RESUMO
The chronic use of Dexamethasone (Dex) induced hyperglycemia and insulin resistance. On the other hand, physical exercise attenuates the symptoms induced by Dex in many physiological systems. However, the effect of the exercise on the changes in gastric motility induced by dexamethasone remains unknown. We hypothesized that low-intensity aerobic exercise modulates the metabolic effects induced by Dex-treatment by modifying the gastrointestinal function and feeding behavior in rats. Male rats were distributed into the following groups: Control (Ctrl), Dex (1.0â¯mg/kg, i.p.), Exercise (Ctrlâ¯+â¯Exercise 5%) and (Dex1.0â¯+â¯Exercise 5%). The exercise protocol was swimming for 5 consecutive days. We assessed the murinometric and nutritional indices, food intake, blood glucose by (ipGTT) and the gastric emptying rate of a liquid test meal were assessed in all rats. We observed a significant decrease (pâ¯<â¯.05) in the gastric emptying in Dex1.0â¯group in relation to Ctrl group. The exercise prevented decrease in the gastric emptying (pâ¯<â¯.05) in Dex1.0â¯+â¯EX5% group when compared with Dex1.0â¯groups. The Dex1.0â¯group induced a significantly increase (pâ¯<â¯.05) in glycaemia vs Ctrl group. The hyperglycemia was improving (pâ¯<â¯.05) in the Dex1.0â¯+â¯Ex5% compared with Dex1.0â¯groups. We observed a positive correlation (pâ¯<â¯.05, and râ¯=â¯0.7065) between gastric retention vs glycaemia in the Dex1.0â¯groups. The Dex1.0 reduced (pâ¯<â¯.05) the body weight and altered body composition, promoting hypophagia. IL-6 increased (pâ¯<â¯.05) at gastric fundus in Ex5% compared with Ctrl groups. In conclusion, the use of Dex1.0 decreases gastric emptying, promotes hyperglycemia and modifies feeding behavior. The low-intensity exercise prevents hyperglycemia, thus improving gastric dysmotility without improving the anthropometric parameters.