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Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair
The measurement of naturally occurring glucocorticoids and stable isotopes of several elements has gained importance in wildlife studies in recent decades and opened a myriad of ecological applications. Cortisol and stable isotopes equilibrate in animal tissues over periods of integration related to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569930/ https://www.ncbi.nlm.nih.gov/pubmed/28852516 http://dx.doi.org/10.1093/conphys/cox021 |
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author | Sergiel, Agnieszka Hobson, Keith A. Janz, David M. Cattet, Marc Selva, Nuria Kapronczai, Luciene Gryba, Chantel Zedrosser, Andreas |
author_facet | Sergiel, Agnieszka Hobson, Keith A. Janz, David M. Cattet, Marc Selva, Nuria Kapronczai, Luciene Gryba, Chantel Zedrosser, Andreas |
author_sort | Sergiel, Agnieszka |
collection | PubMed |
description | The measurement of naturally occurring glucocorticoids and stable isotopes of several elements has gained importance in wildlife studies in recent decades and opened a myriad of ecological applications. Cortisol and stable isotopes equilibrate in animal tissues over periods of integration related to the growth rate of the tissue, providing information reflecting systemic cortisol secretion and dietary intake. Sample preparation shares the common step of first cleaning the sample of external contamination. However, it is not well understood how different solvents used in sample preparation affect isotopic and cortisol values, and whether it is safe to follow the same procedures for both measures to optimize analyses of the same sample. We conducted an experiment to compare different preparation protocols for the analysis of cortisol concentrations and stable carbon (δ(13)C) and nitrogen (δ(15)N) isotope ratios in hair. Hair samples from 12 brown bears (Ursus arctos) were each divided into five aliquots; two aliquots were rinsed with a 2:1 chloroform:methanol (v/v) mixture with one aliquot ground prior to cortisol analysis and the other left intact for stable isotope analyses; two aliquots were washed with methanol with one aliquot ground prior to cortisol analysis and the other left intact for stable isotope analyses; and one aliquot washed with methanol and ground prior to stable isotope analyses. The cortisol, δ(13)C and δ(15)N values remained consistent following all treatments. Our results indicate that hair samples rinsed with a 2:1 chloroform:methanol mixture or washed with methanol can be used for both types of analyses. Further, hair that has been ground in a standard hair cortisol procedure can also be used for stable isotope analysis. This information is important for improving laboratory efficiency and compatibility of procedures used for wildlife physiological ecology studies where concurrent measurements of cortisol and stable isotopes in hair are required. |
format | Online Article Text |
id | pubmed-5569930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55699302017-08-29 Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair Sergiel, Agnieszka Hobson, Keith A. Janz, David M. Cattet, Marc Selva, Nuria Kapronczai, Luciene Gryba, Chantel Zedrosser, Andreas Conserv Physiol Toolbox The measurement of naturally occurring glucocorticoids and stable isotopes of several elements has gained importance in wildlife studies in recent decades and opened a myriad of ecological applications. Cortisol and stable isotopes equilibrate in animal tissues over periods of integration related to the growth rate of the tissue, providing information reflecting systemic cortisol secretion and dietary intake. Sample preparation shares the common step of first cleaning the sample of external contamination. However, it is not well understood how different solvents used in sample preparation affect isotopic and cortisol values, and whether it is safe to follow the same procedures for both measures to optimize analyses of the same sample. We conducted an experiment to compare different preparation protocols for the analysis of cortisol concentrations and stable carbon (δ(13)C) and nitrogen (δ(15)N) isotope ratios in hair. Hair samples from 12 brown bears (Ursus arctos) were each divided into five aliquots; two aliquots were rinsed with a 2:1 chloroform:methanol (v/v) mixture with one aliquot ground prior to cortisol analysis and the other left intact for stable isotope analyses; two aliquots were washed with methanol with one aliquot ground prior to cortisol analysis and the other left intact for stable isotope analyses; and one aliquot washed with methanol and ground prior to stable isotope analyses. The cortisol, δ(13)C and δ(15)N values remained consistent following all treatments. Our results indicate that hair samples rinsed with a 2:1 chloroform:methanol mixture or washed with methanol can be used for both types of analyses. Further, hair that has been ground in a standard hair cortisol procedure can also be used for stable isotope analysis. This information is important for improving laboratory efficiency and compatibility of procedures used for wildlife physiological ecology studies where concurrent measurements of cortisol and stable isotopes in hair are required. Oxford University Press 2017-03-24 /pmc/articles/PMC5569930/ /pubmed/28852516 http://dx.doi.org/10.1093/conphys/cox021 Text en © The Author 2017. Published by Oxford University Press and the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Toolbox Sergiel, Agnieszka Hobson, Keith A. Janz, David M. Cattet, Marc Selva, Nuria Kapronczai, Luciene Gryba, Chantel Zedrosser, Andreas Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title | Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title_full | Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title_fullStr | Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title_full_unstemmed | Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title_short | Compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)C, δ(15)N) ratios: a test on brown bear hair |
title_sort | compatibility of preparatory procedures for the analysis of cortisol concentrations and stable isotope (δ(13)c, δ(15)n) ratios: a test on brown bear hair |
topic | Toolbox |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569930/ https://www.ncbi.nlm.nih.gov/pubmed/28852516 http://dx.doi.org/10.1093/conphys/cox021 |
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