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1.
Braz. j. med. biol. res ; 44(6): 546-552, June 2011. ilus
Article Dans Anglais | LILACS | ID: lil-589974

Résumé

Our objective was to determine lipid peroxidation and nuclear factor-κB (NF-κB) activation in skeletal muscle and the plasma cytokine profile following maximum progressive swimming. Adult male Swiss mice (N = 15) adapted to the aquatic environment were randomly divided into three groups: immediately after exercise (EX1), 3 h after exercise (EX2) and control. Animals from the exercising groups swam until exhaustion, with an initial workload of 2 percent of body mass attached to the tail. Control mice did not perform any exercise but were kept immersed in water for 20 min. Maximum swimming led to reactive oxygen species (ROS) generation in skeletal muscle, as indicated by increased thiobarbituric acid reactive species (TBARS) levels (4062.67 ± 1487.10 vs 19,072.48 ± 8738.16 nmol malondialdehyde (MDA)/mg protein, control vs EX1). Exercise also promoted NF-κB activation in soleus muscle. Cytokine secretion following exercise was marked by increased plasma interleukin-6 (IL-6) levels 3 h post-exercise (P < 0.05). Interleukin-10 (IL-10) levels were reduced following exercise and remained reduced 3 h post-exercise (P < 0.05). Plasma levels of other cytokines investigated, monocyte chemotactic protein-1 (MCP-1), tumor necrosis factor-alpha (TNF-α), interferon-gamma (IFN-γ) and interleukin-12 (IL-12), were not altered by exercise. The present findings showed that maximum swimming, as well as other exercise models, led to lipid peroxidation and NF-κB activation in skeletal muscle and increased plasma IL-6 levels. The plasma cytokine response was also marked by reduced IL-10 levels. These results were attributed to exercise type and intensity.


Sujets)
Animaux , Mâle , Souris , Cytokines/sang , Peroxydation lipidique/physiologie , Muscles squelettiques/métabolisme , Facteur de transcription NF-kappa B/métabolisme , Natation/physiologie , Indice de masse corporelle , /sang , /sang , /sang , Malonaldéhyde/métabolisme , Conditionnement physique d'animal/physiologie , Répartition aléatoire , Espèces réactives de l'oxygène/métabolisme , Facteurs temps , Substances réactives à l'acide thiobarbiturique/métabolisme
2.
Braz. j. med. biol. res ; 28(6): 705-9, Jun. 1995. tab
Article Dans Anglais | LILACS | ID: lil-154942

Résumé

Stimulant properties during exercise have been attributed to cafeine (CAF) and tryptophan (Trp). The purpose of the present study was to investigate the effects of CAF and Trp ingestion on rectal temperature (Tre), total exercise time (TET), oxygen consumption (VO2), carbon dioxide production (VCO2) pulmunary ventilation (VE), heart rate (HR) and rate of perceived exertion (RPE) during exercise on a cycle ergometer at 80 percent of maximal work load, in eight halthy male volunteers. Each subject abstained from caffeine for 48 h and from animal-derived foods for 36 h before each experiment. Aerobic capacity was determined on the first day. In consecutive trials, conducted in a double-blind, randomized, crossed-over manner, each subject recived capsules containing CAF (10mg/Kg), Trp (1.2g), a combination of the two (CAF + TRP), and lactose (PLA), 1 h before exercise. Plasma CAF concentration (PC) was measured by high performance liquid chromatography (HPLC), before (basal concentration) and 1 and 2 h after ingestion of the capsules. At both times after CAF or CAF + Trp ingestion, the PC was elevated compared with the basal concentration (P < 0.05). During exercise, significant increases occured with time in Tre, TET, VO2, VCO2, VE, HR and RPE (P < 0.01) while no significant difference was observed when CAF or CAF+ Trp were compared with control values. Under the conditions of this study, CAF and/or Trp did not affect the physiological parameters measured before, during or after exercise at 80 percent of maximal work load


Sujets)
Humains , Mâle , Adulte , Température du corps/effets des médicaments et des substances chimiques , Caféine/administration et posologie , Consommation d'oxygène , Exercice physique/physiologie , Rythme cardiaque , Tryptophane/administration et posologie
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