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dc.contributor.authorAlberdi, Goiuri
dc.contributor.authorRodríguez Rivera, Víctor Manuel
dc.contributor.authorMiranda Gómez, Jonatan ORCID
dc.contributor.authorMacarulla Arenaza, María Teresa ORCID
dc.contributor.authorArias Rueda, Noemí
dc.contributor.authorAndrés Lacueva, Cristina
dc.contributor.authorPortillo Baquedano, María Puy ORCID
dc.date.accessioned2014-02-20T13:31:45Z
dc.date.available2014-02-20T13:31:45Z
dc.date.issued2011-05
dc.identifier.citationNutrition & Metabolism 8 : (2011) // Article n. 29es
dc.identifier.issn1743-7075
dc.identifier.urihttp://hdl.handle.net/10810/11583
dc.description.abstractBackground: A remarkable range of biological functions have been ascribed to resveratrol. Recently, this polyphenol has been shown to have body fat lowering effects. The aim of the present study was to assess some of the potential underlying mechanisms of action which take place in adipose tissue. Methods: Sixteen male Sprague-Dawley rats were randomly divided into two groups: control and treated with 30 mg resveratrol/kg body weight/d. All rats were fed an obesogenic diet and after six weeks of treatment white adipose tissues were dissected. Lipoprotein lipase activity was assessed by fluorimetry, acetyl-CoA carboxylase by radiometry, and malic enzyme, glucose-6P-dehydrogenase and fatty acid synthase by spectrophotometry. Gene expression levels of acetyl-CoA carboxylase, fatty acid synthase, lipoprotein lipase, hormone-sensitive lipase, adipose triglyceride lipase, PPAR-gamma, SREBP-1c and perilipin were assessed by Real time RT-PCR. The amount of resveratrol metabolites in adipose tissue was measured by chromatography. Results: There was no difference in the final body weight of the rats; however, adipose tissues were significantly decreased in the resveratrol-treated group. Resveratrol reduced the activity of lipogenic enzymes, as well as that of heparin-releasable lipoprotein lipase. Moreover, a significant reduction was induced by this polyphenol in hormone-sensitive lipase mRNA levels. No significant changes were observed in other genes. Total amount of resveratrol metabolites in adipose tissue was 2.66 +/- 0.55 nmol/g tissue. Conclusions: It can be proposed that the body fat-lowering effect of resveratrol is mediated, at least in part, by a reduction in fatty acid uptake from circulating triacylglycerols and also in de novo lipogenesis.es
dc.description.sponsorshipThis study was supported by grants from the Ministerio de Ciencia e Innovacion (AGL2008-1005-ALI and partially by the AGL2006-14228-C03-02), Instituto de Salud Carlos III (RETIC PREDIMED) and the Government of Pais Vasco (IT-386-10; CTP09/R5). G. Alberdi is a recipient of a doctoral fellowship from the Ministerio de Ciencia e Innovacion. Resveratrol was a generous gift from Monteloeder (Elche, Alicante, Spain).es
dc.language.isoenges
dc.publisherBioMed Centrales
dc.relationinfo:eu-repo/grantAgreement/MICINN/AGL2008-1005-ALI
dc.relationinfo:eu-repo/grantAgreement/MICINN/AGL2006-14228-C03-02
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectfat mobilizationes
dc.subjectlinoleic acides
dc.subjectbody fates
dc.subjectadipocyteses
dc.subjectmicees
dc.subjectdietes
dc.subjectobesityes
dc.subjectSIRT1es
dc.subjectmodulationes
dc.subjectexpressiones
dc.titleChanges in white adipose tissue metabolism induced by resveratrol in ratses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2011 Alberdi et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es
dc.relation.publisherversionhttp://www.nutritionandmetabolism.com/content/8/1/29es
dc.identifier.doi10.1186/1743-7075-8-29
dc.departamentoesFarmacia y ciencias de los alimentoses_ES
dc.departamentoeuFarmazia eta elikagaien zientziakes_ES
dc.subject.categoriaENDOCRINOLOGY AND METABOLISM
dc.subject.categoriaNUTRITION AND DIETETICS
dc.subject.categoriaMEDICINE


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