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Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress
BACKGROUND: The enriched environment (EE) is a laboratory housing model that emerged from efforts to minimize the impact of environmental conditions on laboratory animals. Recently, we showed that EE promoted positive effects on behavior and cortisol levels in zebrafish submitted to the unpredictabl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035866/ https://www.ncbi.nlm.nih.gov/pubmed/30002970 http://dx.doi.org/10.7717/peerj.5136 |
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author | Marcon, Matheus Mocelin, Ricieri Sachett, Adrieli Siebel, Anna M. Herrmann, Ana P. Piato, Angelo |
author_facet | Marcon, Matheus Mocelin, Ricieri Sachett, Adrieli Siebel, Anna M. Herrmann, Ana P. Piato, Angelo |
author_sort | Marcon, Matheus |
collection | PubMed |
description | BACKGROUND: The enriched environment (EE) is a laboratory housing model that emerged from efforts to minimize the impact of environmental conditions on laboratory animals. Recently, we showed that EE promoted positive effects on behavior and cortisol levels in zebrafish submitted to the unpredictable chronic stress (UCS) protocol. Here, we expanded the characterization of the effects of UCS protocol by assessing parameters of oxidative status in the zebrafish brain and reveal that EE protects against the oxidative stress induced by chronic stress. METHODS: Zebrafish were exposed to EE (21 or 28 days) or standard housing conditions and subjected to the UCS protocol for seven days. Oxidative stress parameters (lipid peroxidation (TBARS), reactive oxygen species (ROS) levels, non-protein thiol (NPSH) and total thiol (SH) levels, superoxide dismutase (SOD) and catalase (CAT) activities were measured in brain homogenate. RESULTS: Our results revealed that UCS increased lipid peroxidation and ROS levels, while decreased NPSH levels and SOD activity, suggesting oxidative damage. EE for 28 days prevented all changes induced by the UCS protocol, and EE for 21 days prevented the alterations on NPSH levels, lipid peroxidation and ROS levels. Both EE for 21 or 28 days increased CAT activity. DISCUSSION: Our findings reinforce the idea that EE exerts neuromodulatory effects in the zebrafish brain. EE promoted positive effects as it helped maintain the redox homeostasis, which may reduce the susceptibility to stress and its oxidative impact. |
format | Online Article Text |
id | pubmed-6035866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60358662018-07-12 Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress Marcon, Matheus Mocelin, Ricieri Sachett, Adrieli Siebel, Anna M. Herrmann, Ana P. Piato, Angelo PeerJ Neuroscience BACKGROUND: The enriched environment (EE) is a laboratory housing model that emerged from efforts to minimize the impact of environmental conditions on laboratory animals. Recently, we showed that EE promoted positive effects on behavior and cortisol levels in zebrafish submitted to the unpredictable chronic stress (UCS) protocol. Here, we expanded the characterization of the effects of UCS protocol by assessing parameters of oxidative status in the zebrafish brain and reveal that EE protects against the oxidative stress induced by chronic stress. METHODS: Zebrafish were exposed to EE (21 or 28 days) or standard housing conditions and subjected to the UCS protocol for seven days. Oxidative stress parameters (lipid peroxidation (TBARS), reactive oxygen species (ROS) levels, non-protein thiol (NPSH) and total thiol (SH) levels, superoxide dismutase (SOD) and catalase (CAT) activities were measured in brain homogenate. RESULTS: Our results revealed that UCS increased lipid peroxidation and ROS levels, while decreased NPSH levels and SOD activity, suggesting oxidative damage. EE for 28 days prevented all changes induced by the UCS protocol, and EE for 21 days prevented the alterations on NPSH levels, lipid peroxidation and ROS levels. Both EE for 21 or 28 days increased CAT activity. DISCUSSION: Our findings reinforce the idea that EE exerts neuromodulatory effects in the zebrafish brain. EE promoted positive effects as it helped maintain the redox homeostasis, which may reduce the susceptibility to stress and its oxidative impact. PeerJ Inc. 2018-07-05 /pmc/articles/PMC6035866/ /pubmed/30002970 http://dx.doi.org/10.7717/peerj.5136 Text en ©2018 Marcon et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Neuroscience Marcon, Matheus Mocelin, Ricieri Sachett, Adrieli Siebel, Anna M. Herrmann, Ana P. Piato, Angelo Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title | Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title_full | Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title_fullStr | Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title_full_unstemmed | Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title_short | Enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
title_sort | enriched environment prevents oxidative stress in zebrafish submitted to unpredictable chronic stress |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035866/ https://www.ncbi.nlm.nih.gov/pubmed/30002970 http://dx.doi.org/10.7717/peerj.5136 |
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