Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0100-879X2006001100009 http://repositorio.unifesp.br/handle/11600/3334 |
Resumo: | Experimental models of sepsis-induced pulmonary alterations are important for the study of pathogenesis and for potential intervention therapies. The objective of the present study was to characterize lung dysfunction (low PaO2 and high PaCO2, and increased cellular infiltration, protein extravasation, and malondialdehyde (MDA) production assessed in bronchoalveolar lavage) in a sepsis model consisting of intraperitoneal (ip) injection of Escherichia coli and the protective effects of pentoxifylline (PTX). Male Wistar rats (weighing between 270 and 350 g) were injected ip with 10(7) or 10(9) CFU/100 g body weight or saline and samples were collected 2, 6, 12, and 24 h later (N = 5 each group). PaO2, PaCO2 and pH were measured in blood, and cellular influx, protein extravasation and MDA concentration were measured in bronchoalveolar lavage. In a second set of experiments either PTX or saline was administered 1 h prior to E. coli ip injection (N = 5 each group) and the animals were observed for 6 h. Injection of 10(7) or 10(9) CFU/100 g body weight of E. coli induced acidosis, hypoxemia, and hypercapnia. An increased (P < 0.05) cell influx was observed in bronchoalveolar lavage, with a predominance of neutrophils. Total protein and MDA concentrations were also higher (P < 0.05) in the septic groups compared to control. A higher tumor necrosis factor-alpha (P < 0.05) concentration was also found in these animals. Changes in all parameters were more pronounced with the higher bacterial inoculum. PTX administered prior to sepsis reduced (P < 0.05) most functional alterations. These data show that an E. coli ip inoculum is a good model for the induction of lung dysfunction in sepsis, and suitable for studies of therapeutic interventions. |
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Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury modelAcute lung injurySepsisInflammatory mediatorsPentoxifyllineNeutrophilsExperimental models of sepsis-induced pulmonary alterations are important for the study of pathogenesis and for potential intervention therapies. The objective of the present study was to characterize lung dysfunction (low PaO2 and high PaCO2, and increased cellular infiltration, protein extravasation, and malondialdehyde (MDA) production assessed in bronchoalveolar lavage) in a sepsis model consisting of intraperitoneal (ip) injection of Escherichia coli and the protective effects of pentoxifylline (PTX). Male Wistar rats (weighing between 270 and 350 g) were injected ip with 10(7) or 10(9) CFU/100 g body weight or saline and samples were collected 2, 6, 12, and 24 h later (N = 5 each group). PaO2, PaCO2 and pH were measured in blood, and cellular influx, protein extravasation and MDA concentration were measured in bronchoalveolar lavage. In a second set of experiments either PTX or saline was administered 1 h prior to E. coli ip injection (N = 5 each group) and the animals were observed for 6 h. Injection of 10(7) or 10(9) CFU/100 g body weight of E. coli induced acidosis, hypoxemia, and hypercapnia. An increased (P < 0.05) cell influx was observed in bronchoalveolar lavage, with a predominance of neutrophils. Total protein and MDA concentrations were also higher (P < 0.05) in the septic groups compared to control. A higher tumor necrosis factor-alpha (P < 0.05) concentration was also found in these animals. Changes in all parameters were more pronounced with the higher bacterial inoculum. PTX administered prior to sepsis reduced (P < 0.05) most functional alterations. These data show that an E. coli ip inoculum is a good model for the induction of lung dysfunction in sepsis, and suitable for studies of therapeutic interventions.Universidade Federal de São Paulo (UNIFESP) Divisão de Moléstias InfecciosasUniversidade Federal de São Paulo (UNIFESP) Laboratório de Cirurgia ExperimentalUniversidade Federal de São Paulo (UNIFESP) Laboratório de Mediadores InflamatóriosUniversidade Federal de São Paulo (UNIFESP) Laboratório de GeriatriaUNIFESP, Divisão de Moléstias InfecciosasUNIFESP, Laboratório de Cirurgia ExperimentalUNIFESP, Laboratório de Mediadores InflamatóriosUNIFESP, Laboratório de GeriatriaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Oliveira-Júnior, Itamar Souza [UNIFESP]Brunialti, Milena Karina Coló [UNIFESP]Koh, Ivan Hong Jun [UNIFESP]Junqueira, Virginia Berlanga Campos [UNIFESP]Salomão, Reinaldo [UNIFESP]2015-06-14T13:36:31Z2015-06-14T13:36:31Z2006-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1455-1463application/pdfhttp://dx.doi.org/10.1590/S0100-879X2006001100009Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 11, p. 1455-1463, 2006.10.1590/S0100-879X2006001100009S0100-879X2006001100009.pdf0100-879XS0100-879X2006001100009http://repositorio.unifesp.br/handle/11600/3334WOS:000242377200009engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T23:08:27Zoai:repositorio.unifesp.br/:11600/3334Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T23:08:27Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
