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dc.contributor.authorTrepiana Arin, Jenifer ORCID
dc.contributor.authorKrisa, Stéphanie
dc.contributor.authorRenouf, Elodie
dc.contributor.authorPortillo Baquedano, María Puy ORCID
dc.date.accessioned2020-10-30T10:50:43Z
dc.date.available2020-10-30T10:50:43Z
dc.date.issued2020-09-30
dc.identifier.citationPharmaceuticals 13(10) : (2020) // Article ID 285es_ES
dc.identifier.issn1424-8247
dc.identifier.urihttp://hdl.handle.net/10810/47522
dc.description.abstractSteatosis is characterized primarily by excessive lipid accumulation in the form of triglycerides in the liver. Although resveratrol shows a low bioavailability, it has significant positive effects on steatosis. The aim of this study was to analyze whether some phase II and microbial resveratrol metabolites (trans-resveratrol-4′-O-glucuronide (R-4G); trans-resveratrol-3-O-glucuronide (R-3G); trans-resveratrol-3-O-sulfate (R-S) and dihydro-resveratrol (DH-R) were effective in reducing hepatocyte fat accumulation. An in vitro model mimicking the hepatocyte situation in fatty liver was developed by incubating mouse AML12 hepatocytes with palmitic acid (PA). For cell treatments, hepatocytes were incubated with 1, 10, or 25 µM resveratrol or its metabolites. Triglycerides and cell viability were assessed using commercial kits. Protein expression of enzymes and transporters involved in triglyceride metabolism were analyzed by western blot. We show for the first time that resveratrol and all the tested metabolites, at 1 µM, partially prevented lipid accumulation induced by the saturated fatty acid PA in AML12 hepatocytes. This effect was mainly due to the inhibition of de novo lipogenesis. This demonstrates that the low bioavailability of resveratrol is not as big a problem as it was thought to be, because resveratrol metabolites contribute to the delipidating effects of the parent compound.es_ES
dc.description.sponsorshipThis research was funded by Ministerio de Economía y Competitividad-Fondo Europeo de Desarrollo Regional, grant number AGL-2015-65719-R; Instituto de Salud Carlos III CIBERobn, grant number CB12/03/30007; University of the Basque Country, grant number GIU 18/173.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/AGL-2015-65719-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectresveratrol metaboliteses_ES
dc.subjecttrans-resveratrol-4′-O-glucuronidees_ES
dc.subjecttrans-resveratrol-3-O-glucuronidees_ES
dc.subjecttrans-resveratrol-3-O-sulfatees_ES
dc.subjectdihydroresveratroles_ES
dc.subjectliver steatosises_ES
dc.subjectAML12 hepatocyteses_ES
dc.titleResveratrol Metabolites Are Able to Reduce Steatosis in Cultured Hepatocyteses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-10-26T14:23:41Z
dc.rights.holder2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1424-8247/13/10/285/htmes_ES
dc.identifier.doi10.3390/ph13100285
dc.departamentoesFarmacia y ciencias de los alimentos
dc.departamentoeuFarmazia eta elikagaien zientziak


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2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).