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dc.contributor.authorPalacios-Ramirez, Roberto
dc.contributor.authorLima-Posada, Ixchel
dc.contributor.authorBonnard, Benjamin
dc.contributor.authorGenty, Marie
dc.contributor.authorFernandez-Celis, Amaya
dc.contributor.authorHartleib-Geschwindner, Judith
dc.contributor.authorFoufelle, Fabienne
dc.contributor.authorLopez-Andres, Natalia
dc.contributor.authorBamberg, Krister
dc.contributor.authorJaisser, Frederic
dc.date.accessioned2024-02-07T15:12:41Z
dc.date.available2024-02-07T15:12:41Z
dc.date.issued2022-04-07
dc.identifier.citationFront Physiol. 2022 Apr 7:13:859812.es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/65927
dc.descriptionProducción Científicaes
dc.description.abstractObesity and/or metabolic diseases are frequently associated with chronic kidney disease and several factors associated with obesity may contribute to proteinuria and extracellular matrix production. Mineralocorticoid receptor antagonists have proven their clinical efficacy in diabetic kidney disease with preclinical data suggesting that they may also be efficient in non-diabetic chronic kidney disease associated to metabolic diseases. In the present study we developed a novel mouse model combining severe nephron reduction and High Fat Diet challenge that led to chronic kidney disease with metabolic alterations. We showed that the Mineralocorticoid Receptor antagonist canrenoate improved metabolic function, reduced albuminuria and prevented the synergistic effect of high fat diet on renal fibrosis and inflammation in chronic kidney disease mice.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationCKD-chronic kidney disease; fibrosis; inflammation; kidney; mineralocorticod receptorses
dc.titleMineralocorticoid Receptor Antagonism Prevents the Synergistic Effect of Metabolic Challenge and Chronic Kidney Disease on Renal Fibrosis and Inflammation in Micees
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.3389/fphys.2022.859812es
dc.relation.publisherversionhttps://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2022.859812/fulles
dc.identifier.publicationtitleFrontiers in Physiologyes
dc.identifier.publicationvolume13es
dc.peerreviewedSIes
dc.identifier.essn1664-042Xes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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