title |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
spellingShingle |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model Oliveira-Júnior, Itamar Souza [UNIFESP] Acute lung injury Sepsis Inflammatory mediators Pentoxifylline Neutrophils |
title_short |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
title_full |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
title_fullStr |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
title_full_unstemmed |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
title_sort |
Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model |
author |
Oliveira-Júnior, Itamar Souza [UNIFESP] |
author_facet |
Oliveira-Júnior, Itamar Souza [UNIFESP] Brunialti, Milena Karina Coló [UNIFESP] Koh, Ivan Hong Jun [UNIFESP] Junqueira, Virginia Berlanga Campos [UNIFESP] Salomão, Reinaldo [UNIFESP] |
author_role |
author |
author2 |
Brunialti, Milena Karina Coló [UNIFESP] Koh, Ivan Hong Jun [UNIFESP] Junqueira, Virginia Berlanga Campos [UNIFESP] Salomão, Reinaldo [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Oliveira-Júnior, Itamar Souza [UNIFESP] Brunialti, Milena Karina Coló [UNIFESP] Koh, Ivan Hong Jun [UNIFESP] Junqueira, Virginia Berlanga Campos [UNIFESP] Salomão, Reinaldo [UNIFESP] |
dc.subject.por.fl_str_mv |
Acute lung injury Sepsis Inflammatory mediators Pentoxifylline Neutrophils |
topic |
Acute lung injury Sepsis Inflammatory mediators Pentoxifylline Neutrophils |
description |
Experimental models of sepsis-induced pulmonary alterations are important for the study of pathogenesis and for potential intervention therapies. The objective of the present study was to characterize lung dysfunction (low PaO2 and high PaCO2, and increased cellular infiltration, protein extravasation, and malondialdehyde (MDA) production assessed in bronchoalveolar lavage) in a sepsis model consisting of intraperitoneal (ip) injection of Escherichia coli and the protective effects of pentoxifylline (PTX). Male Wistar rats (weighing between 270 and 350 g) were injected ip with 10(7) or 10(9) CFU/100 g body weight or saline and samples were collected 2, 6, 12, and 24 h later (N = 5 each group). PaO2, PaCO2 and pH were measured in blood, and cellular influx, protein extravasation and MDA concentration were measured in bronchoalveolar lavage. In a second set of experiments either PTX or saline was administered 1 h prior to E. coli ip injection (N = 5 each group) and the animals were observed for 6 h. Injection of 10(7) or 10(9) CFU/100 g body weight of E. coli induced acidosis, hypoxemia, and hypercapnia. An increased (P < 0.05) cell influx was observed in bronchoalveolar lavage, with a predominance of neutrophils. Total protein and MDA concentrations were also higher (P < 0.05) in the septic groups compared to control. A higher tumor necrosis factor-alpha (P < 0.05) concentration was also found in these animals. Changes in all parameters were more pronounced with the higher bacterial inoculum. PTX administered prior to sepsis reduced (P < 0.05) most functional alterations. These data show that an E. coli ip inoculum is a good model for the induction of lung dysfunction in sepsis, and suitable for studies of therapeutic interventions. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-11-01 2015-06-14T13:36:31Z 2015-06-14T13:36:31Z |
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/10.1590/S0100-879X2006001100009 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 11, p. 1455-1463, 2006. 10.1590/S0100-879X2006001100009 S0100-879X2006001100009.pdf 0100-879X S0100-879X2006001100009 http://repositorio.unifesp.br/handle/11600/3334 WOS:000242377200009 |
url |
http://dx.doi.org/10.1590/S0100-879X2006001100009 http://repositorio.unifesp.br/handle/11600/3334 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 39, n. 11, p. 1455-1463, 2006. 10.1590/S0100-879X2006001100009 S0100-879X2006001100009.pdf 0100-879X S0100-879X2006001100009 WOS:000242377200009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1455-1463 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
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 |
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1814268366168260608 |