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INTERVAL TRAINING IS INSUFFICIENT TO ATTENUATE METABOLIC DISTURBANCES IN DIABETIC RATS

TREINAMENTO INTERVALADO É INSUFICIENTE PARA ATENUAR DISTÚRBIOS METABÓLICOS EM RATOS DIABÉTICOS

ENTRENAMIENTO A INTERVALOS ES INSUFICIENTE PARA ATENUAR TRASTORNOS METABÓLICOS EN RATAS DIABÉTICAS

ABSTRACT

Introduction:

Type 1 diabetes is a metabolic disease associated to blood disturbances and disorder of the innate immune system functionality.

Objective:

This study investigated the effect of two weeks interval training on blood biochemistry and immunological parameters in rats with type 1 diabetes.

Methods:

Male Wistar rats were divided into three groups: sedentary (SE, n = 10), diabetic sedentary (DI, n = 10), diabetic interval training (DIT, n = 10). IV injection of streptozotocin (45 mg/kg) induced diabetes. Interval training consisted of swimming exercise for 30 seconds with 30 seconds of rest for 30 minutes three times a week during two weeks, with an overload of 15% of the total body mass. The evaluations performed were fasting blood glucose, triglycerides, very low-density lipoprotein cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol and total cholesterol concentrations, phagocytic capacity, cationic vesicles content, superoxide anion, and production of hydrogen peroxide of blood neutrophils and peritoneal macrophages.

Results:

The results showed that two weeks interval training did not attenuate the hyperglycemic state at rest and did not decrease blood lipids in the DIT group. Diabetes increased the functionality of blood neutrophils and peritoneal macrophages in the DI group. Interval training increased the content of cationic vesicles and the phagocytic capacity of blood neutrophils and peritoneal macrophages in the DIT group.

Conclusion:

It was found that two weeks of interval training increased the functionality parameters of innate immune cells, although this has been insufficient to attenuate the biochemical disorders caused by diabetes.

Keywords:
diabetes mellitus; immune system; hyperglycemia

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