EHS tumors in streptozotocin-Induced diabetic mice: In vivo modulation by low-molecular-weight heparin fragments
    AsselotChapel, C
    Borchiellini, C
    LabatRobert, J
    Kern, P
    [J]. BIOCHEMICAL PHARMACOLOGY, 1996, 52 (11) : 1695 - 1701
  • [2] INCREASED EXTRACELLULAR-MATRIX SYNTHESIS AND MESSENGER-RNA IN MESANGIAL CELLS GROWN IN HIGH-GLUCOSE MEDIUM
    AYO, SH
    RADNIK, RA
    GLASS, WF
    GARONI, JA
    RAMPT, ER
    APPLING, DR
    KREISBERG, JI
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02): : F185 - F191
  • [3] TRANSFORMING GROWTH FACTOR-B REGULATES PRODUCTION OF PROTEOGLYCANS BY MESANGIAL CELLS
    BORDER, WA
    OKUDA, S
    LANGUINO, LR
    RUOSLAHTI, E
    [J]. KIDNEY INTERNATIONAL, 1990, 37 (02) : 689 - 695
  • [4] BOSSOLAN D, 1991, HYPERTENSION, V17, P461
  • [5] BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
  • [6] CASSARO CMF, 1977, J BIOL CHEM, V252, P2254
  • [7] Decrease in the glycosaminoglycan content in the skin of diabetic rats. The role of IGF-I, IGF-binding proteins and proteolytic activity
    CechowskaPasko, M
    Palka, J
    Bankowski, E
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1996, 154 (01) : 1 - 8
  • [8] Daimon S, 1998, CLIN NEPHROL, V49, P145
  • [9] Molecular biology of diabetic glomerulosclerosis
    Del Prete, D
    Anglani, F
    Ceol, M
    D'Angelo, A
    Forino, M
    Vianello, D
    Baggio, B
    Gambaro, G
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 1998, 13 : 20 - 25
  • [10] CELL RECOGNITION AND ADHESIVENESS - POSSIBLE BIOLOGICAL ROLE FOR SULFATED MUCOPOLYSACCHARIDES
    DIETRICH, CP
    SAMPAIO, LO
    TOLEDO, OMS
    CASSARO, CMF
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 75 (02) : 329 - 336