Opposite roles for neuropeptide S in the nucleus accumbens and bed nucleus of the stria terminalis in learned helplessness rats

Behav Brain Res. 2015 Sep 15:291:67-71. doi: 10.1016/j.bbr.2015.05.007. Epub 2015 May 16.

Abstract

The role of neuropeptide S (NPS) in depression remains unclear. We examined the antidepressant-like effects of NPS infusions into the shell or core regions of the nucleus accumbens (NAc) and into the bed nucleus of the stria terminalis (BNST) of learned helplessness (LH) rats (an animal model of depression). Infusions of NPS (10 pmol/side) into the NAc shell, but not the NAc core and BNST, exerted antidepressant-like effects in the LH paradigm. Implying that behavioral deficits could be improved in the conditioned avoidance test. Coinfusion of SHA68 (an NPS receptor antagonist, 100 pmol/side) with NPS into the NAc shell blocked these effects. In contrast, NPS receptor antagonism by SHA68 in the BNST induced antidepressant-like effects. Infusions of NPS into the NAc shell or SHA68 into the BNST did not produce memory deficits or locomotor activation in the passive avoidance and open field tests. These results suggest that excitatory and inhibitory actions by the NPS system are integral to the depression in LH animals.

Keywords: Bed nucleus of the stria terminalis (BNST); Depression; Learned helplessness (LH); Neuropeptide S (NPS); Nucleus accumbens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents / administration & dosage
  • Avoidance Learning / drug effects
  • Avoidance Learning / physiology
  • Depressive Disorder / drug therapy
  • Depressive Disorder / metabolism*
  • Disease Models, Animal
  • Helplessness, Learned*
  • Male
  • Memory / drug effects
  • Memory / physiology
  • Motor Activity / drug effects
  • Motor Activity / physiology
  • Neuropeptides / administration & dosage
  • Neuropeptides / antagonists & inhibitors
  • Neuropeptides / metabolism*
  • Nucleus Accumbens / drug effects
  • Nucleus Accumbens / metabolism*
  • Oxazolidinones / pharmacology
  • Pyrazines / pharmacology
  • Rats, Sprague-Dawley
  • Receptors, Neuropeptide / antagonists & inhibitors
  • Receptors, Neuropeptide / metabolism
  • Septal Nuclei / drug effects
  • Septal Nuclei / metabolism*

Substances

  • 3-oxo-1,1-diphenyltetrahydrooxazolo(3,4-a)pyrazine-7-carboxylic acid 4-fluorobenzylamide
  • Antidepressive Agents
  • Neuropeptides
  • Oxazolidinones
  • Pyrazines
  • Receptors, Neuropeptide
  • neuropeptide S receptor, rat
  • neuropeptide S, rat