Oral Bioavailability and Metabolism of Hydroxytyrosol from Food Supplements.

3,4-dihydroxyphenyl-ethanol 3,4-dihydroxyphenylacetic acid bioavailability homovanillic acid hydroxytyrosol hydroxytyrosol glucuronide hydroxytyrosol sulphate oleuropein olive phenolics

Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
09 Jan 2023
Historique:
received: 21 11 2022
revised: 02 01 2023
accepted: 05 01 2023
entrez: 21 1 2023
pubmed: 22 1 2023
medline: 25 1 2023
Statut: epublish

Résumé

Table olives and olive oils are the main dietary sources of hydroxytyrosol (HT), a natural antioxidant compound that has emerged as a potential aid in protection against cardiovascular risk. Bioavailability studies with olive oils showed that HT is bioavailable from its free form and from conjugated forms such as oleuropein and its aglycone. Still, its low dietary intake, poor bioavailability, and high inter-individual variability after absorption through the gastrointestinal tract hamper its full benefits. In a randomized, controlled, blinded, cross-over study, we investigated the impact of HT metabolism and bioavailability by comparing two olive-derived watery supplements containing different doses of HT (30.58 and 61.48 mg of HT/dosage). Additionally, HT-fortified olive oil was used in the control group. To this aim, plasma and urine samples were evaluated in 12 healthy volunteers following the intake of a single dose of the supplements or fortified olive oil. Blood and urine samples were collected at baseline and at 0.5, 1, 1.5, 2, 4, and 12 h after intake. HT and its metabolites were analyzed using UHPLC-DAD-MS/MS. Pharmacokinetic results showed that dietary HT administered through the food supplements is bioavailable and bioavailability increases with the administered dose. After intake, homovanillic acid, HT-3-

Identifiants

pubmed: 36678196
pii: nu15020325
doi: 10.3390/nu15020325
pmc: PMC9866489
pii:
doi:

Substances chimiques

Olive Oil 0
3,4-dihydroxyphenylethanol 10597-60-1
Phenylethyl Alcohol ML9LGA7468
Antioxidants 0
Plant Oils 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Cecilia Bender (C)

Institut Kurz GmbH, Stöckheimer Weg 1, 50829 Köln, Germany.
Istituto Kurz Italia S.R.L., Via Golfo dei Poeti 1/A, 43126 Parma, Italy.

Sarah Strassmann (S)

Institut Kurz GmbH, Stöckheimer Weg 1, 50829 Köln, Germany.

Christian Golz (C)

Institut Kurz GmbH, Stöckheimer Weg 1, 50829 Köln, Germany.
Institut für Physik, Humboldt, Universität zu Berlin, Newtonstrasse 15, 12489 Berlin, Germany.

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Classifications MeSH