Treatment for psychological dependence on morphine: usefulness of inhibiting NMDA receptor and its associated protein kinase in the nucleus accumbens

Life Sci. 2005 Sep 16;77(18):2207-20. doi: 10.1016/j.lfs.2005.04.015.

Abstract

A growing body of evidence indicates that the mesolimbic dopaminergic (DAergic) pathway projecting from the ventral tegmental area (VTA) to the nucleus accumbens (N.Acc.) play a critical role in the initiation of psychological dependence on morphine. As well as DAergic system, the involvement of non-DAergic neurotransmitter and neuromodulator systems in rewarding effects induced by morphine has been recently documented. We previously demonstrated that the morphine-induced rewarding effect was dramatically suppressed by co-treatment with NMDA receptor antagonists, such as dizocilpine (MK-801), ketamine and ifenprodil. Therefore, we propose here that inhibiting the N-methyl-D-aspartate (NMDA) receptor and its associated protein kinase in the N.Acc. is useful for the treatment for psychological dependence on morphine. The following review provides a summary of recent our findings regarding the role of NMDA receptor and its associated protein kinase in the development of psychological dependence on morphine.

Publication types

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

MeSH terms

  • Animals
  • Disks Large Homolog 4 Protein
  • Dizocilpine Maleate
  • Excitatory Amino Acid Antagonists / pharmacology
  • Excitatory Amino Acid Antagonists / therapeutic use*
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Ketamine
  • Membrane Proteins / metabolism
  • Mice
  • Morphine Dependence / drug therapy*
  • Morphine Dependence / metabolism
  • Morphine Dependence / psychology*
  • Nucleus Accumbens / metabolism*
  • Piperidines
  • Protein Kinase C / metabolism
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Signal Transduction / drug effects*

Substances

  • DLG4 protein, human
  • Disks Large Homolog 4 Protein
  • Excitatory Amino Acid Antagonists
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Piperidines
  • Receptors, N-Methyl-D-Aspartate
  • Ketamine
  • Dizocilpine Maleate
  • Protein Kinase C
  • ifenprodil