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Long-term correction of STZ-diabetic rats after short-term i.p. VOSO4 treatment: Persistence of insulin secreting capacities assessed by isolated pancreas studies

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Abstract

We have previously shown that 3 week oral VOSO4 treatment of streptozotocin (STZ, 60 mg/kg)-induced diabetic rats was able to correct diabetes for 13 weeks after treatment withdrawal. In the present study, we investigated whether a short-term (8 days) i.p. VOSO4 treatment was similarly able to reverse the diabetic state. Insulin secretory capacities were assessed at distance of treatment using the isolated pancreas preparation. Seven treatment-groups were performed: high dose VOSO4 -treated diabetics (HVD, 1.3 mM/kg/8 days), food-restricted diabetics (FRD, food adjusted to HVD levels), low dose VOSO4 -treated diabetes (LVD, 0.06 mM/kg/day), insulin-treated diabetics (ID, dose adjusted to normalize glycaemia) and VOSO4 (0.06 mM/kg/day) + insulin (dose adjusted to normalize glycaemia in the presence of vanadium)-treated diabetics (IVD), in addition to the corresponding untreated non-diabetic controls (C) and diabetics (D). Our results indicate that long-term correction of diabetes (a) can be obtained after an 8 day treatment using i.p. VOSO4 in diabetic animals retaining some degree of pancreatic function, (b) is not obtained with insulin treatment or food restriction although the association of VOSO4 and insulin was found beneficial, (c) can be prolonged in some individuals for at least 4 months, i.e. in conditions such that tissue vanadium concentrations had returned to values close to pre-treatment levels, (d) is associated with improved and in some cases normalized insulin secretion from isolated pancreas. The protective or corrective role of VOSO4 on diabetes-related pancreatic alterations, as well as the potential of the VOSO4 -insulin association should be further studied in view of the possible use of vanadium derivatives in the treatment of diabetes.

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References

  1. Shechter Y, Karlish SJD: Insulin-like stimulation of glucose oxydation in rat adipocytes by vanadyl (IV) ion. Nature 284: 556–558, 1980

    Article  PubMed  CAS  Google Scholar 

  2. Rodriguez-Gil JE, Gomez-Foix AM, Fillat C, Bosch F, Guinovart J-J: Activation by vanadate of glycolysis in hepatocytes from diabetic rats. Diabetes 40: 1355–1359, 1991

    Article  PubMed  CAS  Google Scholar 

  3. Aguis L, Vaartjes WJ: The effects of orthovanadate on fatty acid synthesis in isolated rat hepatocytes. Biochem. J. 202: 791–794, 1982

    Google Scholar 

  4. Castro J, Maquedano A, Olive M: Lipid synthesis in isolated rat hepatocytes: activation by insulin and vanadate and inhibition by ouabain. Biochem Inter 9: 413–420, 1984

    CAS  Google Scholar 

  5. Ramanadham S, Mongold JJ, Brownsey R, Cros GH, McNeill JH: Oral vanadyl sulfate in treatment o diabetes mellitus in rats. Am. J. Physiol. 257 (Heart Circ. Physiol. 26): H904-H911, 1989

    PubMed  CAS  Google Scholar 

  6. Sakurai H, Tschiya K, Nukatsuka M, Sofue M, Kawada J: Insulinlike effect of vanadyl ion on streptozotocin-induced diabetic rats. J. Endocrinol 126: 451–459, 1990

    Article  PubMed  CAS  Google Scholar 

  7. Heyliger CE, Tahiliani AG, McNeill JH: Effect of vanadate on elevated blood glucose and depressed cardiac performance of diabetic rats. Science 227: 1474–1477, 1985

    Article  PubMed  CAS  Google Scholar 

  8. Meyerovitch J, Farfel Z, Sack J, Shechter Y: Oral administration of vanadate normalizes blood glucose levels in streptozotocin-diabetic rats. Characterization and mode of action. J Biol Chem 262: 6658–3662, 1987

    PubMed  CAS  Google Scholar 

  9. Shisheva A, Ikonomov O, Shechter Y: The protein phosphatase inhibitor, pervanadate, is a powerful antidiabetic agent in streptoztocin-treated rats. Endocrinlogy 134: 507–510, 1994

    Article  CAS  Google Scholar 

  10. Meyerovitch J, Rothenberg P, Shechter T, Bonner-Weir S, Kahn CR: Vanadate normalizes hyperglycemia in two mouse models of non-insulin-dependent diabetes mellitus. J Clin Invest 87: 1286–1294, 1991

    Article  PubMed  CAS  Google Scholar 

  11. Pugazhenthi S, Angel JF, Khandelwal RL: Long-term effects of vanadate treatment on glycogen metabolizing and lipogenic enzymes of liver in genetically diabetic (db/db) mice. Metabolism 40: 941–946, 1991

    Article  PubMed  Google Scholar 

  12. Battell ML, Yuen VG, McNeill JH: Treatment of BB rats with vanadyl sulfate. Pharmacol Commun 1: 291–301, 1992

    CAS  Google Scholar 

  13. Ramanadham S, Cros GH, Mongold JJ, Serrano JJ, McNeill JH: Enhanced in vivo sensitivity of vanadyl-treated diabetic rats to insulin. Can J Physiol Pharmacol 68: 486–491, 1990

    Article  PubMed  CAS  Google Scholar 

  14. Ramanadham S, Brownsey RW, Cros GH, Mongold J-J, McNeill JH: Sustained prevention of myocardial and metabolic abnormalities in diabetic rats following withdrawal from oral vanadyl treatment. Metabolism 38: 1022–1028, 1989

