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Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma

Oxylipins play important roles in various biological processes and are considered as mediators of inflammation for a wide range of diseases such as rheumatoid arthritis (RA). The purpose of this research was to study differences in oxylipin levels between a widely used collagen induced arthritis (CI...

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Autores principales: He, Min, van Wijk, Eduard, Berger, Ruud, Wang, Mei, Strassburg, Katrin, Schoeman, Johannes C., Vreeken, Rob J., van Wietmarschen, Herman, Harms, Amy C., Kobayashi, Masaki, Hankemeier, Thomas, van der Greef, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641941/
https://www.ncbi.nlm.nih.gov/pubmed/26604432
http://dx.doi.org/10.1155/2015/543541
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author He, Min
van Wijk, Eduard
Berger, Ruud
Wang, Mei
Strassburg, Katrin
Schoeman, Johannes C.
Vreeken, Rob J.
van Wietmarschen, Herman
Harms, Amy C.
Kobayashi, Masaki
Hankemeier, Thomas
van der Greef, Jan
author_facet He, Min
van Wijk, Eduard
Berger, Ruud
Wang, Mei
Strassburg, Katrin
Schoeman, Johannes C.
Vreeken, Rob J.
van Wietmarschen, Herman
Harms, Amy C.
Kobayashi, Masaki
Hankemeier, Thomas
van der Greef, Jan
author_sort He, Min
collection PubMed
description Oxylipins play important roles in various biological processes and are considered as mediators of inflammation for a wide range of diseases such as rheumatoid arthritis (RA). The purpose of this research was to study differences in oxylipin levels between a widely used collagen induced arthritis (CIA) mice model and healthy control (Ctrl) mice. DBA/1J male mice (age: 6-7 weeks) were selected and randomly divided into two groups, namely, a CIA and a Ctrl group. The CIA mice were injected intraperitoneally (i.p.) with the joint cartilage component collagen type II (CII) and an adjuvant injection of lipopolysaccharide (LPS). Oxylipin metabolites were extracted from plasma for each individual sample using solid phase extraction (SPE) and were detected with high performance liquid chromatography/tandem mass spectrometry (HPLC-ESI-MS/MS), using dynamic multiple reaction monitoring (dMRM). Both univariate and multivariate statistical analyses were applied. The results in univariate Student's t-test revealed 10 significantly up- or downregulated oxylipins in CIA mice, which were supplemented by another 6 additional oxylipins, contributing to group clustering upon multivariate analysis. The dysregulation of these oxylipins revealed the presence of ROS-generated oxylipins and an increase of inflammation in CIA mice. The results also suggested that the collagen induced arthritis might associate with dysregulation of apoptosis, possibly inhibited by activated NF-κB because of insufficient PPAR-γ ligands.
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spelling pubmed-46419412015-11-24 Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma He, Min van Wijk, Eduard Berger, Ruud Wang, Mei Strassburg, Katrin Schoeman, Johannes C. Vreeken, Rob J. van Wietmarschen, Herman Harms, Amy C. Kobayashi, Masaki Hankemeier, Thomas van der Greef, Jan Mediators Inflamm Research Article Oxylipins play important roles in various biological processes and are considered as mediators of inflammation for a wide range of diseases such as rheumatoid arthritis (RA). The purpose of this research was to study differences in oxylipin levels between a widely used collagen induced arthritis (CIA) mice model and healthy control (Ctrl) mice. DBA/1J male mice (age: 6-7 weeks) were selected and randomly divided into two groups, namely, a CIA and a Ctrl group. The CIA mice were injected intraperitoneally (i.p.) with the joint cartilage component collagen type II (CII) and an adjuvant injection of lipopolysaccharide (LPS). Oxylipin metabolites were extracted from plasma for each individual sample using solid phase extraction (SPE) and were detected with high performance liquid chromatography/tandem mass spectrometry (HPLC-ESI-MS/MS), using dynamic multiple reaction monitoring (dMRM). Both univariate and multivariate statistical analyses were applied. The results in univariate Student's t-test revealed 10 significantly up- or downregulated oxylipins in CIA mice, which were supplemented by another 6 additional oxylipins, contributing to group clustering upon multivariate analysis. The dysregulation of these oxylipins revealed the presence of ROS-generated oxylipins and an increase of inflammation in CIA mice. The results also suggested that the collagen induced arthritis might associate with dysregulation of apoptosis, possibly inhibited by activated NF-κB because of insufficient PPAR-γ ligands. Hindawi Publishing Corporation 2015 2015-10-29 /pmc/articles/PMC4641941/ /pubmed/26604432 http://dx.doi.org/10.1155/2015/543541 Text en Copyright © 2015 Min He et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
He, Min
van Wijk, Eduard
Berger, Ruud
Wang, Mei
Strassburg, Katrin
Schoeman, Johannes C.
Vreeken, Rob J.
van Wietmarschen, Herman
Harms, Amy C.
Kobayashi, Masaki
Hankemeier, Thomas
van der Greef, Jan
Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title_full Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title_fullStr Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title_full_unstemmed Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title_short Collagen Induced Arthritis in DBA/1J Mice Associates with Oxylipin Changes in Plasma
title_sort collagen induced arthritis in dba/1j mice associates with oxylipin changes in plasma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641941/
https://www.ncbi.nlm.nih.gov/pubmed/26604432
http://dx.doi.org/10.1155/2015/543541
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