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Clinical Trials/NCT06567665
NCT06567665
Recruiting
Not Applicable

Leucine Supplementation Strategies to Enhance Muscle Anabolic Responses in Older Age

University of Nottingham1 site in 1 country10 target enrollmentAugust 5, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Muscle Protein Synthesis
Sponsor
University of Nottingham
Enrollment
10
Locations
1
Primary Endpoint
Muscle protein synthesis in response to leucine feeding
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Sarcopenia describes the progressive decline of muscle mass and strength with advancing age and is associated with increased frailty and morbidity, however we do not currently have an effective treatment. Protein feeding and exercise is known to increase muscle mass, but aged muscle shows a lower response to these stimuli leading to muscle loss over time. We do know that ingesting leucine, a building block of protein, can overcome this reduced response to protein feeding and exercise leading to increased muscle mass in older people. However, we do not understand when the optimum time to ingest leucine is to maximise muscle mass after exercise in older people. In this study we will examine the effect of feeding leucine after exercise either with a meal or between meals.

Registry
clinicaltrials.gov
Start Date
August 5, 2024
End Date
August 5, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male, 65-75 years of age
  • BMI 18-28 kg/m2
  • Non smoker
  • Not performing regular resistance type exercise
  • Participant is willing and able to give informed consent for participation in the study

Exclusion Criteria

  • A BMI \<18 or \>28 kg·m-2
  • Active cardiovascular disease: uncontrolled hypertension (BP \> 160/100), angina, heart failure (class III/IV), arrhythmia, right to left cardiac shunt or recent cardiac event
  • Cerebrovascular disease: previous stroke, aneurysm (large vessel or intracranial)
  • Respiratory disease including pulmonary hypertension or chronic obstructive pulmonary disease (COPD)
  • Metabolic disease: hyper and hypo parathyroidism, untreated hyper and hypothyroidism, Cushing's disease, types 1 or 2 diabetes (treated and untreated), inborn/ congenital errors of metabolism (e.g. phenylketonuria (PKU), galactosaemia)
  • Active inflammatory bowel disease
  • Acute infection
  • Acute or chronic renal disease
  • Malignancy (or history of malignancy with 5 y)
  • Recent steroid treatment (within 6 mo), or hormone replacement therapy

Outcomes

Primary Outcomes

Muscle protein synthesis in response to leucine feeding

Time Frame: 7 days

To quantify muscle protein synthesis in response to feeding leucine with a meal or in-between meals using mass spectrometry.

Secondary Outcomes

  • Measure muscle anabolic and catabolic signalling pathways in response to leucine feeding(7 days)

Study Sites (1)

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