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dc.creatorILLANES,JULIO
dc.creatorDABANCENS,ALFREDO
dc.creatorACUÑA,OLGA
dc.creatorFUENZALIDA,MARCELA
dc.creatorGUERRERO,ANIBAL
dc.creatorLOPEZ,CLAUDIA
dc.creatorLEMUS,DAVID
dc.date2002-01-01
dc.date.accessioned2019-05-02T21:21:07Z
dc.date.available2019-05-02T21:21:07Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000300008
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/81433
dc.descriptionIn this study, we showed the effect of the betamethasone, sulindac and quinacrine alone or combined, on the inflammatory angiogenesis promoted by polyurethane sponge on mice. The main finding reported here is that the formation of new blood vessels was strongly inhibited by low concentration of betamethasone, sulindac or quinacrine, whether alone or in combination. It is known that steroidal anti-inflammatory drugs inhibit the enzymes required for the production of prostaglandins through a nuclear glucocorticoid receptor (GR) mediated mechanism. This mechanism may occur in endothelial cells as well. Considering that activity of cyclo-oxigenases 1 and 2 is inhibited by sulindac, and that these enzymes are located in the stromal tissue, we propose that the anti-angiogenic effect of these agents may occur via inhibition of both COX isoforms. On the other hand, quinacrine inhibited PLA2 activity, and we propose here that the anti-angiogenic effect occurs via inhibition of the enzyme PLA2. The potentiated effect of the association of betamethasone, sulindac and quinacrine may have some therapeutic benefit in the control of pathological angiogenesis. Further studies are required to validate these propositions
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dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602002000300008
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.35 n.3-4 2002
dc.subjectangiogenesis
dc.subjectantiangiogenesis
dc.subjectbetamethasone
dc.subjectsulindac
dc.subjectquinacrine
dc.titleEffects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse


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