Volume 62, Issue 2
RESEARCH ARTICLE

High Resolution Mass Spectrometric Analysis of Secoiridoids and Metabolites as Biomarkers of Acute Olive Oil Intake—An Approach to Study Interindividual Variability in Humans

Sandra Silva

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal

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Mar Garcia‐Aloy

Biomarkers & Nutrimetabolomic Laboratory, Department of Nutrition, Food Sciences and Gastronomy, Food Technology Reference Net (XaRTA), Nutrition and Food Safety Research Institute (INSA), Faculty of Pharmacy and Food Sciences, University of Barcelona, Barcelona, Spain

CIBER de Fragilidad y Envejecimiento Saludable (CIBERFES), Instituto de Salud Carlos III, Barcelona, Spain

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Maria Eduardo Figueira

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal

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Emilie Combet

Human Nutrition, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK

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William Mullen

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK

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Maria Rosário Bronze

Corresponding Author

E-mail address: mrbronze@ff.ulisboa.pt

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal

Correspondence:

Prof. Maria Rosário Bronze

E‐mail: mrbronze@ff.ulisboa.pt

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First published: 25 October 2017
Citations: 2

Abstract

Scope

Phenolic compounds are minor components of extra virgin olive oil (EVOO). Secoiridoids are the major components contributing to the phenolic content of EVOO. Information is lacking regarding their potential as biomarkers for EVOO intake.

Methods and results

Healthy volunteers (n = 9) ingested 50 mL of EVOO in a single dose containing 322 mg kg−1 total phenolic content (caffeic acid equivalents) and 6 mg 20 g−1 hydroxytyrosol and its derivatives. Plasma is collected before (0 h) and at 0.5, 1, 2, 4, and 6 h after ingestion. Urine samples are collected prior to ingestion (0 h) and at 0–4, 4–8, 8–15, and 15–24 h. Samples are analyzed by UPLC coupled with an Exactive Orbitrap MS. Partial least squares discriminant analysis with orthogonal signal correction is applied to screen for metabolites that allow sample discrimination. Plasma biomarkers and urine biomarkers are selected although individual variability is observed among volunteers. Results are in accordance with in vitro experiments performed (in vitro digestion and hepatic microsomal activity assays).

Conclusions

Plasma (elenolic acid + H2; p‐HPEA‐EA + H2 + glucuronide) and urinary (3,4‐DHPEA‐EA, 3,4‐DHPEA‐EA + H2+glucuronide, methyl 3,4‐DHPEA‐EA + H2+glucuronide) secoiridoid compounds are selected as biomarkers to monitor EVOO intake showing good predictive ability according to multivariate analysis.

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