Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S1678-91992008000100005 http://repositorio.unifesp.br/handle/11600/4148 |
Resumo: | Leptopspirosis is a syndrome with different clinical manifestations including the most severe and often fatal forms of pulmonary disease of unknown etiology. Pulmonary injury during the inflammatory process has been associated with the excessive number of alveolar macrophages (AMs) and polymorphonuclear leukocytes stimulated in the lungs and with the production of reactive oxygen and nitrogen intermediates and other inflammatory mediators. The aim of the present work was to evaluate the cellular immune response of AMs or inflammatory cells of hamsters during leptospirosis. The activity of AMs was determined by measuring nitric oxide (NO) and protein production as well as inflammatory cell infiltration in bronchoalveolar lavage (BAL) fluid. Pulmonary activity during infection was monitored by measuring pH, pressure of oxygen (PaO2), and pressure of carbon dioxide (PaCO2) in blood samples. Cellular immune response and its role in the genesis of leptospirosis have been incriminated as the main causes of tissue and pulmonary injuries, which consequently lead to the pulmonary dysfunction in severe cases of leptospirosis. The present results show a low production of NO in both supernatant of alveolar macrophage culture and BAL. In the latter, protein production was high and constant, especially during acute infection. Total and differential cell count values were 2.5X10(6) on day 4; 7.3X10(6) on day 21; and 2.3X10(6) on day 28 after infection, with lymphocytes (84.04%) predominating over neutrophils (11.88%) and monocytes (4.07%). Arterial blood gas analysis showed pulmonary compromising along with the infectious process, as observed in parameter values (mean±SD) evidenced in the infected versus control group: PaO2 (60.47mmHg±8.7 vs. 90.09mmHg±9.18), PaCO2 (57.01mmHg±7.87 vs. 47.39mmHg±4.5) and pH (7.39±0.03 vs. 6.8±1.3). Results indicated that Leptospira infection in hamsters is a good experimental model to study leptospirosis. However, some of the immune parameters showed variations which might be associated with the animal species. |
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Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infectionalveolar macrophagesbronchoalveolar lavagegasometrypulmonary dysfunctionhamstersLeptospiraLeptopspirosis is a syndrome with different clinical manifestations including the most severe and often fatal forms of pulmonary disease of unknown etiology. Pulmonary injury during the inflammatory process has been associated with the excessive number of alveolar macrophages (AMs) and polymorphonuclear leukocytes stimulated in the lungs and with the production of reactive oxygen and nitrogen intermediates and other inflammatory mediators. The aim of the present work was to evaluate the cellular immune response of AMs or inflammatory cells of hamsters during leptospirosis. The activity of AMs was determined by measuring nitric oxide (NO) and protein production as well as inflammatory cell infiltration in bronchoalveolar lavage (BAL) fluid. Pulmonary activity during infection was monitored by measuring pH, pressure of oxygen (PaO2), and pressure of carbon dioxide (PaCO2) in blood samples. Cellular immune response and its role in the genesis of leptospirosis have been incriminated as the main causes of tissue and pulmonary injuries, which consequently lead to the pulmonary dysfunction in severe cases of leptospirosis. The present results show a low production of NO in both supernatant of alveolar macrophage culture and BAL. In the latter, protein production was high and constant, especially during acute infection. Total and differential cell count values were 2.5X10(6) on day 4; 7.3X10(6) on day 21; and 2.3X10(6) on day 28 after infection, with lymphocytes (84.04%) predominating over neutrophils (11.88%) and monocytes (4.07%). Arterial blood gas analysis showed pulmonary compromising along with the infectious process, as observed in parameter values (mean±SD) evidenced in the infected versus control group: PaO2 (60.47mmHg±8.7 vs. 90.09mmHg±9.18), PaCO2 (57.01mmHg±7.87 vs. 47.39mmHg±4.5) and pH (7.39±0.03 vs. 6.8±1.3). Results indicated that Leptospira infection in hamsters is a good experimental model to study leptospirosis. However, some of the immune parameters showed variations which might be associated with the animal species.São Paulo State University FOA Microbiology LaboratoryFederal University of São Paulo Division of Geriatric and Gerontology Inflammatory Mediators LaboratoryUNESP FOA Department of Clinics, Surgery and Animal ReproductionUniversidade Federal de São Paulo (UNIFESP) Department of Parasitological and Infectious DiseasesUNIFESP, Division of Geriatric and Gerontology Inflammatory Mediators LaboratoryUNIFESP, Department of Parasitological and Infectious DiseasesSciELOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESPUniversidade Estadual Paulista (UNESP)Universidade Federal de São Paulo (UNIFESP)Marinho, MárciaOliveira-Júnior, Itamar Souza [UNIFESP]Perri, Sílvia Helena VenturoliPeiró, Juliana ReginaPavanelli, Tais Francisco [UNIFESP]Salomão, Reinaldo [UNIFESP]2015-06-14T13:38:17Z2015-06-14T13:38:17Z2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion58-70application/pdfhttp://dx.doi.org/10.1590/S1678-91992008000100005Journal of Venomous Animals and Toxins including Tropical Diseases. Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 14, n. 1, p. 58-70, 2008.10.1590/S1678-91992008000100005S1678-91992008000100005.pdf1678-9199S1678-91992008000100005http://repositorio.unifesp.br/handle/11600/4148WOS:000254511600005engJournal of Venomous Animals and Toxins including Tropical Diseasesinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-30T02:51:44Zoai:repositorio.unifesp.br/:11600/4148Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-30T02:51:44Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
