Temporal evolution of epithelial, vascular and interstitial lung injury in an experimental model of idiopathic pulmonary fibrosis induced by butyl-hydroxytoluene


Autoria(s): PARRA, Edwin Roger; BOUFELLI, Gabriela; BERTANHA, Fernanda; SAMORANO, Luciana de Paula; AGUIAR JR., Armando Costa; COSTA, Fernanda Magalhaes Arantes; CAPELOZZI, Vera Luiza; BARBAS-FILHO, Joao Valente
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

This study was undertaken to test whether the structural remodelling of pulmonary parenchyma can be sequentially altered in a model and method that demonstrate the progression of the disease and result in remodelling within the lungs that is typical of idiopathic pulmonary fibrosis. Three groups of mice were studied: (i) animals that received 3-5-di-tert-butyl-4-hydroxytoluene (BHT) and were killed after 2 weeks (early BHT = 9); (ii) animals that received BHT and were killed after 4 weeks (late BHT = 11); (iii) animals that received corn oil solution (control = 10). The mice were placed in a ventilated Plexiglas chamber with a mixture of pure humidified oxygen and compressed air. Lung histological sections underwent haematoxylin-eosin, immunohistochemistry (epithelial, endothelial and immune cells) and specific staining (collagen/elastic fibres) methods for morphometric analysis. When compared with the control group, early BHT and late BHT groups showed significant decrease of type II pneumocytes, lower vascular density in both and higher endothelial activity. CD4 was increased in late BHT compared with early and control groups, while CD8, macrophage and neutrophil cells were more prominent only in early BHT. The collagenous fibre density were significantly higher only in late BHT, whereas elastic fibre content in late BHT was lower than that in control group. We conclude that the BHT experimental model is pathologically very similar to human usual interstitial pneumonia. This feature is important in the identification of animal models of idiopathic pulmonary fibrosis that can accurately reflect the pathogenesis and progression of the human disease.

National Council for Scientific and Technological Development (CNPq)

Foundation for the Support of Research of the State of Sao Paulo (FAPESP)

Universidade de São Paulo - Laboratories for Medical Research[LIM-05] - FM/USP

Hospital das Clinicas

University of Sao Paulo Medical School (USP)

Identificador

INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, v.89, n.5, p.350-357, 2008

0959-9673

http://producao.usp.br/handle/BDPI/25210

10.1111/j.1365-2613.2008.00600.x

http://dx.doi.org/10.1111/j.1365-2613.2008.00600.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

International Journal of Experimental Pathology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #BHT experimental model #collagen/elastic system #endothelial activity #idiopathic pulmonary fibrosis #microvascular density #type II pneumocytes #usual interstitial pneumonia #MURINE MODEL #MAJOR TYPES #PNEUMONIA #BLEOMYCIN #MICE #MECHANICS #PATHOGENESIS #COLLAGEN #FIBERS #DAMAGE #Pathology
Tipo

article

original article

publishedVersion