2-Deoxyglucose and NMDA inhibit protein synthesis in neurons and regulate phosphorylation of elongation factor-2 by distinct mechanisms

J Neurochem. 2006 Feb;96(3):815-24. doi: 10.1111/j.1471-4159.2005.03601.x. Epub 2006 Jan 9.

Abstract

Cerebral ischaemia is associated with brain damage and inhibition of neuronal protein synthesis. A deficit in neuronal metabolism and altered excitatory amino acid release may both contribute to those phenomena. In the present study, we demonstrate that both NMDA and metabolic impairment by 2-deoxyglucose or inhibitors of mitochondrial respiration inhibit protein synthesis in cortical neurons through the phosphorylation of eukaryotic elongation factor (eEF-2), without any change in phosphorylation of initiation factor eIF-2alpha. eEF-2 kinase may be activated both by Ca(2+)-independent AMP kinase or by an increase in cytosolic Ca2+. Although NMDA decreases ATP levels in neurons, only the effects of 2-deoxyglucose on protein synthesis and phosphorylation of elongation factor eEF-2 were reversed by Na(+) pyruvate. Protein synthesis inhibition by 2-deoxyglucose was not as a result of a secondary release of glutamate from cortical neurons as it was not prevented by the NMDA receptor antagonist 5-methyl-10,11-dihydro-5H-dibenzo-(a,d)-cyclohepten-5,10-imine hydrogen maleate (MK 801), nor to an increase in cytosolic-free Ca2+. Conversely, 2-deoxyglucose likely activates eEF-2 kinase through a process involving phosphorylation by AMP kinase. In conclusion, we provide evidence that protein synthesis can be inhibited by NMDA and metabolic deprivation by two distinct mechanisms involving, respectively, Ca(2+)-dependent and Ca(2+)-independent eEF-2 phosphorylation.

Publication types

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

MeSH terms

  • Animals
  • Antimetabolites / pharmacology*
  • Blotting, Western / methods
  • Calcium / metabolism
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Deoxyglucose / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Embryo, Mammalian
  • Enzyme Inhibitors / pharmacology
  • Excitatory Amino Acid Agonists / pharmacology*
  • Ionophores / pharmacology
  • Leucine / metabolism
  • Mice
  • Models, Biological
  • N-Methylaspartate / pharmacology*
  • Neurons / drug effects*
  • Neurons / physiology
  • Oligomycins / pharmacology
  • Peptide Elongation Factor 2 / metabolism*
  • Phosphorylation / drug effects
  • Protein Kinases / metabolism
  • Protein Synthesis Inhibitors / pharmacology
  • Pyruvic Acid / pharmacokinetics
  • Sodium Azide / pharmacology
  • TOR Serine-Threonine Kinases
  • Time Factors
  • Tritium / metabolism

Substances

  • Antimetabolites
  • Enzyme Inhibitors
  • Excitatory Amino Acid Agonists
  • Ionophores
  • Oligomycins
  • Peptide Elongation Factor 2
  • Protein Synthesis Inhibitors
  • Tritium
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone
  • N-Methylaspartate
  • Pyruvic Acid
  • Sodium Azide
  • Deoxyglucose
  • Protein Kinases
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Leucine
  • Calcium