MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR
Autor(a) principal: | |
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Data de Publicação: | 1994 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1155/S0962935194000177 http://repositorio.unifesp.br/handle/11600/25390 |
Resumo: | The role of endogenously synthesized PAF and prostaglandins on the infection of mouse macrophages by Leishmania (L.) amazonensis was investigated, as well as the possible correlation between the effects of these inflammatory mediators with nitric oxide production. It was found that pretreatment of macrophages with 10(-5) M of the PAF antagonists, BN-52021 or WEB-2086, increased macrophage infection by 17 and 59%, respectively. the cyclooxygenase inhibitor, Indomethacin (10 mu g/ml), induced a significant inhibition which was reversed by addition of PGE, (10(-5) M) to the culture medium. These results suggested that the infection of macrophages by Leishmania Is Inhibited by PAF and enhanced by prostaglandins and that these mediators are produced by macrophages during this infection. This was confirmed by addition of these mediators to the culture medium before infection; PAF (10(-6), 10(-9) and 10(-12) M) reduced significantly the infection whereas PGE, (10(-5) M) induced a marked enhancement. This effect of exogenous PAF on macrophage Infection was reversed by the two PAF antagonists used in this study as well as by the inhibitor of nitric oxide synthesis, L-arginine methyl ester (100 mM). Taken together the data suggest that endogenous production of PAF and PGE, exert opposing effects on Leishmania-macrophage interaction and that nitric oxide may be involved in the augmented destruction of parasites induced by PAF. |
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Repositório Institucional da UNIFESP |
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MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTORLEISHMANIASISLEISHMANIA (L) AMAZONENSISMACROPHAGE INFECTIONPAFPROSTAGLANDINSThe role of endogenously synthesized PAF and prostaglandins on the infection of mouse macrophages by Leishmania (L.) amazonensis was investigated, as well as the possible correlation between the effects of these inflammatory mediators with nitric oxide production. It was found that pretreatment of macrophages with 10(-5) M of the PAF antagonists, BN-52021 or WEB-2086, increased macrophage infection by 17 and 59%, respectively. the cyclooxygenase inhibitor, Indomethacin (10 mu g/ml), induced a significant inhibition which was reversed by addition of PGE, (10(-5) M) to the culture medium. These results suggested that the infection of macrophages by Leishmania Is Inhibited by PAF and enhanced by prostaglandins and that these mediators are produced by macrophages during this infection. This was confirmed by addition of these mediators to the culture medium before infection; PAF (10(-6), 10(-9) and 10(-12) M) reduced significantly the infection whereas PGE, (10(-5) M) induced a marked enhancement. This effect of exogenous PAF on macrophage Infection was reversed by the two PAF antagonists used in this study as well as by the inhibitor of nitric oxide synthesis, L-arginine methyl ester (100 mM). Taken together the data suggest that endogenous production of PAF and PGE, exert opposing effects on Leishmania-macrophage interaction and that nitric oxide may be involved in the augmented destruction of parasites induced by PAF.UNIV São Paulo,INST CIENCIAS BIOMED,DEPT IMMUNOL,BR-05508900 São Paulo,BRAZILUNIV ESTADUAL MARINGA,DEPT BIOCHEM,PARANA,BRAZILESCOLA PAULISTA MED,DEPT MICROBIOL IMMUNOL & PARASITOL,São Paulo,BRAZILESCOLA PAULISTA MED,DEPT MICROBIOL IMMUNOL & PARASITOL,São Paulo,BRAZILWeb of ScienceRapid Science PublishersUniversidade de São Paulo (USP)Universidade Estadual de Maringá (UEM)Universidade Federal de São Paulo (UNIFESP)Lonardoni, MVCBarbieri, C. L.Russo, Marisa [UNIFESP]Jancar, S.2016-01-24T11:40:17Z2016-01-24T11:40:17Z1994-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion137-141application/pdfhttp://dx.doi.org/10.1155/S0962935194000177Mediators of Inflammation. London: Rapid Science Publishers, v. 3, n. 2, p. 137-141, 1994.10.1155/S0962935194000177WOSA1994NJ21900006.pdf0962-9351http://repositorio.unifesp.br/handle/11600/25390WOS:A1994NJ21900006engMediators of Inflammationinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-30T18:04:23Zoai:repositorio.unifesp.br/:11600/25390Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-30T18:04:23Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
