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Olympic class sailing is a competitive sport and requires several abilities. An understanding of the responses to aerobic and anaerobic loading will be useful for assessing the training programs, protective strategies and possibility of injuries. Therefore, the aim of this study is to determine lower extremity main muscles skin temperature responses to aerobic and anaerobic test conditions in Turkish Olympic Sailing Athletes. Eighteen sailing athletes were assessed during preseasonal assessment period. Temperatures of quadriceps and hamstring muscle groups were evaluated bilaterally during rest and after Wingate Treadmill tests. Wingate test was accepted as an indicator of anaerobic performance and Treadmill test as an aerobic performance. Infrared thermography was performed to assess the skin temperature at anterior and posterior parts of thigh for both legs. In the triplicate comparison, the temperature changes between the rest, aerobic test and anaerobic test conditions were significant (p?<?0.05). In the analysis to determine the difference between the compared groups; for both muscle groups, temperature change after anaerobic performance was not significant; in contrast to this result the change in muscle temperature after aerobic performance was significant (p?<?0.05). Energetic—metabolic activity of major muscle groups of lower extremities during aerobic and anaerobic performance are important for injury prevention, treatment, rehabilitation and return to play. Present study shows that aerobic performance or activities requires higher energetic-metabolic activity.
相似文献The selective determination of dopamine (DA) was performed using a glassy carbon (GC) electrode modified with N-(1-H-indole-3yl) methylene thiazole-2-amine (IMT2A). IMT2A was deposited on the GC electrode by cyclic voltammetry. This modified electrode demonstrated an electrocatalytic effect on the oxidation of DA in the presence of uric acid (UA) and ascorbic acid (AA) using differential pulse voltammetry (DPV) method in 0.1 M phosphate buffer solution (PBS) of pH 7. Selective determination was realized in elimination of AA response on the IMT2A-modified electrode. The oxidation peak currents increased linearly with two concentration intervals of DA at pH 7 phosphate buffer. One of them is 0.25–9.15 μM, and the other is 9.15–95.1 μM. The limit of detection (LOD) was found as 0.086 μM. The proposed electrode was applied to the determination of DA in pharmaceutical preparations and human urine sample with satisfactory results.
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