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Título

Preventive Oral Treatment with Resveratrol Pro-prodrugs Drastically Reduce Colon Inflammation in Rodents

AutorLarrosa, Mar CSIC ORCID; Tomé-Carneiro, Joao CSIC ORCID; Yáñez-Gascón, María J. CSIC ORCID; Alcántara, David CSIC; Selma, María Victoria CSIC ORCID ; Beltrán Riquelme, David; García-Conesa, María Teresa CSIC ORCID ; Urbán, Cristina CSIC; Lucas, Ricardo CSIC; Tomás Barberán, Francisco CSIC ORCID ; Morales, Juan C.; Espín de Gea, Juan Carlos CSIC ORCID
Palabras claveInflamatory bowel diseases (IBDs)
Polyphenol
Anti-inflammatory
Colon
Dextran suflate sodium (DSS)
Resveratrol
Fecha de publicación24-sep-2010
EditorAmerican Chemical Society
CitaciónJournal of Medicinal of Chemistry 53(20): 7365-7376 (2010)
ResumenThere is no pharmaceutical or definitive surgical cure for inflammatory bowel diseases (IBDs). The naturally occurring polyphenol resveratrol exerts anti-inflammatory properties. However, its rapid metabolism diminishes its effectiveness in the colon. The design of prodrugs to targeting active molecules to the colon provides an opportunity for therapy of IBDs. Herein we explore the efficacy of different resveratrol prodrugs and pro-prodrugs to ameliorate colon inflammation in the murine dextran sulfate sodium (DSS) model. Mice fed with a very low dose (equivalent to 10 mg for a 70 kg-person) of either resveratrol-3-O-(6′-O-butanoyl)-β-d-glucopyranoside (6) or resveratrol-3-O-(6′-O-octanoyl)-β-d-glucopyranoside (7) did not develop colitis symptoms and improved 6-fold the disease activity index (DAI) compared to resveratrol. Our results indicate that these pro-prodrugs exerted a dual effect: (1) they prevented the rapid metabolism of resveratrol and delivered higher quantities of resveratrol to the colon and (2) they reduced mucosal barrier imbalance and prevented diarrhea, which consequently facilitated the action of the delivered resveratrol in the colon mucosa.
Descripción12 páginas, 7 figuras, 2 esquemas.
Versión del editorhttp://dx.doi.org/10.1021/jm1007006
URIhttp://hdl.handle.net/10261/37441
DOI10.1021/jm1007006
ISSN0022-2623
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