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.
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-diabeticrats. 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 diabeticrats, 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.
Authors: Douglas Nesadal de Souza; Eugen Mendes Nesadal de Souza; Marlus da Silva Pedrosa; Fernando Neves Nogueira; Alyne Simões; José Nicolau Journal: Biol Trace Elem Res Date: 2020-06-29 Impact factor: 3.738
Authors: F N Pardo; J Altirriba; M Pradas-Juni; A García; U Ahlgren; A Barberà; J C Slebe; A J Yáñez; R Gomis; R Gasa Journal: Diabetologia Date: 2012-08-29 Impact factor: 10.122
Authors: J Fernández-Alvarez; A Barberà; B Nadal; S Barceló-Batllori; S Piquer; M Claret; J J Guinovart; R Gomis Journal: Diabetologia Date: 2004-02-14 Impact factor: 10.122