Flax phenolic compounds as inhibitors of lipid oxidation: Elucidation of their mechanisms of action.


Journal

Food chemistry
ISSN: 1873-7072
Titre abrégé: Food Chem
Pays: England
ID NLM: 7702639

Informations de publication

Date de publication:
15 Feb 2019
Historique:
received: 12 02 2018
revised: 24 08 2018
accepted: 28 08 2018
entrez: 31 10 2018
pubmed: 31 10 2018
medline: 19 12 2018
Statut: ppublish

Résumé

Polyunsaturated fatty acids are particularly sensitive to the damages due to reactive oxygen species and lipid oxidation has been reported to be involved in the degradation of food as well as in the early stages of several diseases. Our objective was to study the mechanisms of action of flax (Linum usitatissimum) phenolic compounds to prevent membrane lipid oxidation. To do so, several biophysical techniques (oxidative stress, surface tension, fluorescence spectroscopy and HPLC) were used to investigate the ability of the compounds to prevent lipid oxidation and to interact with membranes. We evidenced a relationship between the structure and the antioxidant efficiency as aglycone compounds were significantly more efficient (p < 0.05) than glucoside compounds. In addition, our results revealed that aglycone lignans spontaneously penetrated the membrane contrary to aglycone hydroxycinnamic acids. To conclude, the comparison of the antioxidant efficiencies revealed that membrane inserted compounds better inhibited lipid oxidation than non-inserted compounds.

Identifiants

pubmed: 30372990
pii: S0308-8146(18)31539-5
doi: 10.1016/j.foodchem.2018.08.126
pii:
doi:

Substances chimiques

Antioxidants 0
Fatty Acids, Unsaturated 0
Lignans 0
Liposomes 0
Phenols 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

651-658

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Larissa Socrier (L)

Sorbonne Universités, Université de technologie de Compiègne, Laboratoire de Génie Enzymatique et Cellulaire, FRE 3580 CNRS, Centre de recherches de Royallieu, CS 60319, 60203 Compiègne cedex, France.

Anthony Quéro (A)

Université Picardie Jules Verne, EA3900 BioPI - UFR de Pharmacie, 1 rue des Louvels, 80037 Amiens cedex, France.

Margaux Verdu (M)

Sorbonne Universités, Université de technologie de Compiègne, Laboratoire de Génie Enzymatique et Cellulaire, FRE 3580 CNRS, Centre de recherches de Royallieu, CS 60319, 60203 Compiègne cedex, France.

Yiming Song (Y)

Sorbonne Universités, Université de technologie de Compiègne, Laboratoire de Génie Enzymatique et Cellulaire, FRE 3580 CNRS, Centre de recherches de Royallieu, CS 60319, 60203 Compiègne cedex, France.

Roland Molinié (R)

Université Picardie Jules Verne, EA3900 BioPI - UFR de Pharmacie, 1 rue des Louvels, 80037 Amiens cedex, France.

David Mathiron (D)

Université Picardie Jules Verne, Plateforme analytique, Rue Dallery - Passage du sourire d'Avril, 80039 Amiens cedex, France.

Serge Pilard (S)

Université Picardie Jules Verne, Plateforme analytique, Rue Dallery - Passage du sourire d'Avril, 80039 Amiens cedex, France.

François Mesnard (F)

Université Picardie Jules Verne, EA3900 BioPI - UFR de Pharmacie, 1 rue des Louvels, 80037 Amiens cedex, France.

Sandrine Morandat (S)

Sorbonne Universités, Université de technologie de Compiègne, Laboratoire de Génie Enzymatique et Cellulaire, FRE 3580 CNRS, Centre de recherches de Royallieu, CS 60319, 60203 Compiègne cedex, France. Electronic address: sandrine.morandat@utc.fr.

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Classifications MeSH