Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse

In 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 beta...

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Auteurs principaux: ILLANES,JULIO, DABANCENS,ALFREDO, ACUÑA,OLGA, FUENZALIDA,MARCELA, GUERRERO,ANIBAL, LOPEZ,CLAUDIA, LEMUS,DAVID
Langue:English
Publié: Sociedad de Biología de Chile 2002
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Accès en ligne:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000300008
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spelling oai:scielo:S0716-976020020003000082003-11-26Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouseILLANES,JULIODABANCENS,ALFREDOACUÑA,OLGAFUENZALIDA,MARCELAGUERRERO,ANIBALLOPEZ,CLAUDIALEMUS,DAVID angiogenesis antiangiogenesis betamethasone sulindac quinacrine In 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 propositionsinfo:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.35 n.3-4 20022002-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000300008en10.4067/S0716-97602002000300008
institution Scielo Chile
collection Scielo Chile
language English
topic angiogenesis
antiangiogenesis
betamethasone
sulindac
quinacrine
spellingShingle angiogenesis
antiangiogenesis
betamethasone
sulindac
quinacrine
ILLANES,JULIO
DABANCENS,ALFREDO
ACUÑA,OLGA
FUENZALIDA,MARCELA
GUERRERO,ANIBAL
LOPEZ,CLAUDIA
LEMUS,DAVID
Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
description In 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
author ILLANES,JULIO
DABANCENS,ALFREDO
ACUÑA,OLGA
FUENZALIDA,MARCELA
GUERRERO,ANIBAL
LOPEZ,CLAUDIA
LEMUS,DAVID
author_facet ILLANES,JULIO
DABANCENS,ALFREDO
ACUÑA,OLGA
FUENZALIDA,MARCELA
GUERRERO,ANIBAL
LOPEZ,CLAUDIA
LEMUS,DAVID
author_sort ILLANES,JULIO
title Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
title_short Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
title_full Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
title_fullStr Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
title_full_unstemmed Effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
title_sort effects of betamethasone, sulindac and quinacrine drugs on the inflammatory neoangiogenesis response induced by polyurethane sponge implanted in mouse
publisher Sociedad de Biología de Chile
publishDate 2002
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000300008
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