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1.
Cell Mol Biol (Noisy-le-grand) ; 63(7): 76-83, 2017 08 15.
Artigo em Inglês | MEDLINE | ID: mdl-28838344

RESUMO

Exercise-induced muscle damage (EIMD) is accompanied by inflammatory and immune responses. However, due to the repeated bout effect, there will probably be less EIMD. Hence, the purpose was to investigate inflammatory and immune responses over a three-day period of downhill running in active females. Eleven moderately trained healthy females performed three 60-minute bouts of downhill running in -13.5% grade, separated by 24 hours, at a speed eliciting 70-80% of their VO2peak on level grade. Delayed onset muscle soreness (DOMS), range of motion (ROM) and maximum knee isotonic strength (1RM) were measured pre- and two-hour post every bout. Blood variables, including CBC, serum lactate dehydrogenase (LDH), creatine kinase (CK), myoglobin (Mb), IL-10, IL-6 and Monocyte chemoattractant protein-1 (MCP-1) were measured at 1 hour before the first bout and two hours after every bout. Data was analysed by repeated measure ANOVA (P<0.05). Although CK, LDH, Mb, IL-10, IL-6, MCP-1, total leukocyte count, monocytes and neutrophils increased significantly following the first bout, CK, LDH, Mb, IL-10, monocytes and neutrophils were only significantly higher following the third bout compared to the baseline (all P<0.05). Moreover, IL-10 and IL-6 decreased following the second and third bouts compared to the first bout (P<0.05). In comparison with the baseline, lymphocytes decreased after the second bout, DOMS increased following the second and third bouts, 1RM decreased following the first and second bouts (all P<0.05). ROM showed no significant difference. The three-day period of downhill running did not exacerbate EIMD and inflammatory response was partly attenuated.


Assuntos
Imunidade , Inflamação/patologia , Corrida/fisiologia , Adulto , Contagem de Células Sanguíneas , Creatina Quinase/sangue , Citocinas/sangue , Feminino , Frequência Cardíaca/fisiologia , Humanos , Inflamação/sangue , L-Lactato Desidrogenase/sangue , Fadiga Muscular/fisiologia , Mioglobina/sangue
2.
Cell Mol Biol (Noisy-le-grand) ; 63(5): 11-18, 2017 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-28719339

RESUMO

Diabetes is known to alter both oxidative and glycolytic pathways in a fiber type-dependent manner. The aim of present study was to investigate the effects of endurance training on muscle NHE1 and NBC1 genes and proteins expression in type 2 diabetic rats. Male wistar rats (n=30), 4 weeks old and 95.7±10.8g, were randomly selected and divided into control, diabetic without training and diabetic with training groups. Diabetes was induced by injection of low dose of streptotozin and feeding with high-fat diet. The Endurance training was performed for 7 weeks that started with relatively low speed and duration of 20 m min-1 for 20 min in the first week and gradually reached to 30 m min-1 for 35min in the last week. NHE1 and NBC1 genes and proteins expression were determined by Real time-PCR and western blotting techniques, respectively, in Soleus as an oxidative and EDL (Extensor digitorum longus) as a glycolytic muscle preparation. NHE1 mRNA and protein expression reduced significantly in EDL and Soleus in the diabetic without training group compared with the control group. However, reduction in the expression of NBC1 gene and protein in the diabetic without training group compared to controls did not significant. Endurance training increased NHE1 and NBC1 genes and proteins expression in both EDL and Soleus in the diabetic training group compared to control groups. In conclusion, endurance training may improve the capacity of pHi regulation in muscles by lactate-independent pathway.


Assuntos
Diabetes Mellitus Experimental/genética , Dieta Hiperlipídica , Regulação da Expressão Gênica , Glicólise , Fibras Musculares de Contração Rápida/metabolismo , Simportadores de Sódio-Bicarbonato/genética , Trocador 1 de Sódio-Hidrogênio/genética , Animais , Biomarcadores/metabolismo , Glicemia/metabolismo , Peso Corporal , Glicólise/genética , Insulina/sangue , Resistência à Insulina , Masculino , Oxirredução , Condicionamento Físico Animal , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ratos Wistar , Simportadores de Sódio-Bicarbonato/metabolismo , Trocador 1 de Sódio-Hidrogênio/metabolismo , Estreptozocina
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