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Licensed Unlicensed Requires Authentication Published by De Gruyter July 12, 2021

Quantitative profiling of inflammatory and pro-resolving lipid mediators in human adolescents and mouse plasma using UHPLC-MS/MS

  • Ivan Hartling ORCID logo , Alessio Cremonesi , Ester Osuna , Phing-How Lou , Eliana Lucchinetti , Michael Zaugg and Martin Hersberger ORCID logo EMAIL logo

Abstract

Objectives

Lipid mediators are bioactive lipids which help regulate inflammation. We aimed to develop an ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method to quantify 58 pro-inflammatory and pro-resolving lipid mediators in plasma, determine preliminary reference ranges for adolescents, and investigate how total parenteral nutrition (TPN) containing omega-3 polyunsaturated fatty acid (n-3 PUFA) or n-6 PUFA based lipid emulsions influence lipid mediator concentrations in plasma.

Methods

Lipid mediators were extracted from plasma using SPE and measured using UHPLC-MS/MS. EDTA plasma was collected from healthy adolescents between 13 and 17 years of age to determine preliminary reference ranges and from mice given intravenous TPN for seven days containing either an n-3 PUFA or n-6 PUFA based lipid emulsion.

Results

We successfully quantified 43 lipid mediators in human plasma with good precision and recovery including several leukotrienes, prostaglandins, resolvins, protectins, maresins, and lipoxins. We found that the addition of methanol to human plasma after blood separation reduces post blood draw increases in 12-hydroxyeicosatetraenoic acid (12-HETE), 12-hydroxyeicosapentaenoic acid (12-HEPE), 12S-hydroxyeicosatrienoic acid (12S-HETrE), 14-hydroxydocosahexaenoic acid (14-HDHA) and thromboxane B2 (TXB2). Compared to the n-6 PUFA based TPN, the n-3 PUFA based TPN increased specialized pro-resolving mediators such as maresin 1 (MaR1), MaR2, protectin D1 (PD1), PDX, and resolvin D5 (RvD5), and decreased inflammatory lipid mediators such as leukotriene B4 (LTB4) and prostaglandin D2 (PGD2).

Conclusions

Our method provides an accurate and sensitive quantification of 58 lipid mediators from plasma samples, which we used to establish a preliminary reference range for lipid mediators in plasma samples of adolescents; and to show that n-3 PUFA, compared to n-6 PUFA rich TPN, leads to a less inflammatory lipid mediator profile in mice.


Corresponding author: Martin Hersberger, Division of Clinical Chemistry and Biochemistry, Children’s Research Center, University Children’s Hospital Zurich, University of Zurich, Steinwiesstr. 75, 8032, Zurich, Switzerland; and Zurich Centre for Integrative Human Physiology, University of Zurich, Zurich, Switzerland, Fax: +41 44 266 71 69, E-mail:

Award Identifier / Grant number: 173088, 177225

  1. Research funding: This study was supported by a project grant (#173088) and a Sinergia grant (#177225) of the Swiss National Science Foundation. The funding organization played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The research related to human use has complied with all the relevant national regulations, institutional policies, and in accordance with the tenets of the Helsinki Declaration, and has been approved by the authors’ Institutional Review Board or equivalent committee (Clinical trial registry number, NCT04158869). The research related to animals’ use has complied with all the relevant national regulations and institutional policies for the care and use of animals (University of Alberta Animal Policy and Welfare Committee, AUP00002007).

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2021-0644).


Received: 2021-02-03
Accepted: 2021-06-29
Published Online: 2021-07-12
Published in Print: 2021-10-26

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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