233 resultados para soleus


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The aim of this study was to verify the effects of running overtraining protocols performed in downhill, uphill, and without inclination on the proteins related to hypertrophy signaling pathway in extensor digitorum longus (EDL) and soleus of C57BL/6 mice. We also performed histological and stereological analyses. Rodents were divided into control (CT; sedentary mice), overtrained by downhill running (OTR/down), overtrained by uphill running (OTR/up), and overtrained by running without inclination (OTR). The incremental load, exhaustive, and grip force tests were used as performance evaluation parameters. 36 h after the grip force test, EDL and soleus were removed and immediately used for immunoblotting analysis or stored at -80°C for histological and stereological analyses. For EDL, OTR/down decreased the protein kinase B (Akt) and tuberous sclerosis protein 2 (TSC2) phosphorylation (p), and increased myostatin, receptor-activated Smads (pSMAD2-3), and insulin receptor substrate-1 (pIRS-1; Ser307/636). OTR/down also presented low and high relative proportions of cytoplasm and connective tissue, respectively. OTR/up increased the mammalian target of rapamycin (pmTOR), 70-kDa ribosomal protein S6 kinase 1 (pS6K1) and pSMAD2-3, and decreased pTSC2. OTR decreased pTSC2 and increased pIRS-1 (Ser636). For soleus, OTR/down increased S6 ribosomal protein (pS6RP) and pSMAD2-3, and decreased pIRS-1 (Ser639). OTR/up decreased pS6K1, pS6RP and pIRS-1 (Ser639), and increased pTSC2 (Ser939), and pSMAD2-3. OTR increased pS6RP, 4E-binding protein-1 (p4E-BP1), pTSC2 (Ser939), and pSMAD2-3, and decreased pIRS-1 (Ser639). In summary, OTR/down inhibited the skeletal muscle hypertrophy with concomitant signs of atrophy in EDL. The effects of OTR/up and OTR depended on the analyzed skeletal muscle type. J. Cell. Physiol. 9999: 1-12, 2015. © 2015 Wiley Periodicals, Inc.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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A perda de massa muscular observada no diabetes mellitus (DM) tipo 1 é consequência da combinação entre redução na velocidade de síntese proteica e aumento na velocidade de proteólise. A curcumina, pigmento amarelo extraído dos rizomas de Curcuma longa L., promove diversos benefícios no metabolismo de carboidratos e lipídeos no DM. Deste modo, buscamos avaliar o efeito do tratamento de ratos diabéticos com curcumina incorporada em iogurte sobre o metabolismo proteico muscular. Ratos Wistar machos (150±10 g) receberam estreptozotocina (40 mg/kg, i.v.) para indução do DM e foram divididos nos grupos (n=8): diabético tratado com iogurte (DIOG), 90 mg/kg de curcumina (DC90), 4U de insulina (DINS) e ratos normais, não diabéticos, tratados com iogurte (NIOG). Após 35 dias de tratamento, os animais foram eutanasiados e os músculos esqueléticos soleus e extensor digitorium longus (EDL) foram retirados e utilizados para a determinação das atividades proteolíticas de caspase-3, calpaína e proteassoma (atividade quimiotripsina-like). O tratamento de animais diabéticos com curcumina incorporada em iogurte reduziu a glicemia, os níveis de ureia urinária e promoveu um maior ganho de peso corporal em relação aos animais diabéticos tratados somente com iogurte (DIOG). Animais DIOG apresentaram um aumento nas atividades de calpaína e proteassoma em músculos soleus e EDL em relação aos valores encontrados em músculos de animais NIOG; já o tratamento com curcumina reduziu as atividades de calpaína e proteassoma em EDL de ratos diabéticos, o que explica, pelo menos em parte, a menor perda de massa deste músculo em ratos DC90. Houve uma redução na atividade de caspase-3 em músculos de animais DIOG em comparação aos grupos...

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A perda de massa muscular observada no diabetes mellitus (DM) tipo 1 é consequência da combinação entre redução na velocidade de síntese proteica e aumento na velocidade de proteólise. A curcumina, pigmento amarelo extraído dos rizomas de Curcuma longa L., promove diversos benefícios no metabolismo de carboidratos e lipídeos no DM. Deste modo, buscamos avaliar o efeito do tratamento de ratos diabéticos com curcumina incorporada em iogurte sobre o metabolismo proteico muscular. Ratos Wistar machos (150±10 g) receberam estreptozotocina (40 mg/kg, i.v.) para indução do DM e foram divididos nos grupos (n=8): diabético tratado com iogurte (DIOG), 90 mg/kg de curcumina (DC90), 4U de insulina (DINS) e ratos normais, não diabéticos, tratados com iogurte (NIOG). Após 35 dias de tratamento, os animais foram eutanasiados e os músculos esqueléticos soleus e extensor digitorium longus (EDL) foram retirados e utilizados para a determinação das atividades proteolíticas de caspase-3, calpaína e proteassoma (atividade quimiotripsina-like). O tratamento de animais diabéticos com curcumina incorporada em iogurte reduziu a glicemia, os níveis de ureia urinária e promoveu um maior ganho de peso corporal em relação aos animais diabéticos tratados somente com iogurte (DIOG). Animais DIOG apresentaram um aumento nas atividades de calpaína e proteassoma em músculos soleus e EDL em relação aos valores encontrados em músculos de animais NIOG; já o tratamento com curcumina reduziu as atividades de calpaína e proteassoma em EDL de ratos diabéticos, o que explica, pelo menos em parte, a menor perda de massa deste músculo em ratos DC90. Houve uma redução na atividade de caspase-3 em músculos de animais DIOG em comparação aos grupos...

