Synaptic Plasticity in the Nucleus Accumbens: Lessons Learned from Experience

ACS Chem Neurosci. 2018 Sep 19;9(9):2114-2126. doi: 10.1021/acschemneuro.7b00420. Epub 2018 Jan 24.

Abstract

Synaptic plasticity contributes to behavioral adaptations. As a key node in the reward pathway, the nucleus accumbens (NAc) is important for determining motivation-to-action outcomes. Across animal models of motivation including addiction, depression, anxiety, and hedonic feeding, selective recruitment of neuromodulatory signals and plasticity mechanisms have been a focus of physiologists and behaviorists alike. Experience-dependent plasticity mechanisms within the NAc vary depending on the distinct afferents and cell-types over time. A greater understanding of molecular mechanisms determining how these changes in synaptic strength track with behavioral adaptations will provide insight into the process of learning and memory along with identifying maladaptations underlying pathological behavior. Here, we summarize recent findings detailing how changes in NAc synaptic strength and mechanisms of plasticity manifest in various models of motivational disorders.

Keywords: Nucleus accumbens; glia; glutamate; opioids; plasticity; serotonin.

Publication types

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

MeSH terms

  • Animals
  • Anxiety / metabolism
  • Anxiety / physiopathology
  • Behavior, Addictive / metabolism
  • Behavior, Addictive / physiopathology
  • Depression / metabolism
  • Depression / physiopathology
  • Endocannabinoids / metabolism
  • Feeding Behavior / physiology
  • Glutamic Acid / metabolism
  • Humans
  • Learning
  • Motivation*
  • Neuroglia
  • Neuronal Plasticity / physiology*
  • Nucleus Accumbens / metabolism
  • Nucleus Accumbens / physiology*
  • Nucleus Accumbens / physiopathology
  • Opioid Peptides / metabolism
  • Receptors, AMPA / metabolism
  • Receptors, Cannabinoid / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Receptors, Opioid / metabolism
  • Reward
  • Serotonin / metabolism

Substances

  • Endocannabinoids
  • Opioid Peptides
  • Receptors, AMPA
  • Receptors, Cannabinoid
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Opioid
  • Serotonin
  • Glutamic Acid