Response activity of alveolar macrophages in pulmonary dysfunction caused by Leptospira infection

Bibliographic Details
Main Author: Marinho, Márcia [UNESP]
Publication Date: 2008
Other Authors: Oliveira-Júnior, I. S., Perri, Silvia Helena Venturoli [UNESP], Peiró, Juliana Regina [UNESP], Pavanelli, T. F., Salomão, R.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1590/S1678-91992008000100005
http://hdl.handle.net/11449/26915
Summary: 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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spelling 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.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)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 ReproductionUNIFESP Department of Parasitological and Infectious DiseasesSão Paulo State University FOA Microbiology LaboratoryUNESP FOA Department of Clinics, Surgery and Animal ReproductionUniversidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)Universidade Estadual Paulista (Unesp)Universidade Federal de São Paulo (UNIFESP)Marinho, Márcia [UNESP]Oliveira-Júnior, I. S.Perri, Silvia Helena Venturoli [UNESP]Peiró, Juliana Regina [UNESP]Pavanelli, T. F.Salomão, R.2014-05-20T15:08:33Z2014-05-20T15:08:33Z2008-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article58-70application/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, 2008.1678-9199http://hdl.handle.net/11449/2691510.1590/S1678-91992008000100005S1678-91992008000100005WOS:000254511600005S1678-91992008000100005.pdfSciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxins Including Tropical Diseases1.7820,573info:eu-repo/semantics/openAccess2025-06-07T05:20:39Zoai:repositorio.unesp.br:11449/26915Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-06-07T05:20:39Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)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 [UNESP]
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 [UNESP]
author_facet Marinho, Márcia [UNESP]
Oliveira-Júnior, I. S.
Perri, Silvia Helena Venturoli [UNESP]
Peiró, Juliana Regina [UNESP]
Pavanelli, T. F.
Salomão, R.
author_role author
author2 Oliveira-Júnior, I. S.
Perri, Silvia Helena Venturoli [UNESP]
Peiró, Juliana Regina [UNESP]
Pavanelli, T. F.
Salomão, R.
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 [UNESP]
Oliveira-Júnior, I. S.
Perri, Silvia Helena Venturoli [UNESP]
Peiró, Juliana Regina [UNESP]
Pavanelli, T. F.
Salomão, R.
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
2014-05-20T15:08:33Z
2014-05-20T15:08:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv
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.
1678-9199
http://hdl.handle.net/11449/26915
10.1590/S1678-91992008000100005
S1678-91992008000100005
WOS:000254511600005
S1678-91992008000100005.pdf
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.
1678-9199
10.1590/S1678-91992008000100005
S1678-91992008000100005
WOS:000254511600005
S1678-91992008000100005.pdf
url http://dx.doi.org/10.1590/S1678-91992008000100005
http://hdl.handle.net/11449/26915
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Venomous Animals and Toxins Including Tropical Diseases
1.782
0,573
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 Universidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)
dc.source.none.fl_str_mv SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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