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Ensayo controlado aleatorizado2005Financiación no declaradaSolo mecanismos

Increased IGF mRNA in human skeletal muscle after creatine supplementation

Deldicque L, Louis M, Theisen D, Nielens H, Dehoux M, Thissen JP, Rennie MJ, Francaux M

Medicine and science in sports and exercise · 86 citas

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Financiación no declaradaSolo mecanismos

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Solo mecanismos

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2005-05-01 · Med Sci Sports Exerc · vol. 37 · número 5 · págs. 731–736
Editorial
Lippincott Williams & Wilkins
Citado
140 citas · más que el 92% de estudios similares · 3.5× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
30 trabajos
Acceso
Acceso abierto (copia en repositorio) · OTHER-OA
Áreas de investigación
Muscle metabolism and nutrition · Muscle Physiology and Disorders · Growth Hormone and Insulin-like Growth Factors
Palabras clave
creatine supplementation, insulin-like growth factor I, insulin-like growth factor II, skeletal muscle, resistance training, muscle anabolism, p70S6K, 4E-BP1, mTOR signaling, mRNA expression, vastus lateralis, lean body mass
MeSH
muscle, skeletal, humans, creatine, ribosomal protein s6 kinases, 70-kda, insulin-like growth factor i, insulin-like growth factor ii, adaptor proteins, signal transducing, carrier proteins, cell cycle proteins, phosphoproteins, rna, messenger, biopsy, exercise, cross-over studies, double-blind method, phosphorylation, time factors, adult, male

8 autores

  • Louise Deldicque🇧🇪UCLouvain; KU Leuven
  • Magali Louis🇧🇪UCLouvain; KU Leuven
  • Daniel Theisen🇧🇪UCLouvain; KU Leuven
  • Henri Nielens🇧🇪UCLouvain; KU Leuven
  • MISCHA L DEHOUX🇧🇪UCLouvain; KU Leuven
  • Jean‐Paul Thissen🇧🇪UCLouvain; KU Leuven
  • Michael J. Rennie🇬🇧University of Nottingham
  • Marc Francaux🇧🇪UCLouvain; KU Leuven

Resumen

El texto original del estudio, en el idioma en que se publicó.

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 p70(s6k) 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 x d(-1)). For the first 3 h postexercise, the subjects were fed with a drink containing maltodextrin (0.3 g x kg(-1) body weight x h(-1)) and protein (0.08 g x kg(-1) body weight x 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 p70(s6k) 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.

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