Therapeutic immobilization is a common treatment for the locomotor system; however, it causes loss of muscle due to disuse, leading to protein degradation and generating atrophy of muscle cells, ultimately changing functionality. In this sense, it is important for remobilization to be initiated early and performed with appropriate therapeutic strategies that enable tissue and functional recovery. One method of remobilization is physical exercise, among which whole body vibration (WBV) has been highlighted and mainly applied in people with reduced mobility. However, there are gaps on the morphological effects WBV has on muscle tissue, so in this study we analyzed the histomorphometry of the tibialis anterior muscle (TA) of Wistar rats remobilized using WBV. For the experiment, 32 male Wistar rats were used and divided into four groups (n = 8/group). Groups consisted of: control (CG), immobilized (IG), immobilized and remobilized freely (FG), and immobilized and remobilized with WBV (WG). After the experimental period, the TA was collected and processed for analysis in light microscopy. When compared to the control group, significant morphological changes were observed, which characterize muscle atrophy and reduction of all histomorphometric parameters of the TA of the immobilized animals. Remobilized animals showed improvement in all parameters, and the WBV was not different from the free remobilization, except for the reduction of central nuclei, which can be related to acceleration of the process of tissue regeneration. Thus, we can conclude that the WBV can have an impact on the acceleration of the muscle regenerative process, and may be beneficial in people with reduced mobility.
Background. Due to the deleterious effects of obesity on muscle tissue and the search for tools to reverse these losses, it is important to understand the effect of physical exercises on the muscle structure of obese individuals. This study aimed to analyze the effect of wholebody vibration (WBV) on the histomorphological parameters of the anterior tibial muscle using the monosodium l-glutamate (MSG) obesity model. Methods. MSG-obese rats that were exposed to WBV on a vibrating platform with a frequency of 60 Hz, the amplitude of 2 mm, three times/week, 10 min/day, for eight weeks (from postnatal day (PN) 80 to PN136). The histomorphology of the anterior tibial muscle was evaluated. Results. When performing a WBV exercise, the animals showed altered structural responses in the MSG animals, such as reduced muscle mass, increased connective tissue, and nuclear activity. The WBV reduced the extracellular matrix and the nuclear activity in the MSG animals, showing efficiency in the protocol. Conclusions. Even with the aggressive character of the MSG model, the WBV exercise was able to induce repair to the muscle tissue of these animals, thus being a safe protocol for use in similar conditions.
The model of obesity induced by monosodium glutamate cytotoxicity on the hypothalamic nuclei is widely used in the literature. However, MSG promotes persistent muscle changes and there is a significant lack of studies that seek to elucidate the mechanisms by which damage refractory to reversal is established. This study aimed to investigate the early and chronic effects of MSG in-duction of obesity upon systemic and muscular parameters of Wistar rats. Animals were exposed to MSG subcutaneously (4 mg.g-1 b.w.) or saline (1.25 mg.g-1 b.w.) daily from PND01 to PND05 (n = 24). After, in PND15, 12 animals were euthanized to determine the plasma and inflammatory profile and to assess muscle damage. In PND142, the remaining animals were euthanized, and samples for histological and biochemical analyses were obtained. Our results suggest that early exposure to MSG reduced growth, and increased adiposity, induction hyperinsulinemia, and a pro-inflammatory scenario. In adulthood were found, peripheral insulin resistance, reduced muscle mass, oxidative capacity, neuromuscular junctions, increased fibrosis, and oxidative distress. Thus, we can conclude that the condition found in adult life and the difficulty in restoring the muscle profile are related to the metabolic damages established early.
Our objective was to investigate how metabolic changes, the antioxidant system and the accumulation of oxidative damage occur in muscles with different fibre populations during the ageing process of Wistar rats, as well as to try to map the key age at which these changes occur. For this, 30 male Wistar rats were euthanized aged 11, 15 and 19 months. Then, changes in energy metabolism, antioxidant system and oxidative damage in the soleus and extensor digitorum longus muscles were determined. In this sense, it was possible to observe that changes in body characteristics occur after 15 months of age. Regarding muscle biochemical alterations, we can observe that the soleus muscle presents alterations in protein and anaerobic metabolism only at 19 months, while the extensor digitorum longus presents these alterations at 15 months. Even with the different induction of the antioxidant system between the muscles, the damage accumulation is similar between the two muscles. Therefore, it is possible to conclude that at 15 months of age, the metabolic changes that lead to the reduction of muscle mass and strength found in ageing begin, being, therefore, a key age for the application of interventions that seek to curb the reduction of mass and muscle strength, promoting a better quality of life for individuals.
Estrogen is essential for maintaining the mass and strength of the muscle, and its decrease in menopause leads to sarcopenia. Among the therapeutic modalities, the whole body vibration
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