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Prostaglandins, leukotrienes, and essential fatty acids2026; 209; 102735; doi: 10.1016/j.plefa.2026.102735

Analysis of lipid mediator profiles in the blood of horses with equine asthma using UPLC-MS/MS.

Abstract: Equine asthma (EA) is a chronic inflammatory disease of the lower respiratory tract in horses, which is mainly triggered by dusty hay. EA is becoming increasingly acknowledged as a valuable animal model for studying human asthma. Research on the pathogenesis of EA has primarily focused on the associated cells and cytokines involved. However, the role of inflammation-related lipid mediators (LM) in the development and progression of equine asthma remains elusive. LMs are categorized into pro-inflammatory arachidonic acid (AA)-derived leukotrienes (LTs) and prostaglandins (PGs), as well as inflammation-resolving LMs derived from omega-3 fatty acids, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). In this study, targeted liquid chromatography-tandem mass spectrometry-based metabololipidomics was employed to analyze LM profiles from serum and stimulated whole blood samples collected from 30 healthy horses and from 30 horses with EA. We found that the levels of free fatty acids, as well as their metabolomes, vary substantially among individual horses in serum. In this regard, we observed no significant differences between healthy horses and those with EA, highlighting the complexity of the pathogenesis of respiratory disease in horses. In detail, we detected 12-hydroxyeicosatetraenoic acid (HETE) as the most abundant LM in serum and stimulated whole blood. Furthermore, we found that the levels of LMs decrease with increasing age of the horses. Conclusively, this study presents the comprehensive assessment of LM profiles in serum and stimulated whole blood from horses, which can serve as scientific basis for transferring findings from equine to human asthma.
Publication Date: 2026-03-05 PubMed ID: 41797066DOI: 10.1016/j.plefa.2026.102735Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study analyzed lipid mediators in the blood of horses with equine asthma using advanced mass spectrometry techniques.
  • The research aims to better understand the role of inflammation-related lipids in equine asthma and their relevance as a model for human asthma.

Background and Significance

  • Equine asthma (EA) is a chronic inflammatory disease affecting the lower respiratory tract of horses.
  • EA is primarily triggered by environmental factors such as dusty hay.
  • The disease is increasingly used as an animal model for studying human asthma because of similar pathological features.
  • Previous EA research focused mainly on cellular and cytokine involvement in inflammation.
  • However, the role of lipid mediators (LMs), which regulate inflammation, is less understood in this context.

Lipid Mediators and Their Classification

  • Lipid mediators are bioactive lipids that influence inflammatory processes in the body.
  • They are broadly categorized into:
    • Pro-inflammatory LMs derived from arachidonic acid (AA), including leukotrienes (LTs) and prostaglandins (PGs).
    • Inflammation-resolving LMs derived from omega-3 fatty acids such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA).

Methodology

  • Targeted metabololipidomics was used, employing advanced ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
  • Samples consisted of serum and stimulated whole blood.
  • The study involved 30 healthy horses and 30 horses diagnosed with equine asthma.
  • This approach enabled precise quantification and profiling of various lipid mediators in the blood.

Key Findings

  • There was considerable individual variability in free fatty acid levels and their metabolic profiles among horses.
  • No significant differences in lipid mediator profiles were observed between healthy horses and those with equine asthma.
  • This lack of significant difference highlights the complex nature and multifactorial pathogenesis of equine respiratory disease.
  • The most abundant lipid mediator detected was 12-hydroxyeicosatetraenoic acid (12-HETE) in both serum and stimulated whole blood.
  • Additionally, lipid mediator levels tended to decrease with increasing age of the horses.

Implications and Conclusions

  • This study offers the first comprehensive profiling of lipid mediators in the blood of horses with and without equine asthma.
  • The findings contribute to a better understanding of the inflammatory lipid environment in EA, although direct disease-specific biomarkers were not found.
  • The results underscore the complexity of equine asthma pathogenesis and possible influences such as age and individual variation.
  • The lipid mediator profiles generated could serve as a valuable reference for future comparative studies between equine and human asthma.
  • This research supports the use of EA as a translational model to gain insights into lipid mediator-driven inflammation in human asthma.

Cite This Article

APA
Dörsam K, Nischang V, Büttner K, Fey K, Werz O, Jordan PM. (2026). Analysis of lipid mediator profiles in the blood of horses with equine asthma using UPLC-MS/MS. Prostaglandins Leukot Essent Fatty Acids, 209, 102735. https://doi.org/10.1016/j.plefa.2026.102735

Publication

ISSN: 1532-2823
NlmUniqueID: 8802730
Country: Scotland
Language: English
Volume: 209
Pages: 102735
PII: S0952-3278(26)00013-X

Researcher Affiliations

Dörsam, Kerstin
  • Equine Clinic, Internal Medicine, Faculty of Veterinary Medicine, Justus-Liebig-University, 35392, Giessen, Germany.
Nischang, Vivien
  • Department of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, 07743, Jena, Germany.
Büttner, Kathrin
  • Unit for Biomathematics and Data Processing, Faculty of Veterinary Medicine, Justus-Liebig-University, 35392, Giessen, Germany.
Fey, Kerstin
  • Equine Clinic, Internal Medicine, Faculty of Veterinary Medicine, Justus-Liebig-University, 35392, Giessen, Germany.
Werz, Oliver
  • Department of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, 07743, Jena, Germany; Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, 07743, Jena, Germany.
Jordan, Paul M
  • Department of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, 07743, Jena, Germany; Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, 07743, Jena, Germany. Electronic address: paul.jordan@uni-jena.de.

Conflict of Interest Statement

Declaration of competing interest The authors declare that there is no conflict of interest.

Citations

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