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We hypothesized that the muscle protein anabolic resistance to amino acids occurs in older adults and that RET could overcome such anabolic resistance by enhancing mTORC1 signaling and MPS. To test this hypothesis, we performed the same study but using an isolated muscle sample of 18–20% of the subject's maximum daily amount of protein; thus, not a bodypart with much muscle mass that would affect muscle protein synthesis. Thus, we focused on the elderly group. In order to compare the response of the aging muscle to the acute ingestion of either a 0.3 g/kg (1.3 g) solution or 4.9 g [0.8 g, 1.4 g] of protein/d of carbohydrate, we randomly assigned 22 young male subjects (mean age = 58 ± 2 yrs, body mass = 74.1 ± 5.2 kg, 75% body fat) and 30 older subjects (mean age = 56 ± 4 yrs, body mass = 76.1 ± 5.3 kg, 75% body fat) to an intermittent diet to a protein or a carbohydrate diet. Participants were randomly assigned to the two groups of 2.5 mo each. Subjects ingested two separate meals before a training period with a 60-min rest to determine the timing of food intake. They were then fed 0.3 or 4.9 g [0.8 g, 1.4 g] of protein/d. The amino acid response to the acute ingestion of the carbohydrate and protein formulations was found in the same study [35], [38], while the results regarding the amino acid response to dietary amino acids were the least clear, and hence may be due to differences in the study participants. To identify the amino acid concentrations that would best modulate MPS and muscle protein accretion, we measured the fractional synthetic rate (FSR) on a biopsy obtained from the soleus muscle of young muscle (1 mL) following ingestion of carbohydrate (CHO): 100% of the amount of the previous meal and 50% of the same amount of the next meal and the following day. Two biopsies were taken before (post) and after the exercise protocol to determine the ratio of the time available to accrue muscle protein synthesis and the amount of protein accumulated. The fasting blood amino acid concentrations (MAA concentrations) were measured immediately before exercise and approximately 1.5 h later, using an intraassay value of 2 mg/mL [38], while the post-exercise blood MAA concentrations were determined by measuring the post-exercise serum concentrations of MAA [38]. Data were then analyzed using a software program using the Bio-Rad proprietary software package PSS (http://nim Related Article:
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