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Title:
Quantitative profiling of oxylipins through comprehensive LC-MS/MS analysis: application in cardiac surgery | Analytical and Bioanalytical Chemistry
Description:
Oxylipins, including eicosanoids, affect a broad range of biological processes, such as the initiation and resolution of inflammation. These compounds, also referred to as lipid mediators, are (non-) enzymatically generated by oxidation of polyunsaturated fatty acids such as arachidonic acid (AA). A plethora of lipid mediators exist which makes the development of generic analytical methods challenging. Here we developed a robust and sensitive targeted analysis platform for oxylipins and applied it in a biological setting, using high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) operated in dynamic multiple reaction monitoring (dMRM). Besides the well-described AA metabolites, oxylipins derived from linoleic acid, dihomo-γ-linolenic acid, α-linolenic acid, eicosapentaenoic acid and docosahexaenoic acid were included. Our comprehensive platform allows the quantitative evaluation of approximately 100 oxylipins down to low nanomolar levels. Applicability of the analytical platform was demonstrated by analyzing plasma samples of patients undergoing cardiac surgery. Altered levels of some of the oxylipins, especially in certain monohydroxy fatty acids such as 12-HETE and 12-HEPE, were observed in samples collected before and 24 h after cardiac surgery. These findings indicate that this generic oxylipin profiling platform can be applied broadly to study these highly bioactive compounds in relation to human disease.
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Keywords {🔍}
google, scholar, article, cas, oxylipins, acid, surgery, human, levels, compounds, metabolites, plasma, acids, fig, derived, prostaglandins, lipid, mass, oxylipin, analysis, lox, cardiac, hete, liquid, spectrometry, eicosanoids, detection, patients, table, platform, min, fatty, high, samples, detected, matrix, van, inflammation, arachidonic, mrm, performed, method, level, analytical, lcmsms, observed, related, pufas, time, netherlands,
Topics {✒️}
comprehensive lc-ms/ms analysis liquid chromatography-mass spectrometric numerous lc-ms/ms methods 6-trans-ltb4/6-trans-12-epi ltb4 improved lc-ms/ms method generic lc-ms/ms platform gas chromatography–mass spectrometry tandem mass spectrometry lc-ms/ms chromatogram lc-ms/ms analysis residual double-bond number poly-unsaturated fatty acids lc-ms/ms method triple quadrupole system hplc-ms/ms approach circadian rhythm-dependent cycling high-throughput protein quantitation related hydroxy-fatty acids dihomo-γ-linolenic acid cyp epoxygenase-dependent metabolism van der greef user-defined time segments full size image ischemic-reperfused rat hearts epa-derived hydroxypentaenoic acids 14-dihydro-15-keto-pgf1α/1a netherlands metabolomics centre anti-inflammatory lipid mediators electronic supplementary material hplc-ms/ms ischemic/reperfused cardiac tissue gas chromatography coupled article download pdf 6-keto-pgf1α change rapidly substantial inter-patient variation la-derived hydroxyoctadecadienoic acids 100 nm 1-cyclohexyluriedo-3-dodecanoic acid electronic supplementary materials liquid chromatography privacy choices/manage cookies lox-dependent products include multiple reaction monitoring mass hunter quan monohydroxy fatty acids 19-hydroxy-pgf2α/20-hydroxy-pgf2α bioanalytical chemistry aims ltb4/12-epi ltb4 aa-derived hydroxyeicosatetraenoic acids john van duynhoven myocardial ischemia/reperfusion injury
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headline:Quantitative profiling of oxylipins through comprehensive LC-MS/MS analysis: application in cardiac surgery
description:Oxylipins, including eicosanoids, affect a broad range of biological processes, such as the initiation and resolution of inflammation. These compounds, also referred to as lipid mediators, are (non-) enzymatically generated by oxidation of polyunsaturated fatty acids such as arachidonic acid (AA). A plethora of lipid mediators exist which makes the development of generic analytical methods challenging. Here we developed a robust and sensitive targeted analysis platform for oxylipins and applied it in a biological setting, using high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) operated in dynamic multiple reaction monitoring (dMRM). Besides the well-described AA metabolites, oxylipins derived from linoleic acid, dihomo-γ-linolenic acid, α-linolenic acid, eicosapentaenoic acid and docosahexaenoic acid were included. Our comprehensive platform allows the quantitative evaluation of approximately 100 oxylipins down to low nanomolar levels. Applicability of the analytical platform was demonstrated by analyzing plasma samples of patients undergoing cardiac surgery. Altered levels of some of the oxylipins, especially in certain monohydroxy fatty acids such as 12-HETE and 12-HEPE, were observed in samples collected before and 24 h after cardiac surgery. These findings indicate that this generic oxylipin profiling platform can be applied broadly to study these highly bioactive compounds in relation to human disease.
