- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04121689
Time Course of Postprandial Protein Metabolism
October 7, 2019 updated by: University of Illinois at Urbana-Champaign
Time-dependent Regulation of Postprandial Muscle Protein Synthesis After Milk Protein Ingestion in Young Men
The anabolic action of 'fast' whey protein on the regulation of postprandial muscle protein synthesis has been established to be short-lived in healthy young adults.
Our aim was assess the time course of anabolic signaling events and stimulation of muscle protein synthesis rates (MPS) after ingestion of a food source that represents a more typical meal-induced pattern of aminoacidemia, namely milk protein concentrate, in healthy young males.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
7
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Urbana, Illinois, United States, 61801
- Freer Hall
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion criteria
- Males
- Aged between 18-35 years
- Healthy, recreationally active
- BMI < 30 kg/m2
Exclusion criteria
- Smoking
- Allergies to milk proteins
- Vegetarians
- Diagnosed GI tract diseases
- Female
- Arthritic conditions
- A history of neuromuscular problems
- Previous 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).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Milk Protein Concentrate
Seven young men (age: 22±1 y) will undergo repeated blood and biopsy sampling during primed continuous L-[ring-2H5]phenylalanine and L-[1-13C]leucine tracer infusions, and ingested 38 g of L-[1-13C]phenylalanine- and L-[1-13C]leucine-labeled milk protein concentrate
|
The macronutrient composition and energy of the milk protein beverage provided to participants is 38 g protein (3.46 g leucine), 4.17 g carbohydrate, and 1.4 g fat.
The milk protein met all chemical and bacteriologic specifications for human consumption.
The L-[1-13C]phenylalanine and L-[1-13C]leucine enrichments in the milk protein concentrate averaged 38.3 and 10.8 mole percent excess (MPE), respectively.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Fractional synthesis rates of myofibrillar protein
Time Frame: 8 hours
|
Myofibrillar protein synthesis rates will be assessed during the postabsorptive period for 3 hours, and every 1-2 hours during the 5 hours after protein ingestion.
This will allow us assess the timecourse of muscle protein synthesis after eating.
|
8 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Phosphorylation of muscle anabolic signaling
Time Frame: 8 hours
|
Phosphorylation of anabolic signaling pathways (mTORC1, AKT, and P70S6K) involved in the stimulation of myofibrillar protein synthesis rates will be assessed during the postabsorptive period for 3 hours, and every 1-2 hours during the 5 hours after protein ingestion.
|
8 hours
|
Exogenous rate of phenylalanine appearance
Time Frame: 5 hours
|
Dietary derived phenylalanine availability will be measured during the 5 h postprandial phase to determine its relationship with the fractional synthesis rates of myofibrillar protein and phosphorylation of muscle anabolic signaling
|
5 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
October 1, 2014
Primary Completion (ACTUAL)
November 1, 2014
Study Completion (ACTUAL)
August 26, 2019
Study Registration Dates
First Submitted
September 3, 2019
First Submitted That Met QC Criteria
October 7, 2019
First Posted (ACTUAL)
October 10, 2019
Study Record Updates
Last Update Posted (ACTUAL)
October 10, 2019
Last Update Submitted That Met QC Criteria
October 7, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14234
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Muscle Protein Synthesis
-
McMaster UniversityCompleted
-
Maastricht University Medical CenterWithdrawn
-
Maastricht University Medical CenterCompletedMuscle Protein SynthesisNetherlands
-
University of ExeterQuornCompletedMuscle Protein SynthesisUnited Kingdom
-
McMaster UniversityCompletedMuscle Protein SynthesisCanada
-
University of Illinois at Urbana-ChampaignRecruiting
-
Maastricht University Medical CenterDSM Food SpecialtiesRecruiting
-
University of ExeterP.volve LLCCompletedMuscle Protein SynthesisUnited Kingdom
-
Maastricht University Medical CenterCompletedMuscle Protein SynthesisNetherlands
-
PepsiCo Global R&DCompletedMuscle Protein SynthesisCanada
Clinical Trials on Milk Protein Concentrate
-
University of LimerickMarigot Ltd.; Enterprise IrelandCompletedBioavailability of Amino Acids Following Oral Ingestion of Plant-Based Proteins in Young, Healthy MenIreland
-
Norwegian School of Sport SciencesThe Research Council of Norway; Arkansas Children's Hospital Research Institute and other collaboratorsCompletedHealthy | Elderly | YoungNorway
-
University of TorontoDairy Management Inc.RecruitingDietary ProteinsCanada
-
University of the Incarnate WordEnrolling by invitation
-
Norwegian School of Sport SciencesArkansas Children's Hospital Research Institute; TineCompletedHealthy Participants
-
Metabolic Technologies Inc.CompletedHealthy Men and WomenUnited States
-
Wageningen University and ResearchCompleted
-
Washington University School of MedicineProject Peanut Butter, Sierra LeoneCompleted
-
Wageningen University and ResearchCompleted
-
Auburn UniversityCompletedSkeletal Muscle