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HEPATIC AND SKELETAL MUSCLE TISSUE IMMUNOMETABOLISM IN TRAINED RATS

INMUNOMETABOLISMO DEL TEJIDO HEPÁTICO Y MUSCULAR ESQUELÉTICO DE RATAS ENTRENADAS

ABSTRACT

Introduction:

Physical exercise can be an alternative for preventing and treating the harmful effects of obesity, mainly inflammatory effects on skeletal muscle and liver tissues. However, no consensus exists regarding this purpose's best physical training model.

Objective:

Evaluate morphological, metabolic, and inflammatory alterations in rats’ skeletal and hepatic muscle tissues caused by aerobic and resistance training.

Methods:

24 Wistar rats were divided into sedentary (S), aerobic (AE), and resistance training (R) groups. Blood glucose, total cholesterol, and serum triglycerides were measured periodically. After euthanasia, body mass was measured to calculate the total mass gain during the experiment. High-density lipoprotein (HDL) was measured. Adipose tissue was extracted to calculate its percentage relative to body mass and the liver, soleus, and gastrocnemius muscles for morphological analyses and concentrations of glycogen, lipids, and Tumor Necrosis Factor α (TNF-α). The Kruskall-Wallis test and Dunn's post-test were performed for statistical analysis, adopting p<0.05.

Results:

Both training models reduced the percentage of adipose tissue, body mass gain, and hepatic TNF-α concentration (p<0.05). AE increased serum HDL, gastrocnemius fiber diameter and reduced the fractal dimension in the soleus (p<0.05). R reduced blood glucose and serum and liver lipids, increased liver and soleus glycogen concentrations, increased gastrocnemius fiber diameter, and decreased TNF-α (p<0.05).

Conclusion:

Both training models reduced body mass, relative visceral adipose tissue, serum total cholesterol concentration, and liver inflammation. However, resistance training was more effective in promoting metabolic effects in the liver and skeletal muscle and reducing muscle inflammation in rats. Level of Evidence V; Expert Opinion.

Keywords:
Resistance Training; Liver; Muscle, Skeletal; Tumor Necrosis Factor-alpha

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