A sensitive LC-MS/MS method for the quantification of regioisomers of epoxyeicosatrienoic and dihydroxyeicosatrienoic acids in human plasma during endothelial stimulation
Autor: | Fabien Lamoureux, Tony Pereira, Robinson Joannides, Pascal Cardinael, Patricia Compagnon, Michele Iacob, Najla El-Gharbi Hamza, Thomas Duflot, Jeremy Bellien, Christian Thuillez, Clothilde Roche |
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Přispěvatelé: | Sciences et Méthodes Séparatives (SMS), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU), Propre |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Epoxide hydrolase 2 [SDV]Life Sciences [q-bio] Vasodilation Stimulation Arachidonic Acids 01 natural sciences Biochemistry Analytical Chemistry 03 medical and health sciences Limit of Detection Tandem Mass Spectrometry [CHIM.ANAL]Chemical Sciences/Analytical chemistry Lc ms ms Structural isomer Humans ComputingMilieux_MISCELLANEOUS Chromatography Chemistry 010401 analytical chemistry Lipid signaling 0104 chemical sciences 030104 developmental biology Human plasma Case-Control Studies Hypertension cardiovascular system lipids (amino acids peptides and proteins) Endothelium Vascular Saponification Chromatography Liquid |
Zdroj: | Analytical and Bioanalytical Chemistry Analytical and Bioanalytical Chemistry, Springer Verlag, 2016, 409 (7), pp.1845-1855. ⟨10.1007/s00216-016-0129-1⟩ |
ISSN: | 1618-2650 1618-2642 |
DOI: | 10.1007/s00216-016-0129-1 |
Popis: | Epoxyeicosatrienoic acids (EETs) are vasodilating lipid mediators metabolized into dihydroxyeicosatrienoic acids (DHETs) by soluble epoxide hydrolase. We aimed to develop a LC-MS/MS method to quantify EETs and DHETs in human plasma and monitored their levels during vascular endothelial stimulation. Plasma samples, collected from 14 healthy and five hypertensive subjects at baseline and during radial artery endothelium-dependent flow-mediated dilatation, were spiked with internal standards. Lipids were then extracted by a modified Bligh and Dyer method and saponified to release bound EETs and DHETs. Samples were purified by a second liquid-liquid extraction and analyzed by LC-MS/MS. The assay allowed identification of (±)8(9)-epoxy-5Z,11Z,14Z-eicosatrienoic acid (8,9-EET); (±)11(12)-epoxy-5Z,8Z,14Z-eicosatrienoic acid (11,12-EET); (±)14(15)-epoxy-5Z,8Z,11Z-eicosatrienoic acid (14,15-EET); (±)8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid (8,9-DHET); (±)11,12-dihydroxy-5Z,8Z,14Z-eicosatrienoic acid (11,12-DHET); and (±)14,15-dihydroxy-5Z,8Z,11Z-eicosatrienoic acid (14,15-DHET). (±)5(6)-epoxy-5Z,11Z,14Z-eicosatrienoic acid (5,6-EET) was virtually undetectable due to its chemical instability. The limits of quantification were 0.25 ng/mL for DHETs and 0.5 ng/mL for EETs. Intra- and inter-assay variations ranged from 1.6 to 13.2%. Heating induced a similar increase in 8,9-EET, 11,12-EET, and 14,15-EET levels and in corresponding DHET levels in healthy but not in hypertensive subjects. We validated a sensitive LC-MS/MS method for measuring simultaneously plasma EET and DHET regioisomers in human plasma and showed its interest for assessing endothelial function. |
Databáze: | OpenAIRE |
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