title |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
spellingShingle |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR Lonardoni, MVC LEISHMANIASIS LEISHMANIA (L) AMAZONENSIS MACROPHAGE INFECTION PAF PROSTAGLANDINS |
title_short |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
title_full |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
title_fullStr |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
title_full_unstemmed |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
title_sort |
MODULATION of LEISHMANIA (L) AMAZONENSIS GROWTH in CULTURED MOUSE MACROPHAGES BY PROSTAGLANDINS and PLATELET-ACTIVATING-FACTOR |
author |
Lonardoni, MVC |
author_facet |
Lonardoni, MVC Barbieri, C. L. Russo, Marisa [UNIFESP] Jancar, S. |
author_role |
author |
author2 |
Barbieri, C. L. Russo, Marisa [UNIFESP] Jancar, S. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual de Maringá (UEM) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Lonardoni, MVC Barbieri, C. L. Russo, Marisa [UNIFESP] Jancar, S. |
dc.subject.por.fl_str_mv |
LEISHMANIASIS LEISHMANIA (L) AMAZONENSIS MACROPHAGE INFECTION PAF PROSTAGLANDINS |
topic |
LEISHMANIASIS LEISHMANIA (L) AMAZONENSIS MACROPHAGE INFECTION PAF PROSTAGLANDINS |
description |
The role of endogenously synthesized PAF and prostaglandins on the infection of mouse macrophages by Leishmania (L.) amazonensis was investigated, as well as the possible correlation between the effects of these inflammatory mediators with nitric oxide production. It was found that pretreatment of macrophages with 10(-5) M of the PAF antagonists, BN-52021 or WEB-2086, increased macrophage infection by 17 and 59%, respectively. the cyclooxygenase inhibitor, Indomethacin (10 mu g/ml), induced a significant inhibition which was reversed by addition of PGE, (10(-5) M) to the culture medium. These results suggested that the infection of macrophages by Leishmania Is Inhibited by PAF and enhanced by prostaglandins and that these mediators are produced by macrophages during this infection. This was confirmed by addition of these mediators to the culture medium before infection; PAF (10(-6), 10(-9) and 10(-12) M) reduced significantly the infection whereas PGE, (10(-5) M) induced a marked enhancement. This effect of exogenous PAF on macrophage Infection was reversed by the two PAF antagonists used in this study as well as by the inhibitor of nitric oxide synthesis, L-arginine methyl ester (100 mM). Taken together the data suggest that endogenous production of PAF and PGE, exert opposing effects on Leishmania-macrophage interaction and that nitric oxide may be involved in the augmented destruction of parasites induced by PAF. |
publishDate |
1994 |
dc.date.none.fl_str_mv |
1994-04-01 2016-01-24T11:40:17Z 2016-01-24T11:40:17Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1155/S0962935194000177 Mediators of Inflammation. London: Rapid Science Publishers, v. 3, n. 2, p. 137-141, 1994. 10.1155/S0962935194000177 WOSA1994NJ21900006.pdf 0962-9351 http://repositorio.unifesp.br/handle/11600/25390 WOS:A1994NJ21900006 |
url |
http://dx.doi.org/10.1155/S0962935194000177 http://repositorio.unifesp.br/handle/11600/25390 |
identifier_str_mv |
Mediators of Inflammation. London: Rapid Science Publishers, v. 3, n. 2, p. 137-141, 1994. 10.1155/S0962935194000177 WOSA1994NJ21900006.pdf 0962-9351 WOS:A1994NJ21900006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Mediators of Inflammation |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
137-141 application/pdf |
dc.publisher.none.fl_str_mv |
Rapid Science Publishers |
publisher.none.fl_str_mv |
Rapid Science Publishers |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268414837915648 |