Post-transcriptional gene silencing of ribosomal protein S6 kinase 1 restores insulin action in leucine-treated skeletal muscle

Atul Deshmukh, F Salehzadeh, S Metayer-Coustard, R Fahlman, K S Nair, L Al-Khalili

10 Citations (Scopus)

Abstract

Excessive nutrients, especially amino acids, impair insulin action on glucose metabolism in skeletal muscle. We tested the hypothesis that the branched-chain amino acid leucine reduces acute insulin action in primary myotubes via a negative feedback mechanism involving ribosomal protein S6 kinase 1 (S6K1). The effect of S6K1 on glucose metabolism was determined by applying RNA interference (siRNA). Leucine (5 mM) reduced glucose uptake and incorporation to glycogen by 13% and 22%, respectively, compared to the scramble siRNA-transfected control at the basal level. Leucine also reduced insulin-stimulated Akt phosphorylation, glucose uptake and glucose incorporation to glycogen (39%, 39% and 37%, respectively), and this reduction was restored after S6K1 silencing. Depletion of S6K1 enhanced basal glucose utilization and protected against the development of impaired insulin action, in response to excessive leucine. In conclusion, S6K1 plays an important role in the regulation of insulin action on glucose metabolism in skeletal muscle.

Original languageEnglish
JournalCellular and molecular life sciences : CMLS
Volume66
Issue number8
Pages (from-to)1457-66
Number of pages10
ISSN1420-682X
DOIs
Publication statusPublished - Apr 2009
Externally publishedYes

Keywords

  • Female
  • Glucose
  • Glycogen
  • Humans
  • Insulin
  • Leucine
  • Male
  • Middle Aged
  • Muscle, Skeletal
  • RNA Interference
  • RNA, Small Interfering
  • Ribosomal Protein S6 Kinases, 70-kDa
  • Ribosomal Proteins
  • Journal Article
  • Research Support, Non-U.S. Gov't

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