Beta-Alanine supplementation augments muscle Carnosine and attenuates fatigue in trained sprinters
Carnosine is present in high concentrations in mammalian skeletal muscle and is thought to contribute to homeostasis during contractions as a pH buffer and as Ca++ sensitizer. The ingestion of beta-alanine, the ratelimiting precursor amino acid of the dipeptide carnosine (946;-alanyl-L-histidine) has been shown to elevate muscle carnosine content in untrained subjects. The present study aimed to investigate if oral supplementation of betaalanine during 4 weeks could elevate the calf muscle carnosine content in 400m sprint-trained competitive athletes. Second, we investigated if supplementation had an effect on the performance during a 400m indoor race and on the isokinetic and isometric muscle performance and fatigue. Methods: Fifteen male track-and-field athletes with a personal record on 400m below 52s were recruited from Flemish athletics clubs. A placebo-controlled, double-blind study was performed. Subjects were supplemented orally for 4 weeks with 4,8g/day placebo (maltodextrine) or betaalanine (Carnosyn, NAI, San Marcos, USA). Muscle carnosine concentration was determined by the C2-H imidazole peak of the proton NMR spectrum in a single voxel in the soleus and gastrocnemius. The time to complete 400m running was evaluated in an indoor 300m flat athletics track. Subjects also performed an isokinetic test consisting of 5 bouts of 30 maximal voluntary knee extensions on a Biodex isokinetic dynamometer. Additionally, subjects were asked to contract isometrically with their knee extensors at a target torque of 45% of MVC for as long as possible to determine the isometric endurance time. Results: The muscle carnosine content of the soleus increased by 47% (p<0,001) in the beta-alanine group, whereas it remained stable in the placebo group. The increase of carnosine in the gastrocnemius is significantly more pronounced in the beta-alanine group (+37%) than in the placebo group (+16%). A significant pre/post positive effect was observed for the average peak torque in the placebo group for the first two bouts, but not for the subsequent three bouts. Whereas for the beta-alanine group there was a significant pre/post main effect, indicating that average torque was higher is all five bouts post- vs. presupplementation. The knee extensor isometric endurance and the 400m race time were not affected by treatment. Conclusion: It can be concluded from this study that 1) proton NMR spectroscopy can be used to non-invasively and accurately quantify human muscle carnosine content; 2) muscle carnosine content can be substantially elevated by oral beta-alanine supplementation in sprint-trained athletes; 3) muscle carnosine loading significantly attenuates fatigue in repeated bouts of exhaustive dynamic contractions; 4) beta-alanine supplementation does not result in better 400m run performance.
© Copyright 2007 12th Annual Congress of the European College of Sport Science, Jyväskylä, Finland - July 11-14th 2007. All rights reserved.
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| Notations: | biological and medical sciences strength and speed sports training science |
| Published in: | 12th Annual Congress of the European College of Sport Science, Jyväskylä, Finland - July 11-14th 2007 |
| Language: | English |
| Published: |
Jyväskylä
2007
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| Online Access: | https://www.bisp-surf.de/Record/PU201707005044 |
| Pages: | 207 |
| Document types: | congress proceedings |
| Level: | advanced |