title |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
spellingShingle |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection Marinho, Márcia alveolar macrophages bronchoalveolar lavage gasometry pulmonary dysfunction hamsters Leptospira |
title_short |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
title_full |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
title_fullStr |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
title_full_unstemmed |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
title_sort |
Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection |
author |
Marinho, Márcia |
author_facet |
Marinho, Márcia Oliveira-Júnior, Itamar Souza [UNIFESP] Perri, Sílvia Helena Venturoli Peiró, Juliana Regina Pavanelli, Tais Francisco [UNIFESP] Salomão, Reinaldo [UNIFESP] |
author_role |
author |
author2 |
Oliveira-Júnior, Itamar Souza [UNIFESP] Perri, Sílvia Helena Venturoli Peiró, Juliana Regina Pavanelli, Tais Francisco [UNIFESP] Salomão, Reinaldo [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Marinho, Márcia Oliveira-Júnior, Itamar Souza [UNIFESP] Perri, Sílvia Helena Venturoli Peiró, Juliana Regina Pavanelli, Tais Francisco [UNIFESP] Salomão, Reinaldo [UNIFESP] |
dc.subject.por.fl_str_mv |
alveolar macrophages bronchoalveolar lavage gasometry pulmonary dysfunction hamsters Leptospira |
topic |
alveolar macrophages bronchoalveolar lavage gasometry pulmonary dysfunction hamsters Leptospira |
description |
Leptopspirosis is a syndrome with different clinical manifestations including the most severe and often fatal forms of pulmonary disease of unknown etiology. Pulmonary injury during the inflammatory process has been associated with the excessive number of alveolar macrophages (AMs) and polymorphonuclear leukocytes stimulated in the lungs and with the production of reactive oxygen and nitrogen intermediates and other inflammatory mediators. The aim of the present work was to evaluate the cellular immune response of AMs or inflammatory cells of hamsters during leptospirosis. The activity of AMs was determined by measuring nitric oxide (NO) and protein production as well as inflammatory cell infiltration in bronchoalveolar lavage (BAL) fluid. Pulmonary activity during infection was monitored by measuring pH, pressure of oxygen (PaO2), and pressure of carbon dioxide (PaCO2) in blood samples. Cellular immune response and its role in the genesis of leptospirosis have been incriminated as the main causes of tissue and pulmonary injuries, which consequently lead to the pulmonary dysfunction in severe cases of leptospirosis. The present results show a low production of NO in both supernatant of alveolar macrophage culture and BAL. In the latter, protein production was high and constant, especially during acute infection. Total and differential cell count values were 2.5X10(6) on day 4; 7.3X10(6) on day 21; and 2.3X10(6) on day 28 after infection, with lymphocytes (84.04%) predominating over neutrophils (11.88%) and monocytes (4.07%). Arterial blood gas analysis showed pulmonary compromising along with the infectious process, as observed in parameter values (mean±SD) evidenced in the infected versus control group: PaO2 (60.47mmHg±8.7 vs. 90.09mmHg±9.18), PaCO2 (57.01mmHg±7.87 vs. 47.39mmHg±4.5) and pH (7.39±0.03 vs. 6.8±1.3). Results indicated that Leptospira infection in hamsters is a good experimental model to study leptospirosis. However, some of the immune parameters showed variations which might be associated with the animal species. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01 2015-06-14T13:38:17Z 2015-06-14T13:38:17Z |
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/10.1590/S1678-91992008000100005 Journal of Venomous Animals and Toxins including Tropical Diseases. Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 14, n. 1, p. 58-70, 2008. 10.1590/S1678-91992008000100005 S1678-91992008000100005.pdf 1678-9199 S1678-91992008000100005 http://repositorio.unifesp.br/handle/11600/4148 WOS:000254511600005 |
url |
http://dx.doi.org/10.1590/S1678-91992008000100005 http://repositorio.unifesp.br/handle/11600/4148 |
identifier_str_mv |
Journal of Venomous Animals and Toxins including Tropical Diseases. Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP, v. 14, n. 1, p. 58-70, 2008. 10.1590/S1678-91992008000100005 S1678-91992008000100005.pdf 1678-9199 S1678-91992008000100005 WOS:000254511600005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Venomous Animals and Toxins including Tropical Diseases |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
58-70 application/pdf |
dc.publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP |
publisher.none.fl_str_mv |
Centro de Estudos de Venenos e Animais Peçonhentos - CEVAP, Universidade Estadual Paulista - UNESP |
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_ |
1814268289750138880 |