The present study will seek to quantify whether a period of HIIT alongside β-alanine supplementation will improve the adaptation to training, and therefore performance, more than a period of HIIT alone.
Whilst high-intensity interval training (HIIT) is a powerful stimulus to increase endurance exercise performance, there are potential nutritional interventions that can be put in place to further increase performance gains. Energy for the contraction of muscles is created in the mitochondria. HIIT can improve the function of mitochondria, therefore improving performance. Β-alanine is a commonly used supplement that can improve exercise performance by increasing the amount of carnosine in muscle. Carnosine has many functions that may help improve exercise capacity. The present study will seek to quantify whether a period of HIIT alongside β-alanine supplementation will improve the adaptation to training, and therefore performance, more than a period of HIIT alone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
26
N/A: see arm description
N/A: see arm description
School of Sport and Health Sciences
Exeter, Devon, United Kingdom
Change from baseline work done on a cycle ergometer in a cycling capacity test at 110%VO2max following a period of 4 weeks of beta-alanine supplementation and then 8 weeks of beta-alanine supplementation and high intensity interval training
Subjects will have previously performed an incremental test to exhaustion (VO2max test). A work-load that corresponds to 110 % of the peak power output (Wmax) will be calculated, and participants will be asked to cycle at this power output until volitional exhaustion. This test will be preceded but a bout of 90-minute cycling at 65%VO2max. Tests will be performed on a Lode Excalibur Sport, and software linked to the bike will record data.
Time frame: At weeks 0, 4 and 12 of study.
VO2max
VO2max will be determined from data collected through a metabolic cart. It will be measured during an incremental test to exhaustion performed on a cycle ergometer.
Time frame: At weeks 0, 4, 8 and 12 of study.
Substrate utilisation
Substrate utilisation will be calculated from data collected through a metabolic cart and its software. It will be measured during the 90-minute steady-state cycle for 4 periods of 3 minutes. Carbohydrate and lipid oxidation rates will be calculated using equations by Jeukendrup \& Wallis (2005).
Time frame: At weeks 0, 4 and 12 of study.
Muscle carnosine concentration
Using the Bergstrom muscle biopsy technique. Samples will be frozen immediately in liquid nitrogen and will be later analysed using validated techniques
Time frame: At weeks 0, 4 and 12 of study.
Muscle enzyme (citrate synthase, hexokinase, β-HAD, PFK) activity
Using the Bergstrom muscle biopsy technique. Samples will be frozen immediately in liquid nitrogen and will be later analysed using validated techniques
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Time frame: At weeks 0, 4 and 12 of study.
Muscle buffering capacity
Using the Bergstrom muscle biopsy technique. Samples will be frozen immediately in liquid nitrogen and will be later analysed using validated techniques
Time frame: At weeks 0, 4 and 12 of study.
Muscle metabolites (AMP, ADP, ATP, Pi, IMP, PCr, Cr, lactate, pyruvate, NAD+/NADH, glucose, G6P, citrate)
Using the Bergstrom muscle biopsy technique. Samples will be frozen immediately in liquid nitrogen and will be later analysed using validated techniques
Time frame: At weeks 0, 4 and 12 of study.
Muscle gene expression
Using the Bergstrom muscle biopsy technique. Samples will be frozen immediately in liquid nitrogen and will be later analysed using validated techniques
Time frame: At weeks 0, 4 and 12 of study.
Plasma metabolites (NEFA, glucose, glycerol, lactate)
A cannula will be used to draw blood from subjects at several time points. Whole blood will be centrifuged immediately and its plasma split into aliquots and stored in a -80°C freezer for later analysis.
Time frame: At weeks 0, 4 and 12 of study.
Heart rate
Heart rate will be measured throughout with the use of a heart rate monitor.
Time frame: At weeks 0, 4 and 12 of study, and through whole training period (weeks 8-12)