4.3 Article

Establishment and evaluation of chronic obstructive pulmonary disease model by chronic exposure to motor vehicle exhaust combined with lipopolysaccharide instillation

Journal

EXPERIMENTAL PHYSIOLOGY
Volume 103, Issue 11, Pages 1532-1542

Publisher

WILEY
DOI: 10.1113/EP087077

Keywords

chronic obstructive pulmonary disease; lipopolysaccharide; motor vehicle exhaust

Categories

Funding

  1. National Natural Science Foundation of China [81630004, 81470246, 81220108001, 81520108001, 81770043]
  2. Department of Science and Technology of China [2016YFC0903700, 2016YFC1304102]
  3. Changjiang Scholars and Innovative Research Teamin University [IRT0961]
  4. Guangdong Department of Science and Technology [2016A030311020, 2016A030313606]
  5. Guangzhou Department of Education Yangcheng Scholarship [12A001S]
  6. Guangzhou Department of Education Scholarship [1201630095]
  7. Ministry of Science and Technology of China [2015CB553406]
  8. Guangzhou Department of Science and Technology [2014Y2-00167, 201607010358]
  9. Guangdong Province Universities, Colleges Pearl River Scholar Funded Scheme of China

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Although it is well established that motor vehicle exhaust (MVE) has a close association with the occurrence and exacerbation of chronic obstructive pulmonary disease (COPD), very little is known about the combined effects of MVE and intermittent or chronic subclinical inflammation on COPD pathogenesis. Therefore, given the crucial role of inflammation in the development of COPD, we wanted to establish an animal model of COPD using both MVE exposure and airway inflammation, which could mimic the clinical pathological changes observed in COPD patients and greatly benefit the study of the molecular mechanisms of COPD. In the present study, we report that mice undergoing chronic exposure to MVE and intratracheal instillation of lipopolysaccharide (LPS) successfully established COPD, as characterized by persistent air flow limitation, airway inflammation, inflammatory cytokine production, emphysema and small airway remodelling. Moreover, the mice showed significant changes in ventricular and vascular pathology, including an increase in right ventricular pressure, right ventricular hypertrophy and remodelling of pulmonary arterial walls. We have thus established a new mouse COPD model by combining chronic MVE exposure with early intratracheal instillation of LPS, which will allow us to study the relationship between air pollution and the development of COPD and to investigate the underlying molecular mechanisms.

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