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Clinical Trials/NCT03952884
NCT03952884CompletedNot Applicable

Skeletal Muscle Protein Synthetic Response to Amino Acid and Peptides

University of Illinois at Urbana-Champaign1 site in 1 country10 target enrollmentStarted: May 3, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Fractional Synthetic Rate of Myofibrillar Proteins

Study Overview

Brief Summary

Skeletal muscle quality is an important determinant of exercise performance and overall health. It is vital for not just movement, but also metabolizing nutrients. Protein from the diet can promote muscle protein synthesis for muscle recovery and growth. More importantly, doing so shifts net protein balance positively (e.g. protein synthesis is greater than protein breakdown) and promotes greater rates of muscle protein turnover. Leucine is an amino acid required to build muscle, but it also acts as a signaling molecule informing the muscle to start protein synthesis. Before reaching skeletal muscle, dietary protein is digested into small peptides and free amino acids. Rate of absorption from the intestine to the blood stream is significantly faster for peptides compared to amino acids. As amino acid availability in the blood is a precursor for muscle protein synthesis, our objective is to determine if the different absorption rates between free amino acid and peptides influence muscle protein synthetic and breakdown rates.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Recreationally-active adults: ≥ 30 min of physical activity at moderate intensity ≥ 3 times per week
  • •Ages: 18-35 years old
  • •English fluency

Exclusion Criteria

  • •Tobacco, nicotine (patch/gum) use (previous 6 mo)
  • •Alcohol consumption >10 drinks per week
  • •Metabolic disorders (e.g., Metabolic Syndrome, Diabetes, thyroid diseases)
  • •Cardiovascular disease, arrhythmias
  • •Hypogonadism
  • •History of uncontrolled hypertension
  • •Orthopedic injury/surgery (within 1 yr)
  • •Hepatorenal, musculoskeletal, autoimmune, or neurological disease
  • •History of neuromuscular problems
  • •Previous participation in amino acid tracer studies
  • •Predisposition to hypertrophic scarring or keloid formation
  • •Consumption of ergogenic-levels of dietary supplements that may affect muscle mass (e.g., creatine, HMB), insulin-like substances, or anabolic/catabolic pro-hormones (e.g., DHEA) within 6 weeks prior to participation
  • •Consumption of thyroid, androgenic, or other medications known to affect endocrine function
  • •Consumption of medications known to affect protein metabolism (e.g., prescription-strength corticosteroids, non-steroidal anti-inflammatories, or acne medication)
  • •Currently pregnant

Arms & Interventions

Leucine

Active Comparator

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g leucine powder dissolved in 250 mL of water.

Intervention: Resistance Exercise (Behavioral)

Leucine

Active Comparator

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g leucine powder dissolved in 250 mL of water.

Intervention: No Resistance Exercise (Behavioral)

Leucine Peptide (Dileucine)

Experimental

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g protein peptide powder dissolved in 250 mL of water.

Intervention: Resistance Exercise (Behavioral)

Leucine Peptide (Dileucine)

Experimental

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g protein peptide powder dissolved in 250 mL of water.

Intervention: No Resistance Exercise (Behavioral)

Leucine Peptide (Dileucine)

Experimental

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g protein peptide powder dissolved in 250 mL of water.

Intervention: Dileucine (Dietary Supplement)

Leucine

Active Comparator

Participants will be allocated to an exercise or non-exercise group. After resistance exercise (or equivalent time point for non-exercise group), participants will consume 2g leucine powder dissolved in 250 mL of water.

Intervention: Leucine (Dietary Supplement)

Outcomes

Primary Outcomes

Fractional Synthetic Rate of Myofibrillar Proteins

Time Frame: Postabsorptive for 3.5 hours, Postprandial for 3 hours.

Myofibrillar muscle protein synthesis rates will be assessed during the 3.5hr Postabsorptive period (e.g. non-fed state) and the 3hr postprandial period (e.g. fed state) for both experimental interventions (e.g. leucine and leucine peptide). This will allow us to assess the change in fractional synthetic rate from the Postabsorptive period to the postprandial period.

Fractional Synthetic Rate of Mixed Muscle Proteins

Time Frame: Postabsorptive for 3.5 hours, Postprandial for 3 hours.

Mixed muscle protein synthesis rates will be assessed during the 3.5hr Postabsorptive period (e.g. non-fed state) and the 3hr postprandial period (e.g. fed state) for both experimental interventions (e.g. leucine and leucine peptide). This will allow us to assess the change in fractional synthetic rate from the Postabsorptive period to the postprandial period.

Fractional Breakdown Rate of Mixed Muscle Proteins

Time Frame: Postprandial for 1 hour

Mixed muscle protein breakdown rates will be assessed during the first hour of the postprandial period (e.g. fed state) for both experimental interventions (e.g. leucine and leucine peptide). This will allow us to assess the change in fractional breakdown rate for each respective experimental intervention.

Secondary Outcomes

  • Phosphorylation of muscle anabolic signaling(Baseline, immediately after ingestion of leucine/leucine peptides, and 3 hours after ingestion of leucine/leucine peptides)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nicholas Burd

Assistant Professor

University of Illinois at Urbana-Champaign

Study Sites (1)

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