2024 Technical Program
Lipid Oxidation and Quality
Health and Nutrition
Analytical
Magdalena Osowiecka
PhD Student
Institute of Physiological Chemistry
Wien, Wien, Austria
Yifan Bao, MSc
PhD
Institute of Physiological Chemistry
Wien, Wien, Austria
Matthias Strauss
PhD Student
Institute of Physiological Chemistry, Austria
Christiane Ott
Dr.
DIfE German Institute of Human Nutrition Potsdam-Rehbruecke, Germany
Richard Bleyer
Bachelor
Institute of Physiological Chemistry, Austria
Daniela Krivda
Master Student
Institute of Physiological Chemistry, Austria
Yury Lebedov
Dr.
The Maulide Group, Austria
Sergio Armentia Armentia Matheu
PhD Student
The Maulide Group, Austria
Nuno Maulide
Univ.-Prof. Dr.
The Maulide Group, Austria
Tilman Grune
Univ. Prof. Dr.
Institute of Physiological Chemistry, Austria
Marc Pignitter, PhD
Dr, Assoc. Professor
University of Vienna
Wien, Wien, Austria
Dietary epoxides, which are widely recognized as abundant products of lipid oxidation, are raising concerns regarding their impact on gastrointestinal health. To address this concern, we conducted a study using mice fed a high-fat diet supplemented with naturally occurring epoxidized triacylglycerols (ETAGs) at food representative amounts (4 µg, 20 µg, and 100 µg/day) to investigate their influence on inflammation. Our analysis involved gene expression assessments related to inflammation (TLR4, NF-κB p65, COX-2) using qPCR, along with targeted oxylipin analysis in jejunum tissues using LC-MS/MS.
In the proximal jejunum, supplementation with 100 µg ETAGs/day significantly increased the relative gene expression of NF-κB p65 and COX-2 to 3.00 ± 0.34 and 2.10 ± 0.21 compared to the control (1.0), respectively. Even at 4 µg ETAGs/day, there was a twofold increase in NF-κB p65 expression (2.21 ± 0.11). In the later stages of jejunal digestion, the 20 µg ETAGs/day supplementation led to an almost fivefold increase in TLR4 expression (4.67 ± 0.41) and a more than sixfold increase in COX-2 expression (6.36 ± 0.50) compared to the control.
Profiles of pro-inflammatory oxylipins in distal jejunal tissues showed a significant up to threefold increase in PGE2 and PGD1 compared to the control when mice were fed 4 µg and 100 µg ETAGs/day, respectively. Moreover, the LOX and COX metabolites, HETE, HODE, and HDHA, were notably elevated in the distal jejunum of epoxide-supplemented mice. In the group receiving 4 µg ETAGs/day, 9-HODE increased fourfold, and HETE increased to 30 ng/mg tissue compared to 10 ng/mg in the control. In contrast, soluble epoxide hydrolase activity was substantially reduced in the distal jejunum when mice were supplemented with 100 µg ETAGs/day.
Our results underscore the pro-inflammatory effects of dietary epoxides in the jejunum, emphasizing the importance of considering dietary epoxides in consumer recommendations and developing industry standards.