Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/51543
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dc.contributor.authorGalán, M.-
dc.contributor.authorMiguel, Marta-
dc.contributor.authorRodríguez, Cristina-
dc.contributor.authorGarcía-Redondo, Ana B.-
dc.contributor.authorRodríguez-Calvo, R.-
dc.contributor.authorAlonso, M. J.-
dc.contributor.authorMartínez-González, José-
dc.contributor.authorSalaices, M.-
dc.contributor.authorBeltrán, A. E.-
dc.date.accessioned2012-06-14T09:50:49Z-
dc.date.available2012-06-14T09:50:49Z-
dc.date.issued2011-
dc.identifierdoi: 10.1097/HJH.0b013e328342b271-
dc.identifierissn: 0263-6352-
dc.identifiere-issn: 1473-5598-
dc.identifier.citationJournal of Hypertension 29(3): 529-536 (2011)-
dc.identifier.urihttp://hdl.handle.net/10261/51543-
dc.description.abstract[Aims]: To assess whether angiotensin II (Ang II) modulates key enzymes of the cyclooxygenase (COX)-2/prostanoid pathway, including prostaglandin E synthase-1 (mPGES-1) and prostacyclin synthase (PGIS) in rat aortic adventitial fibroblasts in the presence or absence of an inflammatory stimulus [interleukin (IL)-1β]. [Methods and Results]: Fibroblasts stimulated with IL-1β (10 ng/ml, 24 h) and/or Ang II (0.1 μmol/l, 24 h) were used. IL-1β up-regulated COX-2 and mPGES-1 (protein and mRNA) and increased PGI2 and PGE2 release, without altering PGIS protein expression. Ang II did modify neither COX-2 and mPGES-1 expression nor prostanoid levels, but it induced PGIS expression. Interestingly, Ang II further enhanced IL-1β-induced COX-2 expression and PGI2 release and concomitantly reduced IL-1β-induced mPGES-1 expression. The AT1 receptor antagonist losartan prevented the effects of Ang II on IL-1β-induced COX-2 or mPGES-1 expression. IL-1β activated p38 mitogen-activated protein kinase (MAPK) and extracellular signal-regulated kinase (ERK)1/2 pathways, and coincubation with Ang II resulted in a higher and more sustained phosphorylation of both MAPK. Inhibition of either p38 MAPK (SB203580) or ERK1/2 (PD98059) reduced COX-2 and mPGES-1 expression in cells treated with IL-1β or the combination of IL-1β and Ang II. Ang II did not modify COX-2 transcriptional activity but increased COX-2 mRNA stability in IL-1β-treated cells; by contrast, it increased PGIS mRNA levels through a transcriptional mechanism. [Conclusion]: Ang II differentially modulates key enzymes involved in prostanoid biosynthesis thereby altering the balance between PGI2/PGE2 in vascular cells exposed to inflammatory stimuli. © 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins.-
dc.language.isoeng-
dc.publisherLippincott Williams & Wilkins-
dc.rightsclosedAccess-
dc.titleAngiotensin II differentially modulates cyclooxygenase-2, microsomal prostaglandin E2 synthase-1 and prostaglandin I2 synthase expression in adventitial fibroblasts exposed to inflammatory stimuli-
dc.typeartículo-
dc.identifier.doi10.1097/HJH.0b013e328342b271-
dc.date.updated2012-06-14T09:50:49Z-
dc.description.versionPeer Reviewed-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeartículo-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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