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Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats

Knowledge of animals’ hormonal status is important for conservation studies in wild or semi-free-ranging conditions as well as for behavioural and clinical experiments conducted in laboratory research, mostly performed on rats and mice. Faecal sampling is a useful non-invasive method to obtain stero...

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Autores principales: Cinque, Carlo, Zinni, Manuela, Zuena, Anna Rita, Giuli, Chiara, Alemà, Sebastiano G, Catalani, Assia, Casolini, Paola, Cozzolino, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798133/
https://www.ncbi.nlm.nih.gov/pubmed/29301863
http://dx.doi.org/10.1530/EC-17-0338
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author Cinque, Carlo
Zinni, Manuela
Zuena, Anna Rita
Giuli, Chiara
Alemà, Sebastiano G
Catalani, Assia
Casolini, Paola
Cozzolino, Roberto
author_facet Cinque, Carlo
Zinni, Manuela
Zuena, Anna Rita
Giuli, Chiara
Alemà, Sebastiano G
Catalani, Assia
Casolini, Paola
Cozzolino, Roberto
author_sort Cinque, Carlo
collection PubMed
description Knowledge of animals’ hormonal status is important for conservation studies in wild or semi-free-ranging conditions as well as for behavioural and clinical experiments conducted in laboratory research, mostly performed on rats and mice. Faecal sampling is a useful non-invasive method to obtain steroid hormone assessments. Nevertheless, in laboratory studies, unlike other contexts, faecal sampling is less utilised. One of the issues raised is the necessity to collect samples belonging to different animals, separately. Usually, researchers using faecal sampling solve this problem through the isolation of animals or taking the cage rather than single animal as unit of study. These solutions though, could lead to unreliable measurements, and cannot be applied in many studies. Our aim was to show the biological reliability of individual faecal corticosterone metabolite (FCM) assessments in socially housed male and female Wistar rats. We analytically validated the enzyme immunoassay kit used for FCM assessments. Then, we exposed the animals to two different stress stimuli that are known to activate the hypothalamus–pituitary–adrenal axis and the following release of corticosterone to biologically validate the EIA kit: environmental enrichment and predator odour. Individual faecal sampling from social animals was collected through short-time handling. The results demonstrated that both the stimuli increased FCM levels in male and female rats showing the reliability of EIA kit assessment and the applicability of our sampling method. We also found a diurnal rhythm in FCM levels. These results could help to increase the use of faecal hormone metabolite determinations in studies conducted on rats.
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spelling pubmed-57981332018-02-08 Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats Cinque, Carlo Zinni, Manuela Zuena, Anna Rita Giuli, Chiara Alemà, Sebastiano G Catalani, Assia Casolini, Paola Cozzolino, Roberto Endocr Connect Research Knowledge of animals’ hormonal status is important for conservation studies in wild or semi-free-ranging conditions as well as for behavioural and clinical experiments conducted in laboratory research, mostly performed on rats and mice. Faecal sampling is a useful non-invasive method to obtain steroid hormone assessments. Nevertheless, in laboratory studies, unlike other contexts, faecal sampling is less utilised. One of the issues raised is the necessity to collect samples belonging to different animals, separately. Usually, researchers using faecal sampling solve this problem through the isolation of animals or taking the cage rather than single animal as unit of study. These solutions though, could lead to unreliable measurements, and cannot be applied in many studies. Our aim was to show the biological reliability of individual faecal corticosterone metabolite (FCM) assessments in socially housed male and female Wistar rats. We analytically validated the enzyme immunoassay kit used for FCM assessments. Then, we exposed the animals to two different stress stimuli that are known to activate the hypothalamus–pituitary–adrenal axis and the following release of corticosterone to biologically validate the EIA kit: environmental enrichment and predator odour. Individual faecal sampling from social animals was collected through short-time handling. The results demonstrated that both the stimuli increased FCM levels in male and female rats showing the reliability of EIA kit assessment and the applicability of our sampling method. We also found a diurnal rhythm in FCM levels. These results could help to increase the use of faecal hormone metabolite determinations in studies conducted on rats. Bioscientifica Ltd 2018-01-04 /pmc/articles/PMC5798133/ /pubmed/29301863 http://dx.doi.org/10.1530/EC-17-0338 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Cinque, Carlo
Zinni, Manuela
Zuena, Anna Rita
Giuli, Chiara
Alemà, Sebastiano G
Catalani, Assia
Casolini, Paola
Cozzolino, Roberto
Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title_full Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title_fullStr Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title_full_unstemmed Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title_short Faecal corticosterone metabolite assessment in socially housed male and female Wistar rats
title_sort faecal corticosterone metabolite assessment in socially housed male and female wistar rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798133/
https://www.ncbi.nlm.nih.gov/pubmed/29301863
http://dx.doi.org/10.1530/EC-17-0338
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