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Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress

Restraint stress (RS) is a condition affecting millions of people worldwide. The investigation of new therapies to alleviate the consequences of prolonged RS is much needed. Cotinine, a nicotine-derivative, has shown to prevent the decrease in cerebral synaptic density, working memory deficits, anxi...

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Autores principales: Mendoza, Cristhian, Perez-Urrutia, Nelson, Alvarez-Ricartes, Nathalie, Barreto, George E., Pérez-Ordás, Raquel, Iarkov, Alex, Echeverria, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305112/
https://www.ncbi.nlm.nih.gov/pubmed/30618579
http://dx.doi.org/10.3389/fnins.2018.00952
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author Mendoza, Cristhian
Perez-Urrutia, Nelson
Alvarez-Ricartes, Nathalie
Barreto, George E.
Pérez-Ordás, Raquel
Iarkov, Alex
Echeverria, Valentina
author_facet Mendoza, Cristhian
Perez-Urrutia, Nelson
Alvarez-Ricartes, Nathalie
Barreto, George E.
Pérez-Ordás, Raquel
Iarkov, Alex
Echeverria, Valentina
author_sort Mendoza, Cristhian
collection PubMed
description Restraint stress (RS) is a condition affecting millions of people worldwide. The investigation of new therapies to alleviate the consequences of prolonged RS is much needed. Cotinine, a nicotine-derivative, has shown to prevent the decrease in cerebral synaptic density, working memory deficits, anxiety, and depressive-like behavior after prolonged restraint stress (RS) in mice. Furthermore, post-treatment with cotinine reduced the adverse effects of chronic RS on astrocyte survival and architecture. On the other hand, the nutritional supplement krill oil (KO), has shown to be beneficial in decreasing depressive-like behavior and oxidative stress. In this study, in the search for effective preventative treatments to be used in people subjected to reduced mobility, the effect of co-treatment with cotinine plus KO in mice subjected to prolonged RS was investigated. The results show that cotinine plus KO prevented the loss of astrocytes, the appearance of depressive-like behavior and cognitive impairment induced by RS. The use of the combination of cotinine plus KO was more effective than cotinine alone in preventing the depressive-like behavior in the restrained mice. The potential use of this combination to alleviate the psychological effects of reduced mobility is discussed.
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spelling pubmed-63051122019-01-07 Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress Mendoza, Cristhian Perez-Urrutia, Nelson Alvarez-Ricartes, Nathalie Barreto, George E. Pérez-Ordás, Raquel Iarkov, Alex Echeverria, Valentina Front Neurosci Neuroscience Restraint stress (RS) is a condition affecting millions of people worldwide. The investigation of new therapies to alleviate the consequences of prolonged RS is much needed. Cotinine, a nicotine-derivative, has shown to prevent the decrease in cerebral synaptic density, working memory deficits, anxiety, and depressive-like behavior after prolonged restraint stress (RS) in mice. Furthermore, post-treatment with cotinine reduced the adverse effects of chronic RS on astrocyte survival and architecture. On the other hand, the nutritional supplement krill oil (KO), has shown to be beneficial in decreasing depressive-like behavior and oxidative stress. In this study, in the search for effective preventative treatments to be used in people subjected to reduced mobility, the effect of co-treatment with cotinine plus KO in mice subjected to prolonged RS was investigated. The results show that cotinine plus KO prevented the loss of astrocytes, the appearance of depressive-like behavior and cognitive impairment induced by RS. The use of the combination of cotinine plus KO was more effective than cotinine alone in preventing the depressive-like behavior in the restrained mice. The potential use of this combination to alleviate the psychological effects of reduced mobility is discussed. Frontiers Media S.A. 2018-12-17 /pmc/articles/PMC6305112/ /pubmed/30618579 http://dx.doi.org/10.3389/fnins.2018.00952 Text en Copyright © 2018 Mendoza, Perez-Urrutia, Alvarez-Ricartes, Barreto, Pérez-Ordás, Iarkov and Echeverria. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Mendoza, Cristhian
Perez-Urrutia, Nelson
Alvarez-Ricartes, Nathalie
Barreto, George E.
Pérez-Ordás, Raquel
Iarkov, Alex
Echeverria, Valentina
Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title_full Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title_fullStr Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title_full_unstemmed Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title_short Cotinine Plus Krill Oil Decreased Depressive Behavior, and Increased Astrocytes Survival in the Hippocampus of Mice Subjected to Restraint Stress
title_sort cotinine plus krill oil decreased depressive behavior, and increased astrocytes survival in the hippocampus of mice subjected to restraint stress
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305112/
https://www.ncbi.nlm.nih.gov/pubmed/30618579
http://dx.doi.org/10.3389/fnins.2018.00952
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