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Alterations to oxidative stress markers in dogs after a short-term stress during transport

While methods to evaluate antioxidant capacity in animals exist, one problem with the models is induction of oxidative stress. It is necessary to promote a great enough challenge to induce measurable alterations to oxidative parameters while ensuring the protocol is compatible with animal welfare. T...

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Autores principales: Ferreira, Chayanne S., Vasconcellos, Ricardo S., Pedreira, Raquel S., Silva, Flavio L., Sá, Fabiano C., Kroll, Fernanda S. A., Maria, Ana P. J., Venturini, Katiani S., Carciofi, Aulus C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473139/
https://www.ncbi.nlm.nih.gov/pubmed/26101596
http://dx.doi.org/10.1017/jns.2014.47
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author Ferreira, Chayanne S.
Vasconcellos, Ricardo S.
Pedreira, Raquel S.
Silva, Flavio L.
Sá, Fabiano C.
Kroll, Fernanda S. A.
Maria, Ana P. J.
Venturini, Katiani S.
Carciofi, Aulus C.
author_facet Ferreira, Chayanne S.
Vasconcellos, Ricardo S.
Pedreira, Raquel S.
Silva, Flavio L.
Sá, Fabiano C.
Kroll, Fernanda S. A.
Maria, Ana P. J.
Venturini, Katiani S.
Carciofi, Aulus C.
author_sort Ferreira, Chayanne S.
collection PubMed
description While methods to evaluate antioxidant capacity in animals exist, one problem with the models is induction of oxidative stress. It is necessary to promote a great enough challenge to induce measurable alterations to oxidative parameters while ensuring the protocol is compatible with animal welfare. The aim of the present study was to evaluate caged transport as a viable short-term stress that would significantly affect oxidative parameters. Twenty adult Beagle dogs, maintained on the same diet for 60 d prior to the transport, were included in the study. To simulate the stress, the dogs were housed in pairs in transport cages (1·0 m × 1·0 m × 1·5 m), placed on a truck coupled to a trailer and transported for a period of 15 min. Blood collection was performed immediately before and again 3 h after the transportation to evaluate oxidative parameters in blood serum, including thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), sequestration activity of the radical 2,2-diphenyl-1-picryl-hydrazyl (DPPH•), protein carbonylation (PC), total sulfhydryl groups (SH), alpha-tocopherol (αToc) and retinol (Ret). PC, SH and αToc were not significantly changed in the study; however, TBARS, TAC and DPPH increased, whereas Ret decreased after the transport. Although the lack of a control group of dogs not submitted to transport is a limitation to be considered, we conclude that the transport model is effective in inducing an antioxidant response in dogs and relevant blood parameters show sensitivity to this proposed model.
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spelling pubmed-44731392015-06-22 Alterations to oxidative stress markers in dogs after a short-term stress during transport Ferreira, Chayanne S. Vasconcellos, Ricardo S. Pedreira, Raquel S. Silva, Flavio L. Sá, Fabiano C. Kroll, Fernanda S. A. Maria, Ana P. J. Venturini, Katiani S. Carciofi, Aulus C. J Nutr Sci WALTHAM Supplement While methods to evaluate antioxidant capacity in animals exist, one problem with the models is induction of oxidative stress. It is necessary to promote a great enough challenge to induce measurable alterations to oxidative parameters while ensuring the protocol is compatible with animal welfare. The aim of the present study was to evaluate caged transport as a viable short-term stress that would significantly affect oxidative parameters. Twenty adult Beagle dogs, maintained on the same diet for 60 d prior to the transport, were included in the study. To simulate the stress, the dogs were housed in pairs in transport cages (1·0 m × 1·0 m × 1·5 m), placed on a truck coupled to a trailer and transported for a period of 15 min. Blood collection was performed immediately before and again 3 h after the transportation to evaluate oxidative parameters in blood serum, including thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), sequestration activity of the radical 2,2-diphenyl-1-picryl-hydrazyl (DPPH•), protein carbonylation (PC), total sulfhydryl groups (SH), alpha-tocopherol (αToc) and retinol (Ret). PC, SH and αToc were not significantly changed in the study; however, TBARS, TAC and DPPH increased, whereas Ret decreased after the transport. Although the lack of a control group of dogs not submitted to transport is a limitation to be considered, we conclude that the transport model is effective in inducing an antioxidant response in dogs and relevant blood parameters show sensitivity to this proposed model. Cambridge University Press 2014-09-25 /pmc/articles/PMC4473139/ /pubmed/26101596 http://dx.doi.org/10.1017/jns.2014.47 Text en © The Author(s) 2014 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution license <http://creativecommons.org/licenses/by/3.0/.
spellingShingle WALTHAM Supplement
Ferreira, Chayanne S.
Vasconcellos, Ricardo S.
Pedreira, Raquel S.
Silva, Flavio L.
Sá, Fabiano C.
Kroll, Fernanda S. A.
Maria, Ana P. J.
Venturini, Katiani S.
Carciofi, Aulus C.
Alterations to oxidative stress markers in dogs after a short-term stress during transport
title Alterations to oxidative stress markers in dogs after a short-term stress during transport
title_full Alterations to oxidative stress markers in dogs after a short-term stress during transport
title_fullStr Alterations to oxidative stress markers in dogs after a short-term stress during transport
title_full_unstemmed Alterations to oxidative stress markers in dogs after a short-term stress during transport
title_short Alterations to oxidative stress markers in dogs after a short-term stress during transport
title_sort alterations to oxidative stress markers in dogs after a short-term stress during transport
topic WALTHAM Supplement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473139/
https://www.ncbi.nlm.nih.gov/pubmed/26101596
http://dx.doi.org/10.1017/jns.2014.47
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