Activation by insulin and amino acids of signaling components leading to translation initiation in skeletal muscle of neonatal pigs is developmentally regulated

Am J Physiol Endocrinol Metab. 2007 Dec;293(6):E1597-605. doi: 10.1152/ajpendo.00307.2007. Epub 2007 Sep 18.

Abstract

Insulin and amino acids act independently to stimulate protein synthesis in skeletal muscle of neonatal pigs, and the responses decrease with development. The purpose of this study was to compare the separate effects of fed levels of INS and AA on the activation of signaling components leading to translation initiation and how these responses change with development. Overnight-fasted 6- (n = 4/group) and 26-day-old (n = 6/ group) pigs were studied during 1) euinsulinemic-euglycemiceuaminoacidemic conditions (controls), 2) euinsulinemic-euglycemichyperaminoacidemic clamps (AA), and 3) hyperinsulinemic-euglycemic-euaminoacidemic clamps (INS). INS, but not AA, increased the phosphorylation of protein kinase B (PKB) and tuberous sclerosis 2 (TSC2). Both INS and AA increased protein synthesis and the phosphorylation of mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase-1, and eukaryotic initiation factor (eIF)4E-binding protein 1 (4E-BP1), and these responses were higher in 6-day-old compared with 26-day-old pigs. Both INS and AA decreased the binding of 4E-BP1 to eIF4E and increased eIF4E binding to eIF4G; these effects were greater in 6-day-old than in 26-day-old pigs. Neither INS nor AA altered the composition of mTORC1 (raptor, mTOR, and GbetaL) or mTORC2 (rictor, mTOR, and GbetaL) complexes. Furthermore, neither INS, AA, nor age had any effect on the abundance of Rheb and the phosphorylation of AMP-activated protein kinase and eukaryotic elongation factor 2. Our results suggest that the activation by insulin and amino acids of signaling components leading to translation initiation is developmentally regulated and parallels the developmental decline in protein synthesis in skeletal muscle of neonatal pigs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • AMP-Activated Protein Kinases
  • Age Factors
  • Amino Acids / administration & dosage
  • Amino Acids / blood
  • Amino Acids / pharmacology*
  • Amino Acids, Branched-Chain / blood
  • Amino Acids, Branched-Chain / pharmacology
  • Animals
  • Animals, Newborn
  • Blood Glucose / metabolism
  • Eukaryotic Initiation Factor-4E / metabolism
  • Eukaryotic Initiation Factor-4G / metabolism
  • Gene Expression Regulation, Developmental / drug effects
  • Insulin / administration & dosage
  • Insulin / blood
  • Insulin / pharmacology*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Multienzyme Complexes / metabolism
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism
  • Peptide Elongation Factor 2 / metabolism
  • Phosphorylation / drug effects
  • Protein Binding / drug effects
  • Protein Biosynthesis / drug effects*
  • Protein Kinases / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Sus scrofa
  • TOR Serine-Threonine Kinases
  • Transcription Factors / metabolism
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins / metabolism

Substances

  • Amino Acids
  • Amino Acids, Branched-Chain
  • Blood Glucose
  • Eukaryotic Initiation Factor-4E
  • Eukaryotic Initiation Factor-4G
  • Insulin
  • Intracellular Signaling Peptides and Proteins
  • Multienzyme Complexes
  • Peptide Elongation Factor 2
  • Transcription Factors
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins
  • Protein Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Ribosomal Protein S6 Kinases, 70-kDa
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases