Acute mechanical forces cause deterioration in lung structure and function in elastase-induced emphysema

Am J Physiol Lung Cell Mol Physiol. 2012 Oct 1;303(7):L567-74. doi: 10.1152/ajplung.00217.2012. Epub 2012 Aug 3.

Abstract

The relation between the progression of chronic obstructive pulmonary disease (COPD) and exacerbations is unclear. Currently, no animal model of acute exacerbation of COPD (AECOPD) exists. The objectives of this study were to evaluate the effects of mechanical forces induced by deep inspirations (DIs) on short-term deterioration of lung structure and function to mimic AECOPD. At 2, 7, or 21 days after treatment with elastase, mice were ventilated with or without DIs (35 cmH(2)O airway pressure for 3 s, 2 times/min) for 1 h. Functional residual capacity (FRC) was measured with body plethysmography, and respiratory compliance, resistance, and hysteresivity were obtained via forced oscillations. From hematoxylin and eosin-stained sections, equivalent airspace diameters (D), alveolar wall thickness (W(t)), number of septal ruptures (N(sr)), and attachment density (A(d)) around airways were determined. FRC, compliance, and hysteresivity statistically significantly increased with time, and both increased due to DIs. Interestingly, DIs also had an effect on FRC, compliance, resistance, and hysteresivity in control mice. The development of emphysema statistically significantly increased D and W(t) in time, and the DIs caused subtle differences in D. At 21 days, the application of DIs changed the distribution of D, increased W(t) and N(sr), and decreased A(d). These results suggest that once a critical remodeling of the parenchyma has been reached, acute mechanical forces lead to irreversible changes in structure and function, mimicking COPD exacerbations. Thus, the acute application of DIs in mice with emphysema may serve as a useful model of AECOPD.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Airway Resistance / drug effects
  • Animals
  • Disease Models, Animal
  • Disease Progression
  • Lung Compliance / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Pancreatic Elastase / pharmacology
  • Pulmonary Disease, Chronic Obstructive / chemically induced
  • Pulmonary Disease, Chronic Obstructive / pathology*
  • Pulmonary Disease, Chronic Obstructive / physiopathology*
  • Pulmonary Emphysema / chemically induced
  • Pulmonary Emphysema / pathology*
  • Pulmonary Emphysema / physiopathology*
  • Respiratory Function Tests

Substances

  • Pancreatic Elastase