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Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats

Nesfatin-1 is a well-established anorexigenic peptide. Recent studies indicated an association between nesfatin-1 and anxiety/depression-like behavior. However, it is unclear whether this effect is retained in obesity. The aim was to investigate the effect of nesfatin-1(30-59)—the active core of nes...

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Autores principales: Kühne, Stephanie Gladys, Schalla, Martha Anna, Friedrich, Tiemo, Kobelt, Peter, Goebel-Stengel, Miriam, Long, Melissa, Rivalan, Marion, Winter, York, Rose, Matthias, Stengel, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315806/
https://www.ncbi.nlm.nih.gov/pubmed/30513901
http://dx.doi.org/10.3390/nu10121889
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author Kühne, Stephanie Gladys
Schalla, Martha Anna
Friedrich, Tiemo
Kobelt, Peter
Goebel-Stengel, Miriam
Long, Melissa
Rivalan, Marion
Winter, York
Rose, Matthias
Stengel, Andreas
author_facet Kühne, Stephanie Gladys
Schalla, Martha Anna
Friedrich, Tiemo
Kobelt, Peter
Goebel-Stengel, Miriam
Long, Melissa
Rivalan, Marion
Winter, York
Rose, Matthias
Stengel, Andreas
author_sort Kühne, Stephanie Gladys
collection PubMed
description Nesfatin-1 is a well-established anorexigenic peptide. Recent studies indicated an association between nesfatin-1 and anxiety/depression-like behavior. However, it is unclear whether this effect is retained in obesity. The aim was to investigate the effect of nesfatin-1(30-59)—the active core of nesfatin-1—on anxiety and depression-like behavior in normal weight (NW) and diet-induced (DIO) obese rats. Male rats were intracerebroventricularly (ICV) cannulated and received nesfatin-1(30-59) (0.1, 0.3, or 0.9 nmol/rat) or vehicle 30 min before testing. Nesfatin-1(30-59) at a dose of 0.3 nmol reduced sucrose consumption in the sucrose preference test in NW rats compared to vehicle (–33%, p < 0.05), indicating depression-like/anhedonic behavior. This dose was used for all following experiments. Nesfatin-1(30-59) also reduced cookie intake during the novelty-induced hypophagia test (−62%, p < 0.05). Moreover, nesfatin-1(30-59) reduced the number of entries into the center zone in the open field test (−45%, p < 0.01) and the visits of open arms in the elevated zero maze test (−39%, p < 0.01) in NW rats indicating anxiety. Interestingly, DIO rats showed no behavioral alterations after the injection of nesfatin-1(30-59) (p > 0.05). These results indicate an implication of nesfatin-1(30-59) in the mediation of anxiety and depression-like behavior/anhedonia under normal weight conditions, while in DIO rats, a desensitization might occur.
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spelling pubmed-63158062019-01-08 Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats Kühne, Stephanie Gladys Schalla, Martha Anna Friedrich, Tiemo Kobelt, Peter Goebel-Stengel, Miriam Long, Melissa Rivalan, Marion Winter, York Rose, Matthias Stengel, Andreas Nutrients Article Nesfatin-1 is a well-established anorexigenic peptide. Recent studies indicated an association between nesfatin-1 and anxiety/depression-like behavior. However, it is unclear whether this effect is retained in obesity. The aim was to investigate the effect of nesfatin-1(30-59)—the active core of nesfatin-1—on anxiety and depression-like behavior in normal weight (NW) and diet-induced (DIO) obese rats. Male rats were intracerebroventricularly (ICV) cannulated and received nesfatin-1(30-59) (0.1, 0.3, or 0.9 nmol/rat) or vehicle 30 min before testing. Nesfatin-1(30-59) at a dose of 0.3 nmol reduced sucrose consumption in the sucrose preference test in NW rats compared to vehicle (–33%, p < 0.05), indicating depression-like/anhedonic behavior. This dose was used for all following experiments. Nesfatin-1(30-59) also reduced cookie intake during the novelty-induced hypophagia test (−62%, p < 0.05). Moreover, nesfatin-1(30-59) reduced the number of entries into the center zone in the open field test (−45%, p < 0.01) and the visits of open arms in the elevated zero maze test (−39%, p < 0.01) in NW rats indicating anxiety. Interestingly, DIO rats showed no behavioral alterations after the injection of nesfatin-1(30-59) (p > 0.05). These results indicate an implication of nesfatin-1(30-59) in the mediation of anxiety and depression-like behavior/anhedonia under normal weight conditions, while in DIO rats, a desensitization might occur. MDPI 2018-12-01 /pmc/articles/PMC6315806/ /pubmed/30513901 http://dx.doi.org/10.3390/nu10121889 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kühne, Stephanie Gladys
Schalla, Martha Anna
Friedrich, Tiemo
Kobelt, Peter
Goebel-Stengel, Miriam
Long, Melissa
Rivalan, Marion
Winter, York
Rose, Matthias
Stengel, Andreas
Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title_full Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title_fullStr Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title_full_unstemmed Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title_short Nesfatin-1(30-59) Injected Intracerebroventricularly Increases Anxiety, Depression-Like Behavior, and Anhedonia in Normal Weight Rats
title_sort nesfatin-1(30-59) injected intracerebroventricularly increases anxiety, depression-like behavior, and anhedonia in normal weight rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315806/
https://www.ncbi.nlm.nih.gov/pubmed/30513901
http://dx.doi.org/10.3390/nu10121889
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