Effect of pentoxifylline on lung inflammation and gas exchange in a sepsis-induced acute lung injury model

Detalhes bibliográficos
Autor(a) principal: Oliveira-Júnior, Itamar Souza [UNIFESP]
Data de Publicação: 2006
Outros Autores: Brunialti, Milena Karina Coló [UNIFESP], Koh, Ivan Hong Jun [UNIFESP], Junqueira, Virginia Berlanga Campos [UNIFESP], Salomão, Reinaldo [UNIFESP]
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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spelling 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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