Loading…

Carnosine loading and washout in human skeletal muscles

1 Department of Movement and Sports Sciences, Ghent University, Ghent, Belgium; and 2 Department of Radiology, Ghent Institute for Functional and Metabolic Imaging, Ghent University, Ghent, Belgium Submitted 10 October 2008 ; accepted in final form 7 January 2009 Carnosine (β-alanyl- L -histidine) i...

Full description

Saved in:
Bibliographic Details
Published in:Journal of applied physiology (1985) 2009-03, Vol.106 (3), p.837-842
Main Authors: Baguet, Audrey, Reyngoudt, Harmen, Pottier, Andries, Everaert, Inge, Callens, Stefanie, Achten, Eric, Derave, Wim
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:1 Department of Movement and Sports Sciences, Ghent University, Ghent, Belgium; and 2 Department of Radiology, Ghent Institute for Functional and Metabolic Imaging, Ghent University, Ghent, Belgium Submitted 10 October 2008 ; accepted in final form 7 January 2009 Carnosine (β-alanyl- L -histidine) is present in high concentrations in human skeletal muscles. The oral ingestion of β-alanine, the rate-limiting precursor in carnosine synthesis, has been shown to elevate the muscle carnosine content both in trained and untrained humans. Little human data exist about the dynamics of the muscle carnosine content, its metabolic regulation, and its dependence on muscle fiber type. The present study aimed to investigate in three skeletal muscle types the supplementation-induced amplitude of carnosine synthesis and its subsequent elimination on cessation of supplementation (washout). Fifteen untrained males participated in a placebo-controlled double-blind study. They were supplemented for 5–6 wk with either 4.8 g/day β-alanine or placebo. Muscle carnosine was quantified in soleus, tibialis anterior, and medial head of the gastrocnemius by proton magnetic resonance spectroscopy (MRS), before and after supplementation and 3 and 9 wk into washout. The β-alanine supplementation significantly increased the carnosine content in soleus by 39%, in tibialis by 27%, and in gastrocnemius by 23% and declined postsupplementation at a rate of 2–4%/wk. Average muscle carnosine remained increased compared with baseline at 3 wk of washout (only one-third of the supplementation-induced increase had disappeared) and returned to baseline values within 9 wk at group level. Following subdivision into high responders (+55%) and low responders (+15%), washout period was 15 and 6 wk, respectively. In the placebo group, carnosine remained relatively constant with variation coefficients of 9–15% over a 3-mo period. It can be concluded that carnosine is a stable compound in human skeletal muscle, confirming the absence of carnosinase in myocytes. The present study shows that washout periods for crossover designs in supplementation studies for muscle metabolites may sometimes require months rather than weeks. ergogenic supplements; magnetic resonance spectroscopy; washout; carnosinase; skeletal muscle metabolism Address for reprint requests and other correspondence: W. Derave, Dept. of Movement and Sports Sciences, Ghent Univ., Watersportlaan 2, B-9000 Ghent, Belgium (e-mail: Wim.derave{at}ugen
ISSN:8750-7587
1522-1601
DOI:10.1152/japplphysiol.91357.2008