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Increased IGF mRNA in Human Skeletal Muscle after Creatine Supplementation

DELDICQUE, LOUISE1; LOUIS, MAGALI1; THEISEN, DANIEL1; NIELENS, HENRI1; DEHOUX, MISCHAËL2; THISSEN, JEAN-PAUL2; RENNIE, MICHAEL J.3; FRANCAUX, MARC1

Medicine & Science in Sports & Exercise: May 2005 - Volume 37 - Issue 5 - pp 731-736
Basic Sciences: Original Investigations

Purpose: We hypothesized that creatine supplementation would facilitate muscle anabolism by increasing the expression of growth factors and the phosphorylation of anabolic signaling molecules; we therefore tested the responses of mRNA for IGF-I and IGF-II and the phosphorylation state of components of anabolic signaling pathways p70s6k and 4E-BP1 to a bout of high-intensity resistance exercise after 5 d of creatine supplementation.

Methods: In a double-blind cross-over design, muscle biopsies were taken from the m. vastus lateralis at rest and 3 and 24 h postexercise in subjects who had taken creatine or placebo for 5 d (21 g·d−1). For the first 3 h postexercise, the subjects were fed with a drink containing maltodextrin (0.3 g·kg−1 body weight·h−1) and protein (0.08 g·kg−1 body weight·h−1).

Results: After creatine supplementation, resting muscle expressed more mRNA for IGF-I (+30%, P < 0.05) and IGF-II (+40%, P = 0.054). Exercise caused an increase by 3 h postexercise in IGF-I (+24%, P < 0.05) and IGF-II (+48%, P < 0.05) and by 24 h postexercise in IGF-I (+29%, P < 0.05), but this effect was not potentiated by creatine supplementation. The phosphorylation states of p70s6k and 4E-BP1 were not affected by creatine at rest; phosphorylation of both increased (150–400%, P < 0.05) to similar levels under placebo and creatine conditions at 3 h postexercise plus feeding. However, the phosphorylation state of 4E-BP1 was higher in the creatine versus placebo condition at 24 h postexercise.

Conclusion: The increase in lean body mass often reported after creatine supplementation could be mediated by signaling pathway(s) involving IGF and 4E-BP1.

1Department of Physical Education and Rehabilitation, Faculty of Medicine, Catholic University of Louvain, Louvain-la-Neuve, BELGIUM; 2Unit of Diabetology and Nutrition, Faculty of Medicine, Catholic University of Louvain, Brussels, BELGIUM; and 3School of Biomedical Sciences, University of Nottingham Graduate Entry Medical School, Derby, UNITED KINGDOM

Address for correspondence: Prof. Marc Francaux, Department of Physical Education and Rehabilitation, Place Pierre de Coubertin-1, B-1348 Louvain-la-Neuve, Belgium; E-mail: marc.francaux@edph.ucl.ac.be.

Submitted for publication October 2004.

Accepted for publication December 2004.

This work is granted by the “Fonds de la Recherche Scientifique Médicale” (3.4574.03), Belgium.

©2005The American College of Sports Medicine