Sulfonylurea induction of caffeine-enhanced insulin secretion and reduction of glycemic levels in diabetic rats

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Abstract

Context: Caffeine can stimulate insulin secretion by attenuating hyperglycemia in diabetes models with significant reduction of pancreatic functional β cells. Knowledge of these mechanisms could contribute to new strategies for treating diabetes. Objective: This study evaluated the effects of caffeine and physical exercise on glycemic and insulin responses in diabetic rats. Materials and methods: The diabetes model was induced by intraperitoneal administration of 60mg/kg of streptozotocin (STZ). Animals were divided into six groups: control, caffeine, STZ control, STZ caffeine, STZ sulfonylurea, and STZ caffeine+sulfonylurea. Acutely, control animals received 6mg of caffeine and 10mg/kg sulfonylurea or 10mg/kg saline. Animals were sacrificed after physical exercise; blood samples were collected for glucose, glycerol, lactate, and insulin analyses. Cardiovascular responses were recorded before and after treatments. A one-way ANOVA and the post hoc Student-Newman-Keuls test were used to analyze statistical differences between treatments (p<0.05). Results: About 6mg/kg of caffeine did not alter cardiovascular responses, but promoted blood glucose reduction after 60min of exercise when compared to animals in the control groups (387-187mg/dL; p<0.05). Insulin levels increased significantly (0.6-10μU/mL; p<0.05) in rats that received acute caffeine treatment associated with sulfonylurea compared to rats in the other groups. Discussion and conclusion: Acute caffeine intake with exercise can increase glucose uptake enhancing insulin secretion stimulated by sulfonylurea in β cells-deficient pancreas. The results indicate the potential use of caffeine as a strategy for glycemic and insulin control in diabetes. © 2014 Informa Healthcare USA, Inc.

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Da Silva, L. A., Pereira, R. A., Túrmina, J. A., Kerppers, I. I., Osiecki, R., Altimari, L. R., & Malfatti, C. R. M. (2014). Sulfonylurea induction of caffeine-enhanced insulin secretion and reduction of glycemic levels in diabetic rats. Pharmaceutical Biology, 52(8), 956–960. https://doi.org/10.3109/13880209.2013.874462

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