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Wegener, G. ; Finger, B. ; Elfving, B. ; Keller, K. ; Liebenberg, N. ; Fischer, C. W. ; Singewald, N. ; Slattery, David A. ; Neumann, Inga D. ; Mathé, A. A.

Neuropeptide S alters anxiety, but not depression-like behaviour in Flinders Sensitive Line rats: a genetic animal model of depression

Wegener, G. , Finger, B., Elfving, B. , Keller, K., Liebenberg, N. , Fischer, C. W., Singewald, N. , Slattery, David A., Neumann, Inga D. and Mathé, A. A. (2012) Neuropeptide S alters anxiety, but not depression-like behaviour in Flinders Sensitive Line rats: a genetic animal model of depression. International Journal of Neuropsychopharmacology 15, pp. 375-387.

Date of publication of this fulltext: 06 Oct 2016 14:41
Article
DOI to cite this document: 10.5283/epub.34579


Abstract

Neuropeptide S (NPS) and its receptor (NPSR) have been implicated in the mediation of anxiolytic-like behaviour in rodents. However, little knowledge is available regarding the NPS system in depression-related behaviours, and whether NPS also exerts anxiolytic effects in an animal model of psychopathology. Therefore, the aim of this work was to characterize the effects of NPS on depression-and ...

Neuropeptide S (NPS) and its receptor (NPSR) have been implicated in the mediation of anxiolytic-like behaviour in rodents. However, little knowledge is available regarding the NPS system in depression-related behaviours, and whether NPS also exerts anxiolytic effects in an animal model of psychopathology. Therefore, the aim of this work was to characterize the effects of NPS on depression-and anxiety-related parameters, using male and female rats in a well-validated animal model of depression: the Flinders Sensitive Line (FSL), their controls, the Flinders Resistant Line (FRL), and Sprague-Dawley (SD) rats. We found that FSL showed greater immobility in the forced swim test (FST) than FRL, confirming their phenotype. However, NPS did not affect depression-related behaviour in any rat line. No significant differences in baseline anxiety levels between the FSL and FRL strains were observed, but FSL and FRL rats displayed less anxiety-like behaviour compared to SD rats. NPS decreased anxiety-like behaviour on the elevated plus-maze in all strains. The expression of the NPSR in the amygdala, peri-ventricular hypothalamic nucleus, and hippocampus was equal in all male strains, although a trend towards reduced expression within the amygdala was observed in FSL rats compared to SD rats. In conclusion, NPS had a marked anxiolytic effect in FSL, FRL and SD rats, but did not modify the depression-related behaviour in any strain, in spite of the significant differences in innate level between the strains. These findings suggest that NPS specifically modifies anxiety behaviour but cannot overcome/reverse a genetically mediated depression phenotype.



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Details

Item typeArticle
Journal or Publication TitleInternational Journal of Neuropsychopharmacology
Publisher:CAMBRIDGE UNIV PRESS
Open Access Type:Alliance-/National licence
Place of Publication:NEW YORK
Volume:15
Page Range:pp. 375-387
Date2012
InstitutionsBiology, Preclinical Medicine > Institut für Zoologie > Tierphysiologie/Neurobiologie (Prof. Dr. Inga Neumann)
Identification Number
ValueType
10.1017/S1461145711000678DOI
KeywordsRECEPTOR ANTAGONISTS; ELECTROCONVULSIVE STIMULI; UNIPOLAR DEPRESSION; VERBAL MEMORY; FOOD-INTAKE; ANTIDEPRESSANTS; MICE; HIPPOCAMPUS; SYSTEM; BRAIN; Animal model; anxiety; gene expression; depression; NPS
Dewey Decimal Classification500 Science > 590 Zoological sciences
500 Science > 590 Zoological sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-345795
Item ID34579

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