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Peanut skin polyphenols inhibit toxicity induced by advanced glycation end-products in RAW264.7 macrophages

dc.contributor.authorFernandes, Annayara Celestina Ferreira
dc.contributor.authorVieira, Natália Carolina [UNESP]
dc.contributor.authorSantana, Ádina Lima de
dc.contributor.authorGandra, Renata Luana de Pádua
dc.contributor.authorRubia, Camila
dc.contributor.authorCastro-Gamboa, Ian [UNESP]
dc.contributor.authorMacedo, Juliana Alves
dc.contributor.authorMacedo, Gabriela Alves
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Nebraska-Lincoln
dc.date.accessioned2020-12-12T01:35:03Z
dc.date.available2020-12-12T01:35:03Z
dc.date.issued2020-11-01
dc.description.abstractThis is the first work to use a polyphenolic fraction derived from peanut skin to attenuate the toxicity induced by advanced glycation-end products (AGEs) in RAW264.7 macrophages. The RAW264.7 cells were stimulated by AGEs using the bovine serum albumin-fructose (BSA-FRU), bovine serum albumin-methylglyoxal (BSA-MGO) and arginine-methylglyoxal (ARG-MGO) models. The AGEs increased considerably the levels of reactive oxygen species and the gene expression of proinflammatory cytokines interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), and nitric oxide. Twenty-eight polyphenols, including catechin, phenolic acids, and resveratrol were annotated in peanut skin extract (PSE) with the use of ultra-performance liquid chromatography coupled to quadrupole time of flight mass spectrometry (UPLC-QTOF/MSE) and to the UNIFI Scientific Information System. The administration of PSE at 100 and 150 μg/mL significantly inhibited oxidative stress, by suppressing the production of reactive oxygen species up to 70% and reducing the production of nitric oxide, IL-6 and TNF-α up to 1.7-, 10- and 107-fold, respectively.en
dc.description.affiliationSchool of Food Engineering Food and Nutrition Department University of Campinas (UNICAMP)
dc.description.affiliationCenter for Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Institute of Chemistry (ICAr) Sao Paulo State University (UNESP)
dc.description.affiliation264 Food Innovation Center University of Nebraska-Lincoln, 1901 N 21st Street
dc.description.affiliationUnespCenter for Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Institute of Chemistry (ICAr) Sao Paulo State University (UNESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdCNPq: 140884/2016-5
dc.description.sponsorshipIdFAPESP: 2018/24868-3
dc.identifierhttp://dx.doi.org/10.1016/j.fct.2020.111619
dc.identifier.citationFood and Chemical Toxicology, v. 145.
dc.identifier.doi10.1016/j.fct.2020.111619
dc.identifier.issn1873-6351
dc.identifier.issn0278-6915
dc.identifier.scopus2-s2.0-85089482649
dc.identifier.urihttp://hdl.handle.net/11449/199260
dc.language.isoeng
dc.relation.ispartofFood and Chemical Toxicology
dc.sourceScopus
dc.subjectAdvanced glycation end-products
dc.subjectInflammation
dc.subjectMethylglyoxal
dc.subjectPeanut skin
dc.subjectPhenolic compounds
dc.subjectRAW264.7 macrophages
dc.titlePeanut skin polyphenols inhibit toxicity induced by advanced glycation end-products in RAW264.7 macrophagesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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