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dc.contributor.authorMonsalve-Abaca, Francisco
dc.contributor.authorPyarasani, Radha D.
dc.contributor.authorDelgado-López, Fernando
dc.contributor.authorMoore-Carrasco, Rodrigo
dc.date.accessioned2017-11-15T14:05:46Z
dc.date.available2017-11-15T14:05:46Z
dc.date.issued2013
dc.identifier.urihttp://repositorio.ucm.cl/handle/ucm/1250
dc.description.abstractMetabolic syndrome is estimated to affect more than one in five adults, and its prevalence is growing in the adult and pediatric populations. The most widely recognized metabolic risk factors are atherogenic dyslipidemia, elevated blood pressure, and elevated plasma glucose. Individuals with these characteristics commonly manifest a prothrombotic state and a proinflammatory state as well. Peroxisome proliferator-activated receptors (PPARs) may serve as potential therapeutic targets for treating the metabolic syndrome and its related risk factors. The PPARs are transcriptional factors belonging to the ligand-activated nuclear receptor superfamily. So far, three isoforms of PPARs have been identified, namely, PPAR-𝛼, PPAR-𝛽/𝛿, and PPAR-𝛾. Various endogenous and exogenous ligands of PPARs have been identified. PPAR-𝛼 and PPAR-𝛾 are mainly involved in regulating lipid metabolism, insulin sensitivity, and glucose homeostasis, and their agonists are used in the treatment of hyperlipidemia and T2DM. Whereas PPAR-𝛽/𝛿 function is to regulate lipid metabolism, glucose homeostasis, anti-inflammation, and fatty acid oxidation and its agonists are used in the treatment of metabolic syndrome and cardiovascular diseases. This review mainly focuses on the biological role of PPARs in gene regulation and metabolic diseases, with particular focus on the therapeutic potential of PPAR modulators in the treatment of thrombosis.es_CL
dc.language.isoenes_CL
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
dc.sourceMediators of Inflammation, 2013, 549627es_CL
dc.titlePeroxisome proliferator-cctivated receptor targets for the treatment of metabolic diseaseses_CL
dc.typeArticlees_CL
dc.ucm.facultadFacultad de Medicinaes_CL
dc.ucm.indexacionScopuses_CL
dc.ucm.indexacionIsies_CL
dc.ucm.doidx.doi.org/10.1155/2013/549627es_CL


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