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headline:Quantitative profiling of oxylipins through comprehensive LC-MS/MS analysis: application in cardiac surgery
description:Oxylipins, including eicosanoids, affect a broad range of biological processes, such as the initiation and resolution of inflammation. These compounds, also referred to as lipid mediators, are (non-) enzymatically generated by oxidation of polyunsaturated fatty acids such as arachidonic acid (AA). A plethora of lipid mediators exist which makes the development of generic analytical methods challenging. Here we developed a robust and sensitive targeted analysis platform for oxylipins and applied it in a biological setting, using high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) operated in dynamic multiple reaction monitoring (dMRM). Besides the well-described AA metabolites, oxylipins derived from linoleic acid, dihomo-γ-linolenic acid, α-linolenic acid, eicosapentaenoic acid and docosahexaenoic acid were included. Our comprehensive platform allows the quantitative evaluation of approximately 100 oxylipins down to low nanomolar levels. Applicability of the analytical platform was demonstrated by analyzing plasma samples of patients undergoing cardiac surgery. Altered levels of some of the oxylipins, especially in certain monohydroxy fatty acids such as 12-HETE and 12-HEPE, were observed in samples collected before and 24 h after cardiac surgery. These findings indicate that this generic oxylipin profiling platform can be applied broadly to study these highly bioactive compounds in relation to human disease.
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name:Adrie Dane
affiliation:
name:Leiden Amsterdam Centre for Drug Research, Leiden University
address:
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Ruud Berger
affiliation:
name:University Medical Centre Utrecht
address:
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Arjan Brenkman
affiliation:
name:University Medical Centre Utrecht
address:
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Thomas Hankemeier
affiliation:
name:Leiden Amsterdam Centre for Drug Research, Leiden University
address:
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:John van Duynhoven
affiliation:
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Unilever Research and Development, Olivier van Noortlaan 120
address:
name:Unilever Research and Development, Olivier van Noortlaan 120, Vlaardingen, The Netherlands
type:PostalAddress
type:Organization
name:Wageningen University
address:
name:Laboratory of Biophysics, Wageningen University, Wageningen, The Netherlands
type:PostalAddress
type:Organization
name:Eric Kalkhoven
affiliation:
name:University Medical Centre Utrecht
address:
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:John W. Newman
affiliation:
name:430 West Health Sciences
address:
name:USDA-ARS Western Human Nutrition Research Center, 430 West Health Sciences, Davis, USA
type:PostalAddress
type:Organization
name:University of California, 430 West Health Sciences
address:
name:Department of Nutrition, University of California, 430 West Health Sciences, Davis, USA
type:PostalAddress
type:Organization
name:Rob J. Vreeken
affiliation:
name:Leiden Amsterdam Centre for Drug Research, Leiden University
address:
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Netherlands Metabolomics Centre
address:
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
type:PostalAddress
type:Organization
name:Leiden Amsterdam Centre for Drug Research, Leiden University
address:
name:Department of Analytical BioSciences, Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
type:PostalAddress
type:Organization
email:[email protected]
PostalAddress:
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, The Netherlands
name:Department of General Surgery, Leiden University Medical Center, Leiden, The Netherlands
name:USDA-ARS Western Human Nutrition Research Center, 430 West Health Sciences, Davis, USA
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Unilever Research and Development, Olivier van Noortlaan 120, Vlaardingen, The Netherlands
name:Laboratory of Biophysics, Wageningen University, Wageningen, The Netherlands
name:Department of Metabolic and Endocrine Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:USDA-ARS Western Human Nutrition Research Center, 430 West Health Sciences, Davis, USA
name:Department of Nutrition, University of California, 430 West Health Sciences, Davis, USA
name:Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
name:Netherlands Metabolomics Centre, Leiden, The Netherlands
name:Department of Analytical BioSciences, Leiden Amsterdam Centre for Drug Research, Leiden University, Leiden, The Netherlands
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