Show simple item record

Authordc.contributor.authorCosta de Camargo, Adriano
Authordc.contributor.authorÁlvarez Larraín, Alina Concepción
Authordc.contributor.authorArias Santé, María Fernanda
Authordc.contributor.authorOyarzún, Juan Estebán
Authordc.contributor.authorAndia, Marcelo E.
Authordc.contributor.authorUribe, Sergio
Authordc.contributor.authorNúñez Pizarro, Paula
Authordc.contributor.authorBustos, Simón M.
Authordc.contributor.authorSchwember, Andrés R.
Authordc.contributor.authorShahidi, Fereidoon
Authordc.contributor.authorBridi, Raquel
Admission datedc.date.accessioned2022-07-25T16:10:32Z
Available datedc.date.available2022-07-25T16:10:32Z
Publication datedc.date.issued2022
Cita de ítemdc.identifier.citationAntioxidants 2022, 11, 1139es_ES
Identifierdc.identifier.other10.3390/antiox11061139
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/186924
Abstractdc.description.abstractChickpeas are rich sources of bioactive compounds such as phenolic acids, flavonoids, and isoflavonoids. However, the contribution of insoluble-bound phenolics to their antioxidant properties remains unclear. Four varieties of chickpeas were evaluated for the presence of soluble (free and esterified) and insoluble-bound phenolics as well as their antiradical activity, reducing power and inhibition of peroxyl-induced cytotoxicity in human HuH-7 cells. In general, the insoluble-bound fraction showed a higher total phenolic content. Phenolic acids, flavonoids, and isoflavonoids were identified and quantified by UPLC-MS/MS. Taxifolin was identified for the first time in chickpeas. However, m-hydroxybenzoic acid, taxifolin, and biochanin A were the main phenolics found. Biochanin A was mostly found in the free fraction, while m-hydroxybenzoic acid was present mainly in the insoluble-bound form. The insoluble-bound fraction made a significant contribution to the reducing power and antiradical activity towards peroxyl radical. Furthermore, all extracts decreased the oxidative damage of human HuH-7 cells induced by peroxyl radicals, thus indicating their hepatoprotective potential. This study demonstrates that the antioxidant properties and bioactive potential of insoluble-bound phenolics of chickpeas should not be neglected.es_ES
Patrocinadordc.description.sponsorshipANID/CONICYT, FONDECYT postdoctorado 3180432 University of Chile (Vicerrectoria de Investigacion y Desarrollo (VID) de la Universidad de Chile) UI-005/20 ANID-Millennium Science Initiative Program ICN2021_004 Natural Sciences and Engineering Research Council of Canada (NSERC) Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 1220922es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceAntioxidantses_ES
Keywordsdc.subjectCicer arietinum Les_ES
Keywordsdc.subjectPhenolic acidses_ES
Keywordsdc.subjectFlavonoidses_ES
Keywordsdc.subjectReducing poweres_ES
Keywordsdc.subjectAntiradical activityes_ES
Keywordsdc.subjectHepatoprotectiones_ES
Títulodc.titleSoluble free, esterified and insoluble-bound phenolic antioxidants from chickpeas prevent cytotoxicity in human hepatoma HuH-7 cells induced by peroxyl radicalses_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States