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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03117127
Other study ID # 15693
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date May 2017

Study information

Verified date April 2018
Source University of Illinois at Urbana-Champaign
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In crossover trials, ten (N=10) young men (18-35 y) will receive stable isotope tracer infusions and perform a single bout of resistance exercise. Immediately after resistance exercise, participants will ingest stable isotope labeled whole eggs (18 g protein, 17 g fat) or egg whites (18 g protein, 0 g fat) cooked in scrambled form. Repeated blood and muscle biopsies will be collected to determine whole body amino acid kinetics, muscle amino acid transporters, anabolic signaling and myofibrillar protein synthesis rates during the trials.


Description:

On both infusion trials, participants will report to the laboratory at 0700 h after an overnight fast. Upon arrival to the lab, a baseline breath sample will be collected for determination of 13CO2 enrichment by isotope ratio mass spectrometry. A Teflon catheter will be inserted into an antecubital vein for baseline blood sample collection (t=-210 min) and then participants will receive priming doses of NaH13CO2 (2.35 µmol·kg-1), L-[1-13C]leucine (7.6 µmol·kg-1), and L-[ring-2H5]phenylalanine (2.0 µmol·kg-1). Subsequently, a continuous intravenous infusion of L-[1-13C]leucine (0.10 µmol·kg-1·min-1) and L-[ring-2H5]phenylalanine (0.05 µmol·kg-1·min-1) will be initiated (t=-210 min) and maintained over the infusion trials. A second Teflon catheter willinserted into a heated dorsal hand vein for repeated arterialized blood sampling and remained patent by a 0.9% saline drip. Breath samples and arterialized blood samples and will be collected every 30 or 60 min during the postabsorptive- and postprandial states. In the post-absorptive state of infusion trial 1, muscle biopsies will be collected at t=-150 and -30 min of infusion to determine basal-state myofibrillar protein synthesis rates, relative skeletal muscle amino acid transporter content, and anabolic-related signaling. In the subsequent cross-over trial only 1 muscle biopsy will be collected at t=-30 for Western blot analysis and postabsorptive myofibrillar protein-bound tracer enrichment. After collection of the resting muscle biopsy at t=-30 for both trials, the participants will perform resistance exercise that consists of 4 sets of 10 repetitions at 80% of 10-RM for both leg press and leg extension exercise.

Immediately after completion of the exercise bout, participants will consume 3 whole eggs or an equivalent amount of protein from egg whites (t=0 min). Completion of the meal will mark the start of the postprandial phase (t=0 min) and additional muscle biopsies will be collected at t=120 and 300 min.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date May 2017
Est. primary completion date February 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Male

- Aged 18-35 years

- Healthy, active (self-reported to exercise 2 - 4 times per week)

- BMI > 18.5 and < 25 kg/m2

Exclusion Criteria:

- Smoking

- Known allergies to egg consumption

- Vegans

- Diagnosed GI tract diseases

- Arthritic conditions

- A history of neuromuscular problems

- Diagnosed cognitive impairments

- Recent (1 year) participation in amino acid tracer studies

- Predisposition to hypertrophic scarring or keloid formation

- Individuals on any medications known to affect protein metabolism (i.e. corticosteroids, non-steroidal anti-inflammatories, or prescription strength acne medications).

- High blood pressure (Systolic > 140 mm HG; Diastolic > 90 mm HG)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Resistance Exercise
Participants will perform leg extension and leg press immediately prior to ingestion of whole eggs or egg whites
Other:
Whole Eggs
Participants will ingestion whole eggs immediately after resistance exercise
Egg Whites
Participants will ingestion whole eggs immediately after resistance exercise

Locations

Country Name City State
United States Freer Hall Urbana Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Urbana-Champaign

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional synthetic rate of myofibrillar proteins to whole egg and egg white ingestion Myofibrillar protein synthesis rates will be assessed during the postabsorptive period for 3 hr and during the 5 hr after the ingestion of the experimental beverages. This will allow us to assess the change from the postabsorptive to the postprandial period Postabsorptive for 3 hours, Postprandial for 5 hours
Secondary Phosphorylation of muscle anabolic signaling Phosphorylation of anabolic signaling pathways will be assessed in the fasted state and at 2 and 5 hr after the ingestion of the whole egg and egg whites Baseline and at 2 and 5 hours after protein ingestion
Secondary Exogenous rate of leucine appearance after ingestion of whole eggs and egg whites. Dietary derived leucine availability will be measured during the 5 h postprandial phase to compare the dietary-derived leucine availability after whole egg and egg white ingestion. 5 hour postprandial phase
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