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Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma

BACKGROUND: Studies have reported that heparin may be unsuitable as an anticoagulant in human plasma samples when quantifying cytokines using multiplex bead array assays. For mouse samples, multiplex assays have been validated for serum and EDTA-plasma, but it remains to be elucidated whether hepari...

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Autores principales: Teilmann, Anne C, Kalliokoski, Otto, Jacobsen, Kirsten R, Hau, Jann, Abelson, Klas SP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041355/
https://www.ncbi.nlm.nih.gov/pubmed/24884817
http://dx.doi.org/10.1186/1751-0147-56-33
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author Teilmann, Anne C
Kalliokoski, Otto
Jacobsen, Kirsten R
Hau, Jann
Abelson, Klas SP
author_facet Teilmann, Anne C
Kalliokoski, Otto
Jacobsen, Kirsten R
Hau, Jann
Abelson, Klas SP
author_sort Teilmann, Anne C
collection PubMed
description BACKGROUND: Studies have reported that heparin may be unsuitable as an anticoagulant in human plasma samples when quantifying cytokines using multiplex bead array assays. For mouse samples, multiplex assays have been validated for serum and EDTA-plasma, but it remains to be elucidated whether heparin influences the quantification of cytokines, and if so – to what extent. Furthermore, laboratory mice are often anesthetized for blood sampling, which causes acute stress that may influence circulating cytokine concentrations and thus bias experimental results. The objectives of the present study were to identify whether specific cytokine concentrations varied between heparin-plasma, serum, and EDTA-plasma, and whether short isoflurane anesthesia would influence the concentrations of these cytokines in the circulation. Twenty-three acute phase and pro-inflammatory cytokines were quantified in matched serum, EDTA-plasma, and heparin-plasma samples from anesthetized and unanesthetized male NMRI mice using a multiplex assay. In addition, samples from unanesthetized mice were spiked with three levels of heparin. RESULTS: The concentrations of five out of 23 cytokines were significantly different between sample types, but only one cytokine (IL-17A) differed between heparin-plasma and serum. When further spiking the heparin-plasma with increasing concentrations of heparin, there was a significant effect on 11 cytokines, where the cytokine recovery could be correlated to the heparin concentration for ten of these cytokines. Anesthesia resulted in lower concentrations of G-CSF, but had no significant impact on the concentrations of the other 22 cytokines. CONCLUSION: In mice, heparin seems like a suitable anticoagulant for obtaining plasma for multiplex assays for the cytokines IL-1α, IL-1β, IL-2, IL-6, IL-9, IL-12p40, IL-12p70, IL-13, G-CSF, GM-CSF, IFN-γ, KC, MCP-1, MIP-1α, MIP-1β, RANTES and TNFα, but an effect of heparin in high concentrations should be considered for the cytokines IL-9, IL-12p40, IL-12p70, KC, MCP-1, MIP-1β and RANTES. Short isoflurane anesthesia had significant impact on G-CSF, but none of the other cytokines.
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spelling pubmed-40413552014-06-16 Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma Teilmann, Anne C Kalliokoski, Otto Jacobsen, Kirsten R Hau, Jann Abelson, Klas SP Acta Vet Scand Research BACKGROUND: Studies have reported that heparin may be unsuitable as an anticoagulant in human plasma samples when quantifying cytokines using multiplex bead array assays. For mouse samples, multiplex assays have been validated for serum and EDTA-plasma, but it remains to be elucidated whether heparin influences the quantification of cytokines, and if so – to what extent. Furthermore, laboratory mice are often anesthetized for blood sampling, which causes acute stress that may influence circulating cytokine concentrations and thus bias experimental results. The objectives of the present study were to identify whether specific cytokine concentrations varied between heparin-plasma, serum, and EDTA-plasma, and whether short isoflurane anesthesia would influence the concentrations of these cytokines in the circulation. Twenty-three acute phase and pro-inflammatory cytokines were quantified in matched serum, EDTA-plasma, and heparin-plasma samples from anesthetized and unanesthetized male NMRI mice using a multiplex assay. In addition, samples from unanesthetized mice were spiked with three levels of heparin. RESULTS: The concentrations of five out of 23 cytokines were significantly different between sample types, but only one cytokine (IL-17A) differed between heparin-plasma and serum. When further spiking the heparin-plasma with increasing concentrations of heparin, there was a significant effect on 11 cytokines, where the cytokine recovery could be correlated to the heparin concentration for ten of these cytokines. Anesthesia resulted in lower concentrations of G-CSF, but had no significant impact on the concentrations of the other 22 cytokines. CONCLUSION: In mice, heparin seems like a suitable anticoagulant for obtaining plasma for multiplex assays for the cytokines IL-1α, IL-1β, IL-2, IL-6, IL-9, IL-12p40, IL-12p70, IL-13, G-CSF, GM-CSF, IFN-γ, KC, MCP-1, MIP-1α, MIP-1β, RANTES and TNFα, but an effect of heparin in high concentrations should be considered for the cytokines IL-9, IL-12p40, IL-12p70, KC, MCP-1, MIP-1β and RANTES. Short isoflurane anesthesia had significant impact on G-CSF, but none of the other cytokines. BioMed Central 2014-05-20 /pmc/articles/PMC4041355/ /pubmed/24884817 http://dx.doi.org/10.1186/1751-0147-56-33 Text en Copyright © 2014 Teilmann et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Teilmann, Anne C
Kalliokoski, Otto
Jacobsen, Kirsten R
Hau, Jann
Abelson, Klas SP
Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title_full Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title_fullStr Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title_full_unstemmed Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title_short Impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
title_sort impact of heparin and short term anesthesia on the quantification of cytokines in laboratory mouse plasma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041355/
https://www.ncbi.nlm.nih.gov/pubmed/24884817
http://dx.doi.org/10.1186/1751-0147-56-33
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