Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study

Detalhes bibliográficos
Autor(a) principal: Palma Kuhl, Cristiana
Data de Publicação: 2014
Outros Autores: Alves Garcez, Tuane Nerissa, Bileski Magrisso, Alessandra, Fernandes Correia Laurino, Claudia Cilene, Obino Cirne-Lima, Elizabeth, Rieken Macedo Rocco, Patricia, Vieira de Macedo Neto, Amarilio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinical and Biomedical Research
Texto Completo: https://seer.ufrgs.br/index.php/hcpa/article/view/48676
Resumo: Introduction: Mouse models of emphysema are important tools for testing different therapeutic strategies. The aim of this study was to develop a mouse model of emphysema induced by different doses of elastase in order to produce different degrees of severity. Methods: Thirty female mice (C57BL/6) were used in this study. Different doses of porcine pancreatic elastase were administered intratracheally once a week for four weeks, as follows: 0.1 U (n=8), 0.15 U (n=7), and 0.2 U (n=7). Control mice (n=8) received 50 microL of sterile saline solution intratracheally. Lung mechanics were analyzed by plethysmography. Mean linear intercept and volume fraction occupied by collagen and elastic fibers were determined. Results: An increase in lung resistance was observed with 0.2 U of elastase [median (P-25-P75): 2.02 (1.67; 2.34) cmH2O.s/mL], as well as a decrease in tidal volume and minute ventilation. Peak expiratory flow increased significantly in the groups treated with 0.15 U and 0.2 U of elastase. Mean linear intercept was higher with 0.15 U and 0.2 U of elastase, with destruction of alveolar walls [median (P-25-P75): 30.31 (26.65-43.13) microm and 49.49 (31.67-57.71) microm respectively]. The volume fraction occupied by collagen and elastic fibers was lower in the group receiving 0.2 U of elastase. Conclusion: Four intratracheal instillations of 0.2 U of elastase once a week induced changes in lung function and histology, producing an experimental model of severe pulmonary emphysema, whereas 0.15 U resulted in only histological changes.
id UFRGS-20_a20efac2616a6566f5a85d382da0559d
oai_identifier_str oai:seer.ufrgs.br:article/48676
network_acronym_str UFRGS-20
network_name_str Clinical and Biomedical Research
repository_id_str
spelling Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental studyDevelopment of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental studyenfisema pulmonar, mecânica pulmonar, elastase pancreática.Pulmonary emphysemaLung mechanicsPancreatic elastase.Introduction: Mouse models of emphysema are important tools for testing different therapeutic strategies. The aim of this study was to develop a mouse model of emphysema induced by different doses of elastase in order to produce different degrees of severity. Methods: Thirty female mice (C57BL/6) were used in this study. Different doses of porcine pancreatic elastase were administered intratracheally once a week for four weeks, as follows: 0.1 U (n=8), 0.15 U (n=7), and 0.2 U (n=7). Control mice (n=8) received 50 microL of sterile saline solution intratracheally. Lung mechanics were analyzed by plethysmography. Mean linear intercept and volume fraction occupied by collagen and elastic fibers were determined. Results: An increase in lung resistance was observed with 0.2 U of elastase [median (P-25-P75): 2.02 (1.67; 2.34) cmH2O.s/mL], as well as a decrease in tidal volume and minute ventilation. Peak expiratory flow increased significantly in the groups treated with 0.15 U and 0.2 U of elastase. Mean linear intercept was higher with 0.15 U and 0.2 U of elastase, with destruction of alveolar walls [median (P-25-P75): 30.31 (26.65-43.13) microm and 49.49 (31.67-57.71) microm respectively]. The volume fraction occupied by collagen and elastic fibers was lower in the group receiving 0.2 U of elastase. Conclusion: Four intratracheal instillations of 0.2 U of elastase once a week induced changes in lung function and histology, producing an experimental model of severe pulmonary emphysema, whereas 0.15 U resulted in only histological changes.Introduction: Mouse models of emphysema are important tools for testing different therapeutic strategies. The aim of this study was to develop a mouse model of emphysema induced by different doses of elastase in order to produce different degrees of severity.Methods: Thirty female mice (C57BL/6) were used in this study. Different doses of porcine pancreatic elastase were administered intratracheally once a week for four weeks, as follows: 0.1 U (n=8), 0.15 U (n=7), and 0.2 U (n=7). Control mice (n=8) received 50 microL of sterile saline solution intratracheally. Lung mechanics were analyzed by plethysmography. Mean linear intercept and volume fraction occupied by collagen and elastic fibers were determined.Results: An increase in lung resistance was observed with 0.2 U of elastase [median (P-25-P75): 2.02 (1.67; 2.34) cmH2O.s/mL], as well as a decrease in tidal volume and minute ventilation. Peak expiratory flow increased significantly in the groups treated with 0.15 U and 0.2 U of elastase. Mean linear intercept was higher with 0.15 U and 0.2 U of elastase, with destruction of alveolar walls [median (P-25-P75): 30.31 (26.65-43.13) microm and 49.49 (31.67-57.71) microm respectively]. The volume fraction occupied by collagen and elastic fibers was lower in the group receiving 0.2 U of elastase.Conclusion: Four intratracheal instillations of 0.2 U of elastase once a week induced changes in lung function and histology, producing an experimental model of severe pulmonary emphysema, whereas 0.15 U resulted in only histological changes.HCPA/FAMED/UFRGS2014-10-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer-reviewed ArticleAvaliado por Paresapplication/pdfhttps://seer.ufrgs.br/index.php/hcpa/article/view/48676Clinical & Biomedical Research; Vol. 34 No. 3 (2014): Clinical and Biomedical ResearchClinical and Biomedical Research; v. 34 n. 3 (2014): Clinical and Biomedical Research2357-9730reponame:Clinical and Biomedical Researchinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSenghttps://seer.ufrgs.br/index.php/hcpa/article/view/48676/31850Palma Kuhl, CristianaAlves Garcez, Tuane NerissaBileski Magrisso, AlessandraFernandes Correia Laurino, Claudia CileneObino Cirne-Lima, ElizabethRieken Macedo Rocco, PatriciaVieira de Macedo Neto, Amarilioinfo:eu-repo/semantics/openAccess2024-01-19T13:30:54Zoai:seer.ufrgs.br:article/48676Revistahttps://www.seer.ufrgs.br/index.php/hcpaPUBhttps://seer.ufrgs.br/index.php/hcpa/oai||cbr@hcpa.edu.br2357-97302357-9730opendoar:2024-01-19T13:30:54Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.none.fl_str_mv Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental studyenfisema pulmonar, mecânica pulmonar, elastase pancreática.
title Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
spellingShingle Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
Palma Kuhl, Cristiana
Pulmonary emphysema
Lung mechanics
Pancreatic elastase.
title_short Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
title_full Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
title_fullStr Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
title_full_unstemmed Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
title_sort Development of different degrees of elastase-induced emphysema in mice: a randomized controlled experimental study
author Palma Kuhl, Cristiana
author_facet Palma Kuhl, Cristiana
Alves Garcez, Tuane Nerissa
Bileski Magrisso, Alessandra
Fernandes Correia Laurino, Claudia Cilene
Obino Cirne-Lima, Elizabeth
Rieken Macedo Rocco, Patricia
Vieira de Macedo Neto, Amarilio
author_role author
author2 Alves Garcez, Tuane Nerissa
Bileski Magrisso, Alessandra
Fernandes Correia Laurino, Claudia Cilene
Obino Cirne-Lima, Elizabeth
Rieken Macedo Rocco, Patricia
Vieira de Macedo Neto, Amarilio
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Palma Kuhl, Cristiana
Alves Garcez, Tuane Nerissa
Bileski Magrisso, Alessandra
Fernandes Correia Laurino, Claudia Cilene
Obino Cirne-Lima, Elizabeth
Rieken Macedo Rocco, Patricia
Vieira de Macedo Neto, Amarilio
dc.subject.por.fl_str_mv Pulmonary emphysema
Lung mechanics
Pancreatic elastase.
topic Pulmonary emphysema
Lung mechanics
Pancreatic elastase.
description Introduction: Mouse models of emphysema are important tools for testing different therapeutic strategies. The aim of this study was to develop a mouse model of emphysema induced by different doses of elastase in order to produce different degrees of severity. Methods: Thirty female mice (C57BL/6) were used in this study. Different doses of porcine pancreatic elastase were administered intratracheally once a week for four weeks, as follows: 0.1 U (n=8), 0.15 U (n=7), and 0.2 U (n=7). Control mice (n=8) received 50 microL of sterile saline solution intratracheally. Lung mechanics were analyzed by plethysmography. Mean linear intercept and volume fraction occupied by collagen and elastic fibers were determined. Results: An increase in lung resistance was observed with 0.2 U of elastase [median (P-25-P75): 2.02 (1.67; 2.34) cmH2O.s/mL], as well as a decrease in tidal volume and minute ventilation. Peak expiratory flow increased significantly in the groups treated with 0.15 U and 0.2 U of elastase. Mean linear intercept was higher with 0.15 U and 0.2 U of elastase, with destruction of alveolar walls [median (P-25-P75): 30.31 (26.65-43.13) microm and 49.49 (31.67-57.71) microm respectively]. The volume fraction occupied by collagen and elastic fibers was lower in the group receiving 0.2 U of elastase. Conclusion: Four intratracheal instillations of 0.2 U of elastase once a week induced changes in lung function and histology, producing an experimental model of severe pulmonary emphysema, whereas 0.15 U resulted in only histological changes.
publishDate 2014
dc.date.none.fl_str_mv 2014-10-07
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Avaliado por Pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/48676
url https://seer.ufrgs.br/index.php/hcpa/article/view/48676
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/48676/31850
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv HCPA/FAMED/UFRGS
publisher.none.fl_str_mv HCPA/FAMED/UFRGS
dc.source.none.fl_str_mv Clinical & Biomedical Research; Vol. 34 No. 3 (2014): Clinical and Biomedical Research
Clinical and Biomedical Research; v. 34 n. 3 (2014): Clinical and Biomedical Research
2357-9730
reponame:Clinical and Biomedical Research
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Clinical and Biomedical Research
collection Clinical and Biomedical Research
repository.name.fl_str_mv Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv ||cbr@hcpa.edu.br
_version_ 1799767053658226688