    Article  PubMed  CAS  Google Scholar 

  15. Dai S, Thompson KH, McNeill JH: One-year treatment of Streptozotocin-induced diabetic rats with vanadyl sulfate. Pharmacology and Toxicology 74: 101–109, 1994

    Article  PubMed  CAS  Google Scholar 

  16. Cam MC, Faun J, McNeill JH: Concentration-dependent glucose lowering effects of oral vanadyl are maintained following treatment withdrawal in streptozotocin-diabetic rats. Metab Clin Exp 44: 332–339, 1995

    PubMed  CAS  Google Scholar 

  17. Pederson RA, Ramanadham S, Buchan AMJ, McNeill JH: Long-term effects of vanadyl treatment on streptozotocin-induced diabetes in rats. Diabetes 38: 1390–1395, 1989

    Article  PubMed  CAS  Google Scholar 

  18. LoubatieresA, Mariani MM, Ribes G, De Malbosc H, Chapal J: Etude expérimentale d’un noueau sulfamide hypoglycémiant particulièrement actif, le HB 419 ou glibenclamide. I. Action betacytotrope et insulinosécrétrice. Diabetologia 5: 1–10, 1969

    Article  Google Scholar 

  19. Herbert V, Lau KS, Gottlieb CW, Bleicher SJ: Coated charcoal immunoassay of insulin. J Clin Endocrinol Metab 25: 1375–1384, 1965

    Article  PubMed  CAS  Google Scholar 

  20. Mongold JJ, Cros GH, Vian L, Tep A, Ramanadham S, Siou G, Diaz J, McNeill JH, Serrano JJ: Toxicological aspects of vanadyl sulfate on diabetic rats: effects on vanadium levels and pancreatic B-cell morphology. Pharmacol Toxicol: 67: 192–198, 1990

    Article  PubMed  CAS  Google Scholar 

  21. Unger RH, Grundy: Hyperglycemia as an inducer as well as a consequence of impaired islet cell function and insulin resistance: implication for the management of diabetes. Diabetologia 28: 119–121, 1985

    Article  PubMed  CAS  Google Scholar 

  22. Guastamacchia E, Ciampolillo A, Lattanzi V, Lollino G, Rosco M, Lucivero G, Dell’Osso A, Giorgino R, Nardelli GM: In search of predictive markers of remission from insulin dependence in type 1 diabetes: a preliminary report. Diab Res Clin Pract 16: 145–149, 1992

    Article  CAS  Google Scholar 

  23. Buschard K: The functional state of the beta-cells in the pathogenesis of insulin-dependent diabetes mellitus. Autoimmunity 10:65–69, 1991

    Article  PubMed  CAS  Google Scholar 

  24. Malabu UH, Dryden S, McCarthy DMC, Kilpatrick A, Williams G: Effects of chronic vanadate administration in the STZ-induced diabetic rat. The antihyperglycemic action of vanadate is attributable entirely to its suppression of feeding. Diabetes 43: 9–15, 1994

    Article  PubMed  CAS  Google Scholar 

  25. Parker RDR, Shama RP: Accumulation and depletion of vanadium in selected tissues of rats treated with vanadyl sulfate and sodium orthovanadate. J Environ Pathol Toxicol 2: 235–245, 1978

    PubMed  CAS  Google Scholar 

  26. Al-Bayati M, Raabe OG, Giri SN, Knaak JB: Distribution of vanadate in the rat following subcutaneous an oral routes of administration. J Am Coll Toxicol 10: 233–241, 1991

    CAS  Google Scholar 

  27. Fagin JA, Ikejiri K, Levin SR: Insulinotropic effects of vanadate. Diabetes 36: 1448–1452, 1991

    Article  Google Scholar 

  28. Zhang A, Gao Z-Y, Gilon P, Nenquin M, Drews G, Henquin JC: Vanadate stimulation of insulin release in normal mouse islets. J Biol Chem 266: 21649–21656, 1991

    PubMed  CAS  Google Scholar 

  29. Voss C, Herrmann I, Hartmann K, Zuhlke H: In vitro effect of vanadate on content, secretion and biosynthesis of insulin in isolated islets of normal Wistar rats. Exp Clin Endocrinol 99: 159–163, 1992

    Article  PubMed  CAS  Google Scholar 

  30. Cam MC, Pederson RA, Brownsey RW, McNeill JH: Long-term effectiveness of oral vanadyl sulphate in streptozotocin-diabetic rats. Diabetologia 36: 218–224, 1993

    Article  PubMed  CAS  Google Scholar 

  31. Rijksen G, Voller M VW, Van Zoellen EJJ: Orthovanadate both mimics and antagonizes the transforming growth factor z action on normal rat kidney cells. J Cell Physiol 154: 393–401, 1993

    Article  PubMed  CAS  Google Scholar 

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© 1995 Kluwer Academic Publishers

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Poucheret, P. et al. (1995). Long-term correction of STZ-diabetic rats after short-term i.p. VOSO4 treatment: Persistence of insulin secreting capacities assessed by isolated pancreas studies. In: Srivastava, A.K., Chiasson, JL. (eds) Vanadium Compounds: Biochemical and Therapeutic Applications. Developments in Molecular and Cellular Biochemistry, vol 16. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-1251-2_26

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  • DOI: https://doi.org/10.1007/978-1-4613-1251-2_26

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4612-8533-5

  • Online ISBN: 978-1-4613-1251-2

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