4.6 Article

Leucine-enriched essential amino acid and carbohydrate ingestion following resistance exercise enhances mTOR signaling and protein synthesis in human muscle

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00582.2007

关键词

muscle protein synthesis; mammalian target of rapamycin; essential amino acids

资金

  1. NCRR NIH HHS [M01 RR 00073, M01 RR000073, M01 RR000073-28, S10 RR016650-01, S10 RR 16650] Funding Source: Medline
  2. NIAMS NIH HHS [R01 AR049877, R01 AR 049877, R01 AR049877-05A1] Funding Source: Medline
  3. NIA NIH HHS [P30 AG024832, P30 AG 024832, P30 AG024832-04] Funding Source: Medline
  4. NICHD NIH HHS [T32 HD007539, T32 HD007539-07] Funding Source: Medline
  5. PHS HHS [H133 PO 40003] Funding Source: Medline

向作者/读者索取更多资源

We recently showed that resistance exercise and ingestion of essential amino acids with carbohydrate (EAA + CHO) can independently stimulate mammalian target of rapamycin (mTOR) signaling and muscle protein synthesis in humans. Providing an EAA + CHO solution postexercise can further increase muscle protein synthesis. Therefore, we hypothesized that enhanced mTOR signaling might be responsible for the greater muscle protein synthesis when leucine-enriched EAA + CHOs are ingested during postexercise recovery. Sixteen male subjects were randomized to one of two groups (control or EAA + CHO). The EAA + CHO group ingested the nutrient solution 1 h after resistance exercise. mTOR signaling was assessed by immunoblotting from repeated muscle biopsy samples. Mixed muscle fractional synthetic rate (FSR) was measured using stable isotope techniques. Muscle protein synthesis and 4E-BP1 phosphorylation during exercise were significantly reduced (P < 0.05). Postexercise FSR was elevated above baseline in both groups at 1 h but was even further elevated in the EAA + CHO group at 2 h postexercise (P < 0.05). Increased FSR was associated with enhanced phosphorylation of mTOR and S6K1 (P < 0.05). Akt phosphorylation was elevated at 1 h and returned to baseline by 2 h in the control group, but it remained elevated in the EAA + CHO group (P < 0.05). 4E- BP1 phosphorylation returned to baseline during recovery in control but became elevated when EAA + CHO was ingested (P < 0.05). eEF2 phosphorylation decreased at 1 and 2 h postexercise to a similar extent in both groups (P < 0.05). Our data suggest that enhanced activation of the mTOR signaling pathway is playing a role in the greater synthesis of muscle proteins when resistance exercise is followed by EAA + CHO ingestion.

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