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Acute lung injury induced by the intravenous administration of cigarette smoke extract

OBJECTIVE: To investigate the acute effects of intravenous administration of cigarette smoke extract (CSE) on histological, inflammatory, and respiratory function parameters in rats, as well as to compare this potential acute lung injury (ALI) model with that with the use of oleic acid (OA). METHODS...

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Autores principales: Menezes, Luciana Gomes, Uzuelli, Juliana Alves, Tefé-Silva, Cristiane, Ramos, Simone Gusmão, dos Santos, José Eduardo Tanus, Martinez, José Antônio Baddini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Pneumologia e Tisiologia 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075806/
https://www.ncbi.nlm.nih.gov/pubmed/23503484
http://dx.doi.org/10.1590/S1806-37132013000100006
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author Menezes, Luciana Gomes
Uzuelli, Juliana Alves
Tefé-Silva, Cristiane
Ramos, Simone Gusmão
dos Santos, José Eduardo Tanus
Martinez, José Antônio Baddini
author_facet Menezes, Luciana Gomes
Uzuelli, Juliana Alves
Tefé-Silva, Cristiane
Ramos, Simone Gusmão
dos Santos, José Eduardo Tanus
Martinez, José Antônio Baddini
author_sort Menezes, Luciana Gomes
collection PubMed
description OBJECTIVE: To investigate the acute effects of intravenous administration of cigarette smoke extract (CSE) on histological, inflammatory, and respiratory function parameters in rats, as well as to compare this potential acute lung injury (ALI) model with that with the use of oleic acid (OA). METHODS: We studied 72 Wistar rats, divided into four groups: control (those injected intravenously with saline); CSE (those injected intravenously with CSE and saline); OA (those injected intravenously with saline and OA); and CSE/OA (those injected intravenously with CSE and OA). RESULTS: Mean lung compliance was significantly lower in the OA and CSE/OA groups (2.12 ± 1.13 mL/cmH(2)O and 1.82 ± 0.77 mL/cmH(2)O, respectively)than in the control group (3.67 ± 1.38 mL/cmH(2)O). In bronchoalveolar lavage fluid, the proportion of neutrophils was significantly higher in the OA and CSE/OA groups than in the control group, as was the activity of metalloproteinases 2 and 9. Pulmonary involvement, as assessed by morphometry, was significantly more severe in the OA and CSE/OA groups (72.9 ± 13.8% and 77.6 ± 18.0%, respectively) than in the control and CSE groups (8.7 ± 4.1% and 32.7 ± 13.1%, respectively), and that involvement was significantly more severe in the CSE group than in the control group. CONCLUSIONS: The intravenous administration of CSE, at the doses and timing employed in this study, was associated with minimal ALI. The use of CSE did not potentiate OA-induced ALI. Additional studies are needed in order to clarify the potential role of this model as a method for studying the mechanisms of smoking-induced lung injury.
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spelling pubmed-40758062014-07-16 Acute lung injury induced by the intravenous administration of cigarette smoke extract Menezes, Luciana Gomes Uzuelli, Juliana Alves Tefé-Silva, Cristiane Ramos, Simone Gusmão dos Santos, José Eduardo Tanus Martinez, José Antônio Baddini J Bras Pneumol Original Article OBJECTIVE: To investigate the acute effects of intravenous administration of cigarette smoke extract (CSE) on histological, inflammatory, and respiratory function parameters in rats, as well as to compare this potential acute lung injury (ALI) model with that with the use of oleic acid (OA). METHODS: We studied 72 Wistar rats, divided into four groups: control (those injected intravenously with saline); CSE (those injected intravenously with CSE and saline); OA (those injected intravenously with saline and OA); and CSE/OA (those injected intravenously with CSE and OA). RESULTS: Mean lung compliance was significantly lower in the OA and CSE/OA groups (2.12 ± 1.13 mL/cmH(2)O and 1.82 ± 0.77 mL/cmH(2)O, respectively)than in the control group (3.67 ± 1.38 mL/cmH(2)O). In bronchoalveolar lavage fluid, the proportion of neutrophils was significantly higher in the OA and CSE/OA groups than in the control group, as was the activity of metalloproteinases 2 and 9. Pulmonary involvement, as assessed by morphometry, was significantly more severe in the OA and CSE/OA groups (72.9 ± 13.8% and 77.6 ± 18.0%, respectively) than in the control and CSE groups (8.7 ± 4.1% and 32.7 ± 13.1%, respectively), and that involvement was significantly more severe in the CSE group than in the control group. CONCLUSIONS: The intravenous administration of CSE, at the doses and timing employed in this study, was associated with minimal ALI. The use of CSE did not potentiate OA-induced ALI. Additional studies are needed in order to clarify the potential role of this model as a method for studying the mechanisms of smoking-induced lung injury. Sociedade Brasileira de Pneumologia e Tisiologia 2013 /pmc/articles/PMC4075806/ /pubmed/23503484 http://dx.doi.org/10.1590/S1806-37132013000100006 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Menezes, Luciana Gomes
Uzuelli, Juliana Alves
Tefé-Silva, Cristiane
Ramos, Simone Gusmão
dos Santos, José Eduardo Tanus
Martinez, José Antônio Baddini
Acute lung injury induced by the intravenous administration of cigarette smoke extract
title Acute lung injury induced by the intravenous administration of cigarette smoke extract
title_full Acute lung injury induced by the intravenous administration of cigarette smoke extract
title_fullStr Acute lung injury induced by the intravenous administration of cigarette smoke extract
title_full_unstemmed Acute lung injury induced by the intravenous administration of cigarette smoke extract
title_short Acute lung injury induced by the intravenous administration of cigarette smoke extract
title_sort acute lung injury induced by the intravenous administration of cigarette smoke extract
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075806/
https://www.ncbi.nlm.nih.gov/pubmed/23503484
http://dx.doi.org/10.1590/S1806-37132013000100006
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