Progress in opioid reward research: From a canonical two-neuron hypothesis to two neural circuits

Pharmacol Biochem Behav. 2021 Jan:200:173072. doi: 10.1016/j.pbb.2020.173072. Epub 2020 Nov 20.

Abstract

Opioid abuse and related overdose deaths continue to rise in the United States, contributing to the national opioid crisis in the USA. The neural mechanisms underlying opioid abuse and addiction are still not fully understood. This review discusses recent progress in basic research dissecting receptor mechanisms and circuitries underlying opioid reward and addiction. We first review the canonical GABA-dopamine neuron hypothesis that was upheld for half a century, followed by major findings challenging this hypothesis. We then focus on recent progress in research evaluating the role of the mesolimbic and nigrostriatal dopamine circuitries in opioid reward and relapse. Based on recent findings that activation of dopamine neurons in the ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) is equally rewarding and that GABA neurons in the rostromedial tegmental nucleus (RMTg) and the substantia nigra pars reticula (SNr) are rich in mu opioid receptors and directly synapse onto midbrain DA neurons, we proposed that the RTMg→VTA → ventrostriatal and SNr → SNc → dorsostriatal pathways may act as the two major neural substrates underlying opioid reward and abuse. Lastly, we discuss possible integrations of these two pathways during initial opioid use, development of opioid abuse and maintenance of compulsive opioid seeking.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • Behavior, Addictive / metabolism
  • Dopamine / metabolism*
  • Dopaminergic Neurons / drug effects
  • Dopaminergic Neurons / metabolism*
  • Humans
  • Mesencephalon / drug effects
  • Mesencephalon / metabolism*
  • Neural Pathways / metabolism
  • Opioid-Related Disorders / metabolism*
  • Pars Compacta / drug effects
  • Pars Compacta / metabolism
  • Pars Reticulata / drug effects
  • Pars Reticulata / metabolism
  • Receptors, Opioid, mu / metabolism
  • Reward
  • Synapses / drug effects
  • Synapses / metabolism
  • Ventral Tegmental Area / drug effects
  • Ventral Tegmental Area / metabolism
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Analgesics, Opioid
  • Receptors, Opioid, mu
  • gamma-Aminobutyric Acid
  • Dopamine