Cholinergic interneurons in the nucleus accumbens regulate depression-like behavior

Proc Natl Acad Sci U S A. 2012 Jul 10;109(28):11360-5. doi: 10.1073/pnas.1209293109. Epub 2012 Jun 25.

Abstract

A large number of studies have demonstrated that the nucleus accumbens (NAC) is a critical site in the neuronal circuits controlling reward responses, motivation, and mood, but the neuronal cell type(s) underlying these processes are not yet known. Identification of the neuronal cell types that regulate depression-like states will guide us in understanding the biological basis of mood and its regulation by diseases like major depressive disorder. Taking advantage of recent findings demonstrating that the serotonin receptor chaperone, p11, is an important molecular regulator of depression-like states, here we identify cholinergic interneurons (CINs) as a primary site of action for p11 in the NAC. Depression-like behavior is observed in mice after decrease of p11 levels in NAC CINs. This phenotype is recapitulated by silencing neuronal transmission in these cells, demonstrating that accumbal cholinergic neuronal activity regulates depression-like behaviors and suggesting that accumbal CIN activity is crucial for the regulation of mood and motivation.

Publication types

  • Research Support, American Recovery and Reinvestment Act
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Annexin A2 / metabolism*
  • Antidepressive Agents / pharmacology
  • Behavior, Animal
  • Depression / metabolism
  • Depression / physiopathology*
  • Immunohistochemistry / methods
  • Interneurons / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Models, Biological
  • Molecular Chaperones / metabolism
  • Neurons / metabolism
  • Neurotransmitter Agents / metabolism
  • Nucleus Accumbens / metabolism*
  • Phenotype
  • Receptors, Cholinergic / metabolism
  • S100 Proteins / metabolism*

Substances

  • Annexin A2
  • Antidepressive Agents
  • Molecular Chaperones
  • Neurotransmitter Agents
  • Receptors, Cholinergic
  • S100 Proteins
  • S100 calcium binding protein A10
  • Acetylcholine