4.6 Article

Similar Expression of Oxidative Genes after Interval and Continuous Exercise

期刊

MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
卷 41, 期 12, 页码 2136-2144

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1249/MSS.0b013e3181abc1ec

关键词

BIOMARKERS; INTERVAL TRAINING; METABOLIC ADAPTATION; MUSCLE OXIDATIVE POTENTIAL; TRANSCRIPTIONAL REGULATION

资金

  1. Swedish Research Council [20654]
  2. National Centre for Research in Sport
  3. Swedish School of Sport and Health Sciences (GIH)
  4. Chinese PhD Program Scholarship Fund of ECNU 2007
  5. National Institutes of Health
  6. Wellcome Trust
  7. Howard Hughes Medical Institute

向作者/读者索取更多资源

WANG, L., N. PSILANDER, M. TONKONOGI, S. DING, and K. SAHLIN. Similar Expression of Oxidative Genes after Interval and Continuous Exercise. Med. Sci. Sports Exerc., Vol. 41, No. 12 pp. 2136-2144, 2009. Purpose: There is a debate whether interval or traditional endurance training is the most effective Stimulus of mitochondrial biogenesis. Here, we compared the effects of acute interval exercise (IE) or continuous exercise (CE) on the muscle messenger RNA (mRNA) content for several genes involved in mitochondrial biogenesis and lipid metabolism. Methods: Nine sedentary subjects cycled for 90 min with two protocols: CE (at 67% (V) over dotO(2max)) and IE (12 s at 120% and 18 s at 20% of (V) over dotO(2max)). The duration of exercise and work performed with CE and IE was identical. Muscle biopsies were taken before and 3 h after exercise. Results: There were no significant differences between the two exercise protocols in the increases in (V) over dotO(2) and HR, the reduction in muscle glycogen (35%-40% with both protocols) or the changes in blood metabolites (lactate, glucose, and fatty acids), The mRNA content for major regulators of mitochondrial biogenesis [peroxisome proliferator-activated receptor (PPAR) gamma coactivator 1 alpha (PGC-1 alpha), PGC-1-related coactivator, PPAR beta/delta] and of lipid metabolism [pyruvate dehydrogenase kinase isozyme 4 (PDK4)] increased after exercise, but there was no significant difference between IE and CE. However, the mRNA content for several downstream targets of PGC-1 alpha increased significantly only after CE, and mRNA content for nuclear respiratory factor 2 was significantly higher after CE (P < 0.025 vs IE). Conclusions: The present findings demonstrate that, when the duration of exercise and work performed is the same, IE and CE influence the transcription of genes involved in oxidative metabolism in a similar manner.

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