NMDA receptor blockade prevents the increase in protein kinase C substrate (protein F1) phosphorylation produced by long-term potentiation

Brain Res. 1988 Aug 16;458(1):142-6. doi: 10.1016/0006-8993(88)90506-9.


Recent evidence has implicated activation of the N-methyl-D-aspartate (NMDA) class of glutamate receptor in the initiation of hippocampal long-term potentiation (LTP), an electrophysiological model of information storage in the brain. A separate line of evidence has suggested that activation of protein kinase C (PKC) and the consequent phosphorylation of its substrates is necessary for the maintenance of the LTP response. To determine if PKC activation is a consequence of NMDA receptor activation during LTP, we applied the NMDA receptor antagonist drug, DL-aminophosphonovalerate (APV) both immediately prior to and following high frequency stimulation, resulting in successful and unsuccessful blockade of LTP initiation, respectively. We then measured the phosphorylation of a PKC substrate (protein F1) in hippocampal tissue dissected from these animals. Only successful blockade of LTP initiation by prior application of APV was seen to block the LTP-associated increase in protein F1 phosphorylation measured in vitro (P less than 0.001 by ANOVA). This suggests that NMDA receptor-mediated initiation triggers maintenance processes that are, at least in part, mediated by protein F1 phosphorylation. These data provide the first evidence linking two mechanisms associated with LTP, NMDA receptor activation and PKC substrate phosphorylation.

Publication types

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

MeSH terms

  • 2-Amino-5-phosphonovalerate
  • Animals
  • Anticonvulsants / pharmacology
  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / pharmacology
  • GAP-43 Protein
  • Hippocampus / drug effects
  • Hippocampus / physiology*
  • Kinetics
  • Membrane Proteins / metabolism*
  • N-Methylaspartate
  • Nerve Tissue Proteins / metabolism*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Protein Kinase C / metabolism*
  • Rats
  • Reference Values
  • Valine / analogs & derivatives
  • Valine / pharmacology


  • Anticonvulsants
  • GAP-43 Protein
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Phosphoproteins
  • Aspartic Acid
  • N-Methylaspartate
  • 2-Amino-5-phosphonovalerate
  • Protein Kinase C
  • Valine