Changes in oxidative stress, inflammation and muscle damage markers following eccentric versus concentric cycling in older adults

European Journal of Applied Physiology(2019)

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摘要
Purpose To compare concentric and eccentric cycling performed by older adults for metabolic demand and post-exercise oxidative stress, inflammation and muscle damage. Methods Eight male and two female healthy older adults (60.4 ± 6.8 years) performed 30 min of moderate-intensity concentric (CONC-M: 50% maximum power output; PO max ) and eccentric cycling (ECC-M: 50% PO max ) and high-intensity eccentric cycling (ECC-H: 100% PO max ) in a randomized order. Average power output (PO), oxygen consumption ( V O 2 ), heart rate (HR) and rate of perceived exertion were recorded during cycling. Some indirect markers of muscle damage were assessed before, and immediately, 24 and 48 h after cycling. Markers of oxidative stress (malondialdehyde: MDA, protein carbonyl), antioxidant (total antioxidant capacity, glutathione peroxidase activity: GPx) and inflammation (IL-6, TNF-α) were measured before and 5 min after cycling. Results PO in ECC-H (202.6 ± 78.5 W) was > 50% greater ( P < 0.05) than that of CONC-M (98.6 ± 33.1 W) and ECC-M (112.0 ± 42.1 W). V O 2 and HR were also greater ( P < 0.05) for ECC-H than CONC-M (50% and 17%, respectively) and ECC-M (40% and 23%, respectively). Muscle strength loss at 1 day post-exercise (8–22%), peak soreness (10–62 mm) and creatine kinase activity (30–250 IU/L) after ECC-H were greater ( P < 0.05) than those after ECC-M and CONC-M. MDA decreased ( P < 0.05) after CONC-M (− 28%) and ECC-M (− 22%), but not after ECC-H. GPx activity increased after all exercises similarly (20–27%). IL-6 increased ( P < 0.05) only after ECC-H (18%). Conclusion Oxidative stress was minimal after eccentric cycling, but high-intensity eccentric cycling induced moderate muscle damage and inflammation, which is not desirable for older individuals.
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关键词
Lengthening muscle action, Muscle soreness, Creatine kinase, TNF alpha, TBARS, Total antioxidant capacity, Interleukin 6
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