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pubmed-article:15037537pubmed:abstractTextClinical trials have demonstrated that agents that inhibit the angiotensin II pathway confer benefit beyond the reduction of blood pressure alone. However, the molecular mechanism underlying this effect has yet to be investigated. Recently, we have demonstrated enhanced expression of inducible cyclooxygenase (COX) and prostaglandin (PG)E2-dependent synthase (COX-2/mPGES-1) in human symptomatic plaques and provided evidence that it is associated with metalloproteinase (MMP)-induced plaque rupture. Thus, the aim of this study was to characterize the effect of the angiotensin II type 1 (AT1) receptor antagonist irbesartan on the inflammatory infiltration and expression of COX-2/mPGES-1 and MMPs in human carotid plaques.lld:pubmed
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pubmed-article:15037537pubmed:articleTitleBlockade of the angiotensin II type 1 receptor stabilizes atherosclerotic plaques in humans by inhibiting prostaglandin E2-dependent matrix metalloproteinase activity.lld:pubmed
pubmed-article:15037537pubmed:affiliationG. d'Annunzio University of Chieti and the G. d'Annunzio University Foundation, Chieti, Italy.lld:pubmed
pubmed-article:15037537pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15037537pubmed:publicationTypeClinical Triallld:pubmed
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