Non-invasive diagnosis of early pulmonary disease in PECAM-deficient mice using infrared pulse oximetry

被引:12
作者
Early, Merideth A. [1 ]
Lishnevsky, Marta [1 ]
Gilchrist, John M. [1 ]
Higgins, David M. [1 ]
Orme, Ian M. [1 ]
Muller, William A. [1 ]
Gonzalez-Juarerro, Mercedes [1 ]
Schenkel, Alan R. [1 ]
机构
[1] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
基金
美国国家卫生研究院;
关键词
PECAM; Lung; Fibrosis; Blood; Oxygen; INTERSTITIAL PNEUMONIA; LEUKOCYTE EMIGRATION; SIGNAL-TRANSDUCTION; MOUSE STRAINS; PLATELET; APOPTOSIS; FIBROSIS; DESATURATION; MOLECULE; CD31;
D O I
10.1016/j.yexmp.2009.07.008
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Pulse oximetry is a common tool for detecting reduced pulmonary function in human interstitial lung diseases. It has not previously been used in a mouse model of interstitial lung disease. Further, platelet endothelial cell adhesion molecule deficient mice rarely show symptoms until disease is advanced. Using blood oxygen saturation, different stages of disease could be identified in a non-invasive manner. These stages could be correlated to pathology. Collagen deposition, using Picrosirius Red, did correlate with blood oxygen saturation. These studies are the first to show the use of an infrared pulse oximetry system to analyze the progression of a fibrotic interstitial lung disease in a mouse model of the human diseases. Further, these studies show that an early alveolar damage/enlargement event precedes the fibrosis in this mouse model, a stage that represents the best targets for disease analysis and prevention. This stage does not have extensive collagen deposition. Most importantly, targeting this earliest stage of disease for therapeutic intervention may lead to novel treatment for human disease. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 158
页数:7
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