Cargando…
Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry
The aquaculture industry has become a sustainable source of food for humans. Remaining challenges include disease issues and ethical concerns for the discomfort and stress of farmed fish. There is a need for reliable biomarkers to monitor welfare in fish, and the stress hormone cortisol has been sug...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031784/ https://www.ncbi.nlm.nih.gov/pubmed/35458678 http://dx.doi.org/10.3390/molecules27082481 |
_version_ | 1784692477433741312 |
---|---|
author | Meling, Vanessa Andrea Berge, Kjetil Knudsen, David Lausten Rønning, Per Ola Brede, Cato |
author_facet | Meling, Vanessa Andrea Berge, Kjetil Knudsen, David Lausten Rønning, Per Ola Brede, Cato |
author_sort | Meling, Vanessa Andrea |
collection | PubMed |
description | The aquaculture industry has become a sustainable source of food for humans. Remaining challenges include disease issues and ethical concerns for the discomfort and stress of farmed fish. There is a need for reliable biomarkers to monitor welfare in fish, and the stress hormone cortisol has been suggested as a good candidate. This study presents a novel method for measurement of cortisol in fish feces based on enzymatic hydrolysis, liquid–liquid extraction, derivatization, and finally instrumental analysis by liquid chromatography coupled with tandem mass spectrometry. Hydrolysis and extraction conditions were optimized. Cortisol appeared to be mostly conjugated to sulfate and less conjugated to glucuronic acid in the studied samples of feces from farmed Atlantic salmon. The method was suitable for quantification of cortisol after enzymatic deconjugation by either combined glucuronidase and sulfatase activity, or by glucuronidase activity alone. The limit of detection was 0.15 ng/g, the limit of quantification was 0.34 ng/g, and the method was linear (R(2) > 0.997) up to 380 ng/g, for measurement of cortisol in wet feces. Method repeatability and intermediate precision were acceptable, both with a coefficient of variation (CV) of 11%. Stress level was high in fish released into seawater, and significantly reduced after eight days. |
format | Online Article Text |
id | pubmed-9031784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90317842022-04-23 Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry Meling, Vanessa Andrea Berge, Kjetil Knudsen, David Lausten Rønning, Per Ola Brede, Cato Molecules Article The aquaculture industry has become a sustainable source of food for humans. Remaining challenges include disease issues and ethical concerns for the discomfort and stress of farmed fish. There is a need for reliable biomarkers to monitor welfare in fish, and the stress hormone cortisol has been suggested as a good candidate. This study presents a novel method for measurement of cortisol in fish feces based on enzymatic hydrolysis, liquid–liquid extraction, derivatization, and finally instrumental analysis by liquid chromatography coupled with tandem mass spectrometry. Hydrolysis and extraction conditions were optimized. Cortisol appeared to be mostly conjugated to sulfate and less conjugated to glucuronic acid in the studied samples of feces from farmed Atlantic salmon. The method was suitable for quantification of cortisol after enzymatic deconjugation by either combined glucuronidase and sulfatase activity, or by glucuronidase activity alone. The limit of detection was 0.15 ng/g, the limit of quantification was 0.34 ng/g, and the method was linear (R(2) > 0.997) up to 380 ng/g, for measurement of cortisol in wet feces. Method repeatability and intermediate precision were acceptable, both with a coefficient of variation (CV) of 11%. Stress level was high in fish released into seawater, and significantly reduced after eight days. MDPI 2022-04-12 /pmc/articles/PMC9031784/ /pubmed/35458678 http://dx.doi.org/10.3390/molecules27082481 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Meling, Vanessa Andrea Berge, Kjetil Knudsen, David Lausten Rønning, Per Ola Brede, Cato Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title | Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title_full | Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title_fullStr | Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title_full_unstemmed | Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title_short | Monitoring Farmed Fish Welfare by Measurement of Cortisol as a Stress Marker in Fish Feces by Liquid Chromatography Coupled with Tandem Mass Spectrometry |
title_sort | monitoring farmed fish welfare by measurement of cortisol as a stress marker in fish feces by liquid chromatography coupled with tandem mass spectrometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031784/ https://www.ncbi.nlm.nih.gov/pubmed/35458678 http://dx.doi.org/10.3390/molecules27082481 |
work_keys_str_mv | AT melingvanessaandrea monitoringfarmedfishwelfarebymeasurementofcortisolasastressmarkerinfishfecesbyliquidchromatographycoupledwithtandemmassspectrometry AT bergekjetil monitoringfarmedfishwelfarebymeasurementofcortisolasastressmarkerinfishfecesbyliquidchromatographycoupledwithtandemmassspectrometry AT knudsendavidlausten monitoringfarmedfishwelfarebymeasurementofcortisolasastressmarkerinfishfecesbyliquidchromatographycoupledwithtandemmassspectrometry AT rønningperola monitoringfarmedfishwelfarebymeasurementofcortisolasastressmarkerinfishfecesbyliquidchromatographycoupledwithtandemmassspectrometry AT bredecato monitoringfarmedfishwelfarebymeasurementofcortisolasastressmarkerinfishfecesbyliquidchromatographycoupledwithtandemmassspectrometry |