4.5 Article

Effects of sleeping with reduced carbohydrate availability on acute training responses

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 119, Issue 6, Pages 643-655

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00857.2014

Keywords

cycling; HIT; train low; sleep-low; muscle glycogen

Funding

  1. Sports Nutrition Department of the Australian Institute of Sport
  2. National Sports Institute of Malaysia
  3. European Research Council Ideas Program (ICEBERG) [ERC-2008-AdG23285]
  4. Swedish Research Council
  5. Novo Nordisk Fonden [NNF14OC0011493] Funding Source: researchfish

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We determined the effects of periodized nutrition on skeletal muscle and whole body responses to a bout of prolonged exercise the following morning. Seven cyclists completed two trials receiving isoenergetic diets differing in the timing of ingestion: they consumed either 8 g/kg body mass (BM) of carbohydrate (CHO) before undertaking an evening session of high-intensity training (HIT) and slept without eating (FASTED), or consumed 4 g/kg BM of CHO before HIT, then 4 g/kg BM of CHO before sleeping (FED). The next morning subjects completed 2 h of cycling (120SS) while overnight fasted. Muscle biopsies were taken on day 1 (D1) before and 2 h after HIT and on day 2 (D2) pre-, post-, and 4 h after 120SS. Muscle [glycogen] was higher in FED at all times post-HIT (P < 0.001). The cycling bouts increased PGC1 alpha mRNA and PDK4 mRNA (P < 0.01) in both trials, with PDK4 mRNA being elevated to a greater extent in FASTED (P < 0.05). Resting phosphorylation of AMPK(Thr172), p38MAPK(Thr180/Tyr182), and p-ACC(Ser79) (D2) was greater in FASTED (P < 0.05). Fat oxidation during 120SS was higher in FASTED (P < 0.01), coinciding with increases in ACCSer79 and CPT1 as well as mRNA expression of CD36 and FABP3 (P < 0.05). Methylation on the gene promoter for COX4I1 and FABP3 increased 4 h after 120SS in both trials, whereas methylation of the PPAR delta promoter increased only in FASTED. We provide evidence for shifts in DNA methylation that correspond with inverse changes in transcription for metabolically adaptive genes, although delaying postexercise feeding failed to augment markers of mitochondrial biogenesis.

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