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J Appl Physiol 104: 371-378, 2008. First published November 29, 2007; doi:10.1152/japplphysiol.00873.2007
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Effects of resistance exercise with and without creatine supplementation on gene expression and cell signaling in human skeletal muscle

Louise Deldicque,1 Philip Atherton,2 Rekha Patel,2 Daniel Theisen,1 Henri Nielens,1 Michael J. Rennie,2 and Marc Francaux1

1Department of Physical Education and Rehabilitation, Université catholique de Louvain, Louvain-la-Neuve, Belgium; and 2University of Nottingham, School of Graduate Entry Medicine and Health, City Hospital, Derby, United Kingdom

Submitted 14 August 2007 ; accepted in final form 23 November 2007

To test the hypothesis that creatine supplementation would enhance the anabolic responses of muscle cell signaling and gene expression to exercise, we studied nine subjects who received either creatine or a placebo (maltodextrin) for 5 days in a double-blind fashion before undergoing muscle biopsies: at rest, immediately after exercise (10 x 10 repetitions of one-leg extension at 80% 1 repetition maximum), and 24 and 72 h later (all in the morning after fasting overnight). Creatine supplementation decreased the phosphorylation state of protein kinase B (PKB) on Thr308 at rest by 60% (P < 0.05) and that of eukaryotic initiation factor 4E-binding protein on Thr37/46 (4E-BP1) by 30% 24 h postexercise (P < 0.05). Creatine increased mRNA for collagen 1 ({alpha}1), glucose transporter-4 (GLUT-4), and myosin heavy chain I at rest by 250%, 45%, and 80%, respectively, and myosin heavy chain IIA (MHCIIA) mRNA immediately after exercise by 70% (all P < 0.05). Immediately after exercise, and independent of creatine, mRNA for muscle atrophy F-box (MAFbx), MHCIIA, peroxisome proliferator-activated receptor {gamma} coactivator-1{alpha}, and interleukin-6 were upregulated (60–350%; P < 0.05); the phosphorylation state of p38 both in the sarcoplasm and nucleus were increased (12- and 25-fold, respectively; both P < 0.05). Concurrently, the phosphorylation states of PKB (Thr308) and 4E-BP1 (Thr37/46) were decreased by 50% and 75%, respectively (P < 0.05). Twenty-four hours postexercise, MAFbx, myostatin, and GLUT-4 mRNA expression decreased below preexercise values (–35 to –50%; P < 0.05); calpain 1 mRNA increased 70% 72 h postexercise (P < 0.05) and at no other time. In conclusion, 5 days of creatine supplementation do not enhance anabolic signaling but increase the expression of certain targeted genes.

mitogen-activated protein kinase; protein kinase B; protein synthesis



Address for reprint requests and other correspondence: M. Francaux, Place Pierre de Coubertin 1, B-1348 Louvain-la-Neuve, Belgium (e-mail: marc.francaux{at}uclouvain.be)




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M. J. Drummond, H. C. Dreyer, C. S. Fry, E. L. Glynn, and B. B. Rasmussen
Nutritional and contractile regulation of human skeletal muscle protein synthesis and mTORC1 signaling
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[Abstract] [Full Text] [PDF]




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