Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages
Cyclooxygenase 2 (COX-2) plays a key role in the regulation of inflammation by catalyzing the oxygenation of PUFAs to prostaglandins (PGs) and hydroperoxides. Next to this, COX-2 can metabolize neutral lipids, including endocannabinoid-like esters and amides. We developed an LC-HRMS-based human recombinant (h)COX-2 screening assay to examine its ability to also convert n-3 PUFA-derived N-acylethanolamines. Our assay yields known hCOX-2-derived products from established PUFAs and anandamide. Subsequently, we proved that eicosapentaenoylethanolamide (EPEA), the N-acylethanolamine derivative of EPA, is converted into PGE3-ethanolamide (PGE3-EA), and into 11-, 14-, and 18-hydroxyeicosapentaenoyl-EA (11-, 14-, and 18-HEPE-EA, respectively). Interestingly, we demonstrated that docosahexaenoylethanolamide (DHEA) is converted by hCOX-2 into the previously unknown metabolites, 13- and 16-hydroxy-DHEA (13- and 16-HDHEA, respectively). These products were also produced by lipopolysaccharide-stimulated RAW267.4 macrophages incubated with DHEA. No oxygenated DHEA metabolites were detected when the selective COX-2 inhibitor, celecoxib, was added to the cells, further underlining the role of COX-2 in the formation of the novel hydroxylated products. This work demonstrates for the first time that DHEA and EPEA are converted by COX-2 into previously unknown hydroxylated metabolites and invites future studies toward the biological effects of these metabolites.
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Format: | Article/Letter to editor biblioteca |
Language: | English |
Subjects: | cyclooxygenase, cyclooxygenase 2, fatty acid amides, fatty acid oxidation, high-performance liquid chromatography, inflammation, mass spectrometry, prostaglandins, |
Online Access: | https://research.wur.nl/en/publications/novel-cox-2-products-of-n-3-polyunsaturated-fatty-acid-ethanolami |
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dig-wur-nl-wurpubs-5559452025-01-16 de Bus, Ian Zuilhof, Han Witkamp, Renger Balvers, Michiel Albada, Bauke Article/Letter to editor Journal of Lipid Research 60 (2019) 11 ISSN: 0022-2275 Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages 2019 Cyclooxygenase 2 (COX-2) plays a key role in the regulation of inflammation by catalyzing the oxygenation of PUFAs to prostaglandins (PGs) and hydroperoxides. Next to this, COX-2 can metabolize neutral lipids, including endocannabinoid-like esters and amides. We developed an LC-HRMS-based human recombinant (h)COX-2 screening assay to examine its ability to also convert n-3 PUFA-derived N-acylethanolamines. Our assay yields known hCOX-2-derived products from established PUFAs and anandamide. Subsequently, we proved that eicosapentaenoylethanolamide (EPEA), the N-acylethanolamine derivative of EPA, is converted into PGE3-ethanolamide (PGE3-EA), and into 11-, 14-, and 18-hydroxyeicosapentaenoyl-EA (11-, 14-, and 18-HEPE-EA, respectively). Interestingly, we demonstrated that docosahexaenoylethanolamide (DHEA) is converted by hCOX-2 into the previously unknown metabolites, 13- and 16-hydroxy-DHEA (13- and 16-HDHEA, respectively). These products were also produced by lipopolysaccharide-stimulated RAW267.4 macrophages incubated with DHEA. No oxygenated DHEA metabolites were detected when the selective COX-2 inhibitor, celecoxib, was added to the cells, further underlining the role of COX-2 in the formation of the novel hydroxylated products. This work demonstrates for the first time that DHEA and EPEA are converted by COX-2 into previously unknown hydroxylated metabolites and invites future studies toward the biological effects of these metabolites. en application/pdf https://research.wur.nl/en/publications/novel-cox-2-products-of-n-3-polyunsaturated-fatty-acid-ethanolami 10.1194/jlr.M094235 https://edepot.wur.nl/506704 cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins https://creativecommons.org/licenses/by/4.0/ Wageningen University & Research |
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cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins |
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cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins de Bus, Ian Zuilhof, Han Witkamp, Renger Balvers, Michiel Albada, Bauke Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
description |
Cyclooxygenase 2 (COX-2) plays a key role in the regulation of inflammation by catalyzing the oxygenation of PUFAs to prostaglandins (PGs) and hydroperoxides. Next to this, COX-2 can metabolize neutral lipids, including endocannabinoid-like esters and amides. We developed an LC-HRMS-based human recombinant (h)COX-2 screening assay to examine its ability to also convert n-3 PUFA-derived N-acylethanolamines. Our assay yields known hCOX-2-derived products from established PUFAs and anandamide. Subsequently, we proved that eicosapentaenoylethanolamide (EPEA), the N-acylethanolamine derivative of EPA, is converted into PGE3-ethanolamide (PGE3-EA), and into 11-, 14-, and 18-hydroxyeicosapentaenoyl-EA (11-, 14-, and 18-HEPE-EA, respectively). Interestingly, we demonstrated that docosahexaenoylethanolamide (DHEA) is converted by hCOX-2 into the previously unknown metabolites, 13- and 16-hydroxy-DHEA (13- and 16-HDHEA, respectively). These products were also produced by lipopolysaccharide-stimulated RAW267.4 macrophages incubated with DHEA. No oxygenated DHEA metabolites were detected when the selective COX-2 inhibitor, celecoxib, was added to the cells, further underlining the role of COX-2 in the formation of the novel hydroxylated products. This work demonstrates for the first time that DHEA and EPEA are converted by COX-2 into previously unknown hydroxylated metabolites and invites future studies toward the biological effects of these metabolites. |
format |
Article/Letter to editor |
topic_facet |
cyclooxygenase cyclooxygenase 2 fatty acid amides fatty acid oxidation high-performance liquid chromatography inflammation mass spectrometry prostaglandins |
author |
de Bus, Ian Zuilhof, Han Witkamp, Renger Balvers, Michiel Albada, Bauke |
author_facet |
de Bus, Ian Zuilhof, Han Witkamp, Renger Balvers, Michiel Albada, Bauke |
author_sort |
de Bus, Ian |
title |
Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
title_short |
Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
title_full |
Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
title_fullStr |
Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
title_full_unstemmed |
Novel COX-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in RAW264.7 macrophages |
title_sort |
novel cox-2 products of n-3 polyunsaturated fatty acid-ethanolamine-conjugates identified in raw264.7 macrophages |
url |
https://research.wur.nl/en/publications/novel-cox-2-products-of-n-3-polyunsaturated-fatty-acid-ethanolami |
work_keys_str_mv |
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1822268382697750528 |