1,644 research outputs found

    THE EFFECTS OF EXTERNAL LOAD ON LOWER EXTREMiTY ELECTROMYOGRAPHY AMPLITUDE DURING COUNTERMOVEMENT JUMP

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    The purpose of this study was to investigate the effects of different loads on the mean electromyography (EMG) amplitude of the gluteus maximus, biceps fernoris, vastus medialis, gastrocnemius, soleus, and tibialis anterior during the deceleration phase and the acceleration phase of the countermovement jumps (CMJ). Ten male physical education students performed different CMJs with and without an external load (0,2.5,5.0, 7.5, or 10.0 kg hold in arms). The results s h o w the amplitude of the gluteus maximus with load of 7.5 kg was higher than with load of 2.5 kg during the deceleration phase (p < .05), and the amplitude of the soleus with load of 10.0 kg was higher than with load of 2.5 kg during the acceleration phase (p < .05). It indicated that the activities of lower limb muscles were not influenced by the relative lower of external loading during CMJ

    Direct effects of caffeine on osteoblastic cells metabolism: the possible causal effect of caffeine on the formation of osteoporosis

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    BACKGROUND: Caffeine consumption has been reported to decrease bone mineral density (BMD), increase the risk of hip fracture, and negatively influence calcium retention. In this study, we investigated the influence of caffeine on the osteoblasts behaviour. METHOD: Osteoblasts derived from newborn Wistar-rat calvaria was used in this study. The effects of various concentrations of caffeine on bone cell activities were evaluated by using MTT assay. Alkaline phosphatase (ALP) staining, von Kossa staining and biochemical parameters including ALP, lactate dehydrogenase (LDH), prostaglandin E(2 )(PGE(2)) and total protein were performed at day 1, 3, and 7. DNA degradation analysis under the caffeine influence was also performed. RESULTS AND DISCUSSION: The results showed that the viability of the osteoblasts, the formation of ALP positive staining colonies and mineralization nodules formation in the osteoblasts cultures decreased significantly in the presence of 10 mM caffeine. The intracellular LDH, ALP and PGE(2 )content decreased significantly, the LDH and PGE(2 )secreted into the medium increased significantly. The activation of an irreversible commitment to cell death by caffeine was clearly demonstrated by DNA ladder staining. CONCLUSION: In summary, our results suggest that caffeine has potential deleterious effect on the osteoblasts viability, which may enhance the rate of osteoblasts apoptosis
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