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High consumption of polyunsaturated fatty acids, such as sunflower oil has been associated to beneficial effects in plasma lipid profile, but its role on inflammation and insulin resistance is not fully elucidated yet. We evaluated the effect of sunflower oil supplementation on inflammatory state and insulin resistance condition in HFD-induced obese mice. C57BL/ 6 male mice (8 weeks) were divided in four groups: (a) control diet (CD), (b) HFD, (c) CD supplemented with n-6 (CD + n-6), and (d) HFD supplemented with n-6 (HFD + n-6). CD + n-6 and HFD + n-6 were supplemented with sunflower oil by oral gavage at 2 g/ Kg of body weight, three times per week. CD and HFD were supplemented with water instead at the same dose. HFD induced whole andmuscle-specific insulin resistance associated with increased inflammatory markers in insulin-sensitive tissues andmacrophage cells. Sunflower oil supplementation was not efficient in preventing or reducing these parameters. In addition, the supplementation increased pro-inflammatory cytokine production by macrophages and tissues. Lipid profile, on the other hand, was improved with the sunflower oil supplementation in animals fed HFD. In conclusion, sunflower oil supplementation improves lipid profile, but it does not prevent or attenuate insulin resistance and inflammation induced by HFD in C57BL/ 6 mice.

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The effect of short-term creatine (Cr) supplementation upon content of skeletal muscle-derived-reactive oxygen species (ROS) was investigated. Wistar rats were supplemented with Cr (5 g/kg BW) or vehicle, by gavage, for 6 days. Soleus and extensor digitorum longus (EDL) muscles were removed and incubated for evaluation of ROS content using Amplex-UltraRed reagent. The analysis of expression and activity of antioxidant enzymes (superoxide dismutase 1 and 2, catalase and glutathione peroxidase) were performed. Direct scavenger action of Cr on superoxide radical and hydrogen peroxide was also investigated. Short-term Cr supplementation attenuated ROS content in both soleus and EDL muscles (by 41 and 33.7%, respectively). Cr supplementation did not change expression and activity of antioxidant enzymes. Basal TBARS content was not altered by Cr supplementation. In cell-free experiments, Cr showed a scavenger effect on superoxide radical in concentrations of 20 and 40 mM, but not on hydrogen peroxide. These results indicate that Cr supplementation decreases ROS content in skeletal muscle possibly due to a direct action of Cr molecule on superoxide radical.

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beta(2)-adrenergic receptor (beta(2)-AR) agonists have been used as ergogenics by athletes involved in training for strength and power in order to increase the muscle mass. Even though anabolic effects of beta(2)-AR activation are highly recognized, less is known about the impact of beta(2)-AR in endurance capacity. We presently used mice lacking beta(2)-AR [beta(2)-knockout (beta(2) KO)] to investigate the role of beta(2)-AR on exercise capacity and skeletal muscle metabolism and phenotype. beta(2) KO mice and their wild-type controls (WT) were studied. Exercise tolerance, skeletal muscle fiber typing, capillary-to-fiber ratio, citrate synthase activity and glycogen content were evaluated. When compared with WT, beta 2KO mice displayed increased exercise capacity (61%) associated with higher percentage of oxidative fibers (21% and 129% of increase in soleus and plantaris muscles, respectively) and capillarity (31% and 20% of increase in soleus and plantaris muscles, respectively). In addition, beta 2KO mice presented increased skeletal muscle citrate synthase activity (10%) and succinate dehydrogenase staining. Likewise, glycogen content (53%) and periodic acid-Schiff staining (glycogen staining) were also increased in beta 2KO skeletal muscle. Altogether, these data provide evidence that disruption of beta(2)AR improves oxidative metabolism in skeletal muscle of beta 2KO mice and this is associated with increased exercise capacity.

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The objective was to determine the effects of carbohydrate (CHO) supplementation on exercise-induced hormone responses and post-training intramyocellular lipid stores (IMCL). Twenty-four elite male athletes (28.0 +/- 1.2 years) were randomized to receive CHO (maltodextrin solution) or zero energy placebo solution (control group). The high-intensity running protocol consisted of 10 x 800 m at 100% of the best 3000-m speed (Vm3 km) and 2 x 1000 m maximal bouts in the morning and a submaximal 10-km continuous easy running in the afternoon of day 9. IMCL concentrations were assessed by H-1-MRS before (-day 9) and after training (day 9) in soleus (SO) and tibialis anterior (TA) muscles. Blood hormones were also measured before, during, and post-exercise. The percent change (Delta%) in TA-IMCL was higher in the CHO group (47.9 +/- 24.5 IMCL/Cr) than in the control group (-1.7 +/- 13.1, respectively) (P=.04). Insulin concentrations were higher in the CHO group post-intermittent running compared to control (P=.02). Circulating levels of free fatty acids and GH were lower in the CHO group (P>.01). The decline in performance in the 2nd 1000-m bout was also attenuated in this group compared to control (P<.001 and P=.0035, respectively). The hormonal milieu (higher insulin and lower GH levels) in the CHO group, together with unchanged free fatty acid levels, probably contributed to the increased IMCL stores. This greater energy storage capacity may have improved post-exercise recovery and thus prevented performance deterioration. (C) 2012 Elsevier Inc. All rights reserved.