4.5 Article

Lung volumes and respiratory mechanics in elastase-induced emphysema in mice

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 105, Issue 6, Pages 1864-1872

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.90924.2008

Keywords

elastance; airway resistance; pressure-volume curve; airway reopening; crackle sound

Funding

  1. Hungarian Scientific Research Fund [T42971, T37810, 67700]
  2. National Health and Medical Research Council of Australia [139024]
  3. National Science Foundation [BES-0402530]
  4. National Heart, Lung, and Blood Institute [HL-059215]

Ask authors/readers for more resources

Hantos Z, Adamicza A, Janosi TZ, Szabari MV, Tolnai J, Suki B. Lung volumes and respiratory mechanics in elastase-induced emphysema in mice. J Appl Physiol 105: 1864-1872, 2008. First published October 9, 2008; doi:10.1152/japplphysiol.90924.2008.-Absolute lung volumes such as functional residual capacity, residual volume (RV), and total lung capacity (TLC) are used to characterize emphysema in patients, whereas in animal models of emphysema, the mechanical parameters are invariably obtained as a function of transrespiratory pressure (Prs). The aim of the present study was to establish a link between the mechanical parameters including tissue elastance (H) and airway resistance (Raw), and thoracic gas volume (TGV) in addition to Prs in a mouse model of emphysema. Using low-frequency forced oscillations during slow