In Vivo and in Vitro Anabolic Potential of Essential Amino Acids Following Resistance Exercise

Interventional Clinical Trial

— DiEx  

Official title:

In Vivo and in Vitro Anabolic Potential of Essential Amino Acids Following Resistance Exercise

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05754125
• Other study ID #: DiEx
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 21, 2023
• Est. completion date: January 30, 2024

Study information

• Verified date: November 2023
• Source: University of Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study seeks to investigate the anabolic potential of a dileucine-enriched essential amino acid (EAA) formulation compared with a branched chain amino acid (BCAA) alternative and a collagen beverage on muscle protein anabolism and catabolism following a bout of resistance exercise training. To do this, investigators will employ a novel 'breath test' method developed in our laboratory as well as blood and urine sampling. The results of this study will allow us to better understand the anabolic potential of dileucine which could have implications for people engaging in regular resistance training (such as athletes) as well as people that need to preserve muscle mass (older people who are susceptible to anabolic resistance and sarcopenia, or muscle wasting).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 12
• Est. completion date: January 30, 2024
• Est. primary completion date: July 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• Trained individuals currently performing structured exercise (e.g., running, weightlifting, team-sport activity) at least 2 days per week for the previous 3 months

Exclusion Criteria:

• Inability to perform physical activity as determined by the PAR-Q

• Inability to adhere to protocol guidelines (e.g., alcohol, habitual diet)

• Regular tobacco use

• Illicit drug use (e.g., growth hormone, testosterone, etc.)

• Diagnosed medical condition under the care of a physician (e.g. type 2 diabetes)

• Inability to abstain from supplements (e.g. protein, creatine, HMB, BCAA, phosphatidic acid, etc.) at least three weeks before the trial

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

• Participants that are amenorrheic (females only)

• On medications that may interfere with protein metabolism (e.g. anti-inflammatory drugs, hormone therapy)

• Regular tobacco use (e.g. daily use of oral or inhaled tobacco)

• Illicit drug use (e.g. growth hormone, testosterone, etc.)

• Inability to comply with the study protocol as judged by the investigators

Related Conditions & MeSH terms

• Interventional

Intervention

Dietary Supplement:
• Di-Leucine Supplement
Participants will consume a amino acid supplement containing Di-Leucine following resistance exercise and their whole body anabolism will be determined over the subsequent 6 hours
• BCAA Supplement
Participants will consume a amino acid supplement containing branched chain amino acids (BCAA) following resistance exercise and their whole body anabolism will be determined over the subsequent hours
• Collagen Supplement
Participants will consume a amino acid supplement containing Collagen protein following resistance exercise and their whole body anabolism will be determined over the subsequent hours

Locations

Country	Name	City	State
Canada	Goldring Centre for High Performance Sport at the University of Toronto	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Whole-Body Protein Synthesis	Investigators will measure the enrichment of [13CO2] in the breath by isotope ratio mass spectrometry (IRMS) in atom percent excess (APE). The measurement of carbon dioxide production (VCO2) and stable isotope tracer enrichment in the breath allows for the assessment of the rate at which amino acids are used for energy (i.e., oxidized), rather than for protein synthesis (i.e., retained in the body) by calculating the fraction of expired CO2 that contains 13C. Leucine retention (umol/kg) will then be calculated from the difference between the known amount of leucine provided (ingested) and leucine oxidation (as determined from 13CO2 breath enrichment).	6 hours
Secondary	Urinary Measures (Muscle Protein Breakdown)	Investigators will measure urinary 3-methylhistidine (3MH) as an indirect marker of muscle protein breakdown over the course of the trial (6 hours) through pooled urine collection vs baseline urine.	6 hours
Secondary	Murine Cell-Based Experiments (ex-vivo experiments) -hypertrophy	Investigators will use human serum obtained from fasted and fed timepoints (15, 30, 45 and 60 minutes following beverage consumption) to condition cell culture media (20% volume). To determine the effects of using fasted and/or fed 'human-conditioned' culture media on cell growth, myotube diameter (hypertrophy) will be measured via microscopy following short term (4 hours) and long-term (24 hour) incubation in the human conditioned culture media.	60 minutes
Secondary	Murine Cell-Based Experiments (ex-vivo experiments) - Protein Synthesis	Investigators will use human serum obtained from fasted and fed timepoints (15, 30, 45 and 60 minutes following beverage consumption) to condition cell culture media (20% volume). To determine the effects of using fasted and/or fed 'human-conditioned' culture media on cell protein synthesis, puromycin incorporation (measure of protein synthesis) will be measured via western blot.	60 minutes
Secondary	Murine Cell-Based Experiments (ex-vivo experiments) - mTORC1 Signalling	Investigators will use human serum obtained from fasted and fed timepoints (15, 30, 45 and 60 minutes following beverage consumption) to condition cell culture media (20% volume). To determine the effects of using fasted and/or fed 'human-conditioned' culture media on cell anabolic signalling mTORC1 signalling will be measured via western blot.	60 minutes