Tungstate is an effective antidiabetic agent in streptozotocin-induced diabetic rats:: a long-term study

被引:72
作者
Barberà, A
Gomis, RR
Prats, N
Rodríguez-Gil, JE
Domingo, M
Gomis, R
Guinovart, JJ
机构
[1] Univ Barcelona, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
[2] Autonomous Univ Barcelona, Dept Histol & Anim Pathol, E-08193 Barcelona, Spain
[3] Autonomous Univ Barcelona, Dept Anim Reprod, E-08193 Barcelona, Spain
[4] Hosp Clin & Univ, Agusti Pi & Sunyer Inst Biomed Res, Dept Med, Endocrinol & Diabet Unit, Barcelona, Spain
关键词
tungstate; STZ-diabetic rats; liver; insulin-like; glucose metabolism; glycaemia;
D O I
10.1007/s001250100479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. Recent studies have shown the anti diabetic effects of oral sodium tungstate treatment in several animal models of diabetes based on short-term experiments. In this study, we examined the effectiveness of long-term tungstate treatment of streptozotocin-induced-diabetic rats. Methods. Tungstate was administered to the drinking water of rats for eight months. Results. The treatment resulted in a reduction in serum glucose concentrations in diabetic rats, but no change in glycaemia was detected in healthy rats. Alterations in the hepatic glucose metabolism due to diabetes were almost completely counteracted by tungstate treatment. The partial recovery of glucokinase activity, not found in diabetic animals, normalised glycogen and glucose 6-phosphate concentrations. Tungstate treatment also restored pyruvate kinase activity and fructose 2,6-bisphosphate concentrations. In healthy rats, tungstate treatment did not modify the majority of the hepatic parameters studied, Moreover, tungstate treatment prevented diabetes-induced morphological changes in the kidney and ocular lens and also reduced mortality. Furthermore, no hypoglycaemic episodes or undesirable side effects were observed in treated diabetic or healthy rats. In addition, there is no evidence of intolerance developing after prolonged use. Conclusion/interpretation. Tungstate could play a helpful part in the long-term treatment of diabetes.
引用
收藏
页码:507 / 513
页数:7
相关论文
共 34 条
  • [1] BARBERA A, 1994, J BIOL CHEM, V269, P20047
  • [2] Effects of tungstate in neonatally streptozotocin-induced diabetic rats: Mechanism leading to normalization of glycaemia
    Barbera, A
    FernandezAlvarez, J
    Truc, A
    Gomis, R
    Guinovart, JJ
    [J]. DIABETOLOGIA, 1997, 40 (02) : 143 - 149
  • [3] Sodium selenate corrects glucose tolerance and heart function in STZ diabetic rats
    Battell, ML
    Delgatty, HLM
    McNeill, JH
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 179 (1-2) : 27 - 34
  • [4] Oral selenate improves glucose homeostasis and partly reverses abnormal expression of liver glycolytic and gluconeogenic enzymes in diabetic rats
    Becker, DJ
    Reul, B
    Ozcelikay, AT
    Buchet, JP
    Henquin, JC
    Brichard, SM
    [J]. DIABETOLOGIA, 1996, 39 (01) : 3 - 11
  • [5] THE ROLE OF VANADIUM IN THE MANAGEMENT OF DIABETES
    BRICHARD, SM
    HENQUIN, JC
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1995, 16 (08) : 265 - 270
  • [6] BURCELIN R, 1995, DIABETOLOGIA, V38, P283, DOI 10.1007/BF00400632
  • [7] Distinct glucose lowering and beta cell protective effects of vanadium and food restriction in streptozotocin-diabetes
    Cam, MC
    Rodrigues, B
    McNeill, JH
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1999, 141 (05) : 546 - 554
  • [8] RAPID METHOD FOR DETERMINATION OF GLYCOGEN CONTENT AND RADIOACTIVITY IN SMALL QUANTITIES OF TISSUE OR ISOLATED HEPATOCYTES
    CHAN, TM
    EXTON, JH
    [J]. ANALYTICAL BIOCHEMISTRY, 1976, 71 (01) : 96 - 105
  • [9] Cryer PE, 1999, DIABETES-METAB RES, V15, P42, DOI 10.1002/(SICI)1520-7560(199901/02)15:1<42::AID-DMRR1>3.0.CO
  • [10] 2-B