Downregulation of mGluR2/3 receptors during morphine withdrawal in rats impairs mGluR2/3- and NMDA receptor-dependent long-term depression in the nucleus accumbens

Neurosci Lett. 2019 Jan 18:690:76-82. doi: 10.1016/j.neulet.2018.10.018. Epub 2018 Oct 11.

Abstract

Drugs of abuse modify synaptic long-term potentiation and long-term depression (LTD) in the nucleus accumbens, and the impairment of synaptic plasticity in this brain region may be a universal feature of drug addiction. It is unknown whether metabotropic glutamate receptors (mGluRs) play a role in synaptic plasticity induced by drugs such as morphine. The neurochemical, electrophysiological, and Western blotting experiments reported here reveal a novel form of LTD in synapses of the shell region of the nucleus accumbens induced in vivo by low-frequency stimulation of the medial prefrontal cortex. This plasticity required the activation of N-methyl-d-aspartate receptors and mGluR2/3 but not mGluR5. The expression of mGluR2/3 was downregulated during withdrawal from repeated morphine exposure (10 days after the last injection), resulting in impaired low-frequency stimulation-induced LTD. These results indicate that withdrawal-induced mGluR2/3 downregulation alters neural plasticity after morphine exposure, which may be a mechanism contributing to drug addiction.

Keywords: Long-term depression; Metabotropic glutamate receptor 2/3; Morphine withdrawal; Nucleus accumbens; Synaptic plasticity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology
  • Amino Acids / pharmacology
  • Animals
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Down-Regulation / drug effects*
  • Electric Stimulation
  • Long-Term Synaptic Depression / drug effects*
  • Long-Term Synaptic Depression / physiology
  • Male
  • Microinjections
  • Morphine / adverse effects*
  • Nucleus Accumbens / drug effects*
  • Nucleus Accumbens / physiopathology
  • Prefrontal Cortex / physiology
  • Rats
  • Receptor, Metabotropic Glutamate 5 / physiology
  • Receptors, Metabotropic Glutamate / agonists
  • Receptors, Metabotropic Glutamate / biosynthesis
  • Receptors, Metabotropic Glutamate / physiology*
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / physiology*
  • Substance Withdrawal Syndrome / metabolism*
  • Substance Withdrawal Syndrome / physiopathology

Substances

  • Amino Acids
  • Bridged Bicyclo Compounds, Heterocyclic
  • Grm5 protein, mouse
  • LY 379268
  • Receptor, Metabotropic Glutamate 5
  • Receptors, Metabotropic Glutamate
  • Receptors, N-Methyl-D-Aspartate
  • metabotropic glutamate receptor 2
  • metabotropic glutamate receptor 3
  • 2-Amino-5-phosphonovalerate
  • Morphine