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In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle.

Publication ,  Journal Article
Viguerie, N; Clement, K; Barbe, P; Courtine, M; Benis, A; Larrouy, D; Hanczar, B; Pelloux, V; Poitou, C; Khalfallah, Y; Barsh, GS; Thalamas, C ...
Published in: The Journal of clinical endocrinology and metabolism
May 2004

The stress hormone epinephrine produces major physiological effects on skeletal muscle. Here we determined skeletal muscle mRNA expression profiles before and during a 6-h epinephrine infusion performed in nine young men. Stringent statistical analysis of data obtained using 43000 cDNA element microarrays showed that 1206 and 474 genes were up- and down-regulated, respectively. Microarray data were validated using reverse transcription quantitative PCR. Gene classification was performed through data mining of Gene Ontology annotations, cluster analysis of regulated genes among 14 human tissues, and correlation analysis of mRNA and clinical parameter variations. Evidence of an autoregulatory control was provided by the regulation of key genes of the cAMP-dependent transcription pathway. Genes with known functional cAMP response elements were regulated by the hormone. The impact on metabolism was illustrated by coordinated regulations of genes involved in carbohydrate and protein metabolisms. Epinephrine had a profound effect on genes involved in immunity and inflammatory response, a previously unappreciated aspect of catecholamine action. Information on 526 mRNAs corresponded to genes of unknown function. These data define the molecular signatures of epinephrine action in human skeletal muscle. They may contribute to the understanding of skeletal muscle alterations observed in pathological conditions characterized by sympathetic nervous system overdrive.

Duke Scholars

Published In

The Journal of clinical endocrinology and metabolism

DOI

EISSN

1945-7197

ISSN

0021-972X

Publication Date

May 2004

Volume

89

Issue

5

Start / End Page

2000 / 2014

Related Subject Headings

  • Up-Regulation
  • Stress, Physiological
  • Signal Transduction
  • RNA, Messenger
  • Proteins
  • Oligonucleotide Array Sequence Analysis
  • Muscle, Skeletal
  • Metabolism
  • Male
  • Humans
 

Citation

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ICMJE
MLA
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Viguerie, N., Clement, K., Barbe, P., Courtine, M., Benis, A., Larrouy, D., … Langin, D. (2004). In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle. The Journal of Clinical Endocrinology and Metabolism, 89(5), 2000–2014. https://doi.org/10.1210/jc.2003-031733
Viguerie, Nathalie, Karine Clement, Pierre Barbe, Melanie Courtine, Arriel Benis, Dominique Larrouy, Blaise Hanczar, et al. “In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle.The Journal of Clinical Endocrinology and Metabolism 89, no. 5 (May 2004): 2000–2014. https://doi.org/10.1210/jc.2003-031733.
Viguerie N, Clement K, Barbe P, Courtine M, Benis A, Larrouy D, et al. In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle. The Journal of clinical endocrinology and metabolism. 2004 May;89(5):2000–14.
Viguerie, Nathalie, et al. “In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle.The Journal of Clinical Endocrinology and Metabolism, vol. 89, no. 5, May 2004, pp. 2000–14. Epmc, doi:10.1210/jc.2003-031733.
Viguerie N, Clement K, Barbe P, Courtine M, Benis A, Larrouy D, Hanczar B, Pelloux V, Poitou C, Khalfallah Y, Barsh GS, Thalamas C, Zucker J-D, Langin D. In vivo epinephrine-mediated regulation of gene expression in human skeletal muscle. The Journal of clinical endocrinology and metabolism. 2004 May;89(5):2000–2014.
Journal cover image

Published In

The Journal of clinical endocrinology and metabolism

DOI

EISSN

1945-7197

ISSN

0021-972X

Publication Date

May 2004

Volume

89

Issue

5

Start / End Page

2000 / 2014

Related Subject Headings

  • Up-Regulation
  • Stress, Physiological
  • Signal Transduction
  • RNA, Messenger
  • Proteins
  • Oligonucleotide Array Sequence Analysis
  • Muscle, Skeletal
  • Metabolism
  • Male
  • Humans