The goal of this clinical trial is to test ketone bodies in healthy elderly and young individuals. The main question it aims to answer are: • Do ketone bodies improve skeletal muscle function? Participants will ingest a ketone monoester and skeletal muscle function will then be evaluated by: * Special magnetic imaging techniques * Intravenous infusion of tracer-marked nutrients * Performance tests on a ergometer bike and in a dynamometer Researchers will compare the outcomes between within the young and elderly groups and between the young and the elderly group to investigate if age has an effect on the outcomes.
BACKGROUND With ageing, skeletal muscles metabolism changes and muscle function declines. This may lead to muscle weakness and increased risk of developing metabolic diseases. Ketone bodies, namely 3-hydroxybutyrate (3-OHB), is an energy substrate that may change the metabolism and improve efficiency of skeletal muscles in a setting of ageing. OBJECTIVE The study aims to investigate the effects of beta-hydroxybutyrate ingested as a monoester on skeletal muscle function and metabolism during muscle work in young and elderly individuals. DESIGN Healthy young (20-25 years) and elderly (65-85 years) untrained males will be paired based on age corrected VO2-max. Participants will be evaluated in a double blinded cross-over design on two study days: One day with ketone ester ingestion (D-beta-hydroxybutyrate/D-1,3-butanediol; KetoneAid Pro KE4), one day with ingestion of a volume and calorie and taste matched placebo (lipid emulsion). Blood ketone levels will be kept elevated through a sipping protocol. During both conditions a low glucose dose will be continuously infused to block physiological ketogenesis. The order of the study days will be randomized and interspaced by at least 4 weeks. On experimental days, participants meet fasted to perform voluntary contractions with tibialis anterior muscles in a MR compatible dynamometer while oxidative capacity, ATP generation, intramuscular pH, fatiguability and work efficiency is evaluated through 31P-MR spectroscopy. After, participants will bike at a fixed intensity (\~45% of Wmax) while lipid fluxes and glucose oxidation rates are measured by palmitate- and glucose tracer infusions and carbamide-corrected indirect calorimetry over 60 min. This was initially intended for both young and elderly individuals, but only involves the young group, as the elderly group had difficulties completing 60 min cycling. Lastly on the study days, participants will perform a cycling test as a measure of performance starting at 70 % of Wmax for 5 min thereafter increasing by 10 % of Wmax every 1 min until exhaustion. Muscle biopsies are obtained before (both groups) and just following fixed intensity cycle work (only young group). Adipose tissue biopsies are collected at the beginning of the experimental day (both groups) before ketone/placebo ingestion and after the constant load cycle work (only young group). Blood samples are performed throughout the day to assess substrate levels, hormones and for proteomics analysis. Before each study day, participant's activity level is measured for 7 days by accelerometry (ActiGraph). Participants will log their diet 3 days prior to each experimental day. Participants are asked to ingest a similar diet 2 days before both experimental days and to withstand from strenuous exercise 2 days prior to both experimental days. Participants are asked not to make any significant changes to their lifestyle while taking part in the study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
25
Ketone monoester
Steno Diabetes Center Aarhus
Aarhus, Aarhus N, Denmark
Work efficiency
External work performed by the ankle during dorsiflexion per ATP consumed. ATP consumption is assessed by 31P-MRS while external force is measured by the dynamometer.
Time frame: Over 60 minutes on each of the two experimental days.
Oxidative capacity
Assessed by 31P-MRS as phosphocreatine resynthesis.
Time frame: Over 20 minutes at each of the two experimental days.
Glucose oxidation rates (only young group)
Assessed by measuring tracer dilution from blood samples obtained during 3H-glucose infusion while cycling at a fixed intensity.
Time frame: At 10 minute intervals over the last 30 min of the 90 min fixed intensity cycling on each experimental day.
Palmitate flux (only young group)
Assessed by measuring tracer dilution from blood samples obtained during 3H-palmitate infusion while cycling at a fixed intensity.
Time frame: At 10 minute intervals over the last 30 min of the 90 min fixed intensity cycling on each experimental day.
ATP generation
ATP generated from different pathways (glycolytic, oxidative, phosphocreatine) assessed by 31P-MRS.
Time frame: Over 30 minutes at each of the two experimental days.
Mitochondrial function
Assessed by high-resolution respirometry on muscle biopsies
Time frame: Just before and immediately after the constant load cycling at each of the two experimental days.
Intramuscular pH
Measurements at rest rest and during work assessed by 31P-MRS
Time frame: Over 60 minutes at each of the two experimental days.
Blood 3-OHB
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Blood glucose
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Blood free fatty acids
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Cycle performance
Assessed by a performance test on a bike ergometer with incremental load. The test continues until failure. The test outcome is the power generated at time of failure.
Time frame: 5-8 minutes during each of the two experimental days
Rating of perceived exertion (only young group)
Subjective measure of exertion during cycling evaluated by reporting on a number assessment scale (Borg scale (6-20)).
Time frame: After 30, 60 and 90 minutes of fixed intensity cycling and just after the incremental performance test.
Tibialis anterior fatigue
Tibialis anterior fatigue assessed by the dynamometer during 3 minutes of dorsiflexion at a fixed resistance.
Time frame: Over 3 minutes on each of the two experimental days.
Blood growth hormone
Blood concentration measured by blood sampling
Time frame: During experimental days
Blood insulin
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
AMPK phosphorylation (only young group)
From muscle biopsies
Time frame: Just before and immediately after the constant load cycling at each of the two experimental days.
Blood glucagon
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Blood pH
Assessed from arterial blood samples
Time frame: During each of the two experimental days
Blood catecholamines
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Blood cortisol
Blood concentration measured by blood sampling
Time frame: During each of the two experimental days
Intramuscular lipid content
Concentration measured in muscle biopsies
Time frame: At the beginning and at the end of each of the two experimental days
Intramuscular glycogen content
Concentration measured in muscle biopsies
Time frame: Just before and immediately after the constant load cycling at each of the two experimental days.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.