muscle anabolism
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male • Healthy and physically active (as determined by medical and activity questionnaire) • 20-30 years of age • Having given informed consent
Exclusion criteria
Exclusion criteria: • Having any identified metabolic or intestinal disorders • Tobacco use • Aspirin use in the 4 days prior to the experimental trial • Consumption of prescription medications or any performance enhancing agent • Inability to endure the strenuous exercise bouts e.g. injuries • Alcohol intake during the 48 hours prior to each of the testing days • Currently participating or having participated in another clinical trial during the last 4 weeks prior to the beginning of this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study endpoint is the fractional synthetic rate (FSR) of muscle protein synthesis (mixed, myofibrillar, and mitochondrial proteins) from 0-6 hours in the post-prandial period. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include: • The fractional synthetic rate (FSR) of muscle protein synthesis (mixed, myofibrillar, and mitochondrial proteins) from 0-2 and 2-6 hours in the post-prandial period. • Plasma free phenylalanine enrichment (expressed as MPE) • Plasma free tyrosine enrichment (expressed as MPE) • Plasma total phenylalanine (expressed as µmol/L) • Plasma total tyrosine (expressed as µmol/L) • Total plasma amino acids (AAmax [µmol/L]) • Plasma glucose (glucosemax [mmol/L]) • Plasma insulin (insulinmax [mU/L]) | — |
Countries
Netherlands