Sustained rescue of prefrontal circuit dysfunction by antidepressant-induced spine formation

Science. 2019 Apr 12;364(6436):eaat8078. doi: 10.1126/science.aat8078.

Abstract

The neurobiological mechanisms underlying the induction and remission of depressive episodes over time are not well understood. Through repeated longitudinal imaging of medial prefrontal microcircuits in the living brain, we found that prefrontal spinogenesis plays a critical role in sustaining specific antidepressant behavioral effects and maintaining long-term behavioral remission. Depression-related behavior was associated with targeted, branch-specific elimination of postsynaptic dendritic spines on prefrontal projection neurons. Antidepressant-dose ketamine reversed these effects by selectively rescuing eliminated spines and restoring coordinated activity in multicellular ensembles that predict motivated escape behavior. Prefrontal spinogenesis was required for the long-term maintenance of antidepressant effects on motivated escape behavior but not for their initial induction.

Publication types

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

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology*
  • Antidepressive Agents / therapeutic use
  • Corticosterone / pharmacology
  • Dendritic Spines / drug effects*
  • Dendritic Spines / pathology
  • Dendritic Spines / physiology
  • Depressive Disorder / chemically induced
  • Depressive Disorder / drug therapy
  • Depressive Disorder / physiopathology*
  • Disease Models, Animal
  • Escape Reaction / drug effects
  • Ketamine / pharmacology*
  • Ketamine / therapeutic use
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neuronal Plasticity / drug effects
  • Prefrontal Cortex / drug effects*
  • Prefrontal Cortex / pathology
  • Prefrontal Cortex / physiopathology
  • Stress, Psychological / chemically induced
  • Stress, Psychological / physiopathology*
  • Synapses / drug effects*
  • Synapses / physiology

Substances

  • Antidepressive Agents
  • Ketamine
  • Corticosterone