Identification of Peptides Potentially Responsible for In Vivo Hypolipidemic Activity of a Hydrolysate from Olive Seeds
Authors
Marina Alegre, María LuisaIdentifiers
Permanent link (URI): http://hdl.handle.net/10017/44569DOI: 10.1021/acs.jafc.0c01280
ISSN: 0021-8561
Date
2020-03-18Embargo end date
2021-03-18Affiliation
Universidad de Alcalá. Departamento de Química Analítica, Química Física e Ingeniería QuímicaBibliographic citation
Journal of Agricultural and Food Chemistry, 2020, v. 68, n. 14, p. 4237-4244
Keywords
hypolipidemic activity
peptides
in vivo assay
olive seed
mass spectrometry
Project
AGL2016-79010-R (Ministerio de Economía y Competitividad de España) Comunidad Autónoma de Madrid y FEDER (S2018 / BAA-4393, AVANSECAL II-CM).
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
© ACS
Access rights
info:eu-repo/semantics/openAccess
Abstract
Previous studies demonstrated that peptides produced by the hydrolysis of olive seed proteins using Alcalase enzyme showed in vitro multifunctional lipid-lowering capability. This work presents a deeper insight into the hypolipidemic effect of olive seed peptides. The capability of olive seed peptides to inhibit endogenous cholesterol biosynthesis through the inhibition of HMGCoA reductase enzyme was evaluated observing a 38 ± 7% of inhibition. Two in vivo assays using different peptides concentrations (200 and 400 mg/kg/day) were designed to evaluate the hypolipidemic effect of olive seed peptides in male and female mice. A low concentration of hydrolysate reduced total cholesterol in male mice in a 20% after 11 weeks compared to the mice feeding with hypercholesterolemic diet. A higher hydrolysate concentration showed a greater reduction in total cholesterol (25%). The analysis of the olive seed hydrolysate by reverse phase high-performance liquid chromatography mass spectrometry (RP-HPLC-MS) enabled the identification of peptides that could be responsible for this hypolipidemic effect.
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