NAc-VTA circuit underlies emotional stress-induced anxiety-like behavior in the three-chamber vicarious social defeat stress mouse model

Nat Commun. 2022 Jan 31;13(1):577. doi: 10.1038/s41467-022-28190-2.

Abstract

Emotional stress is considered a severe pathogenetic factor of psychiatric disorders. However, the circuit mechanisms remain largely unclear. Using a three-chamber vicarious social defeat stress (3C-VSDS) model in mice, we here show that chronic emotional stress (CES) induces anxiety-like behavior and transient social interaction changes. Dopaminergic neurons of ventral tegmental area (VTA) are required to control this behavioral deficit. VTA dopaminergic neuron hyperactivity induced by CES is involved in the anxiety-like behavior in the innate anxiogenic environment. Chemogenetic activation of VTA dopaminergic neurons directly triggers anxiety-like behavior, while chemogenetic inhibition of these neurons promotes resilience to the CES-induced anxiety-like behavior. Moreover, VTA dopaminergic neurons receiving nucleus accumbens (NAc) projections are activated in CES mice. Bidirectional modulation of the NAc-VTA circuit mimics or reverses the CES-induced anxiety-like behavior. In conclusion, we propose that a NAc-VTA circuit critically establishes and regulates the CES-induced anxiety-like behavior. This study not only characterizes a preclinical model that is representative of the nuanced aspect of CES, but also provides insight to the circuit-level neuronal processes that underlie empathy-like behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anxiety / physiopathology*
  • Behavior, Animal / physiology*
  • Dependovirus / physiology
  • Depression / physiopathology
  • Depression / psychology
  • Disease Models, Animal
  • Dopaminergic Neurons / metabolism
  • GABAergic Neurons / metabolism
  • Integrases / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neural Pathways / physiopathology*
  • Neurons / metabolism
  • Nucleus Accumbens / physiopathology*
  • Proto-Oncogene Proteins c-fos / metabolism
  • Psychological Distress*
  • Social Defeat*
  • Synapses / metabolism
  • Ventral Tegmental Area / physiopathology*
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Proto-Oncogene Proteins c-fos
  • gamma-Aminobutyric Acid
  • Cre recombinase
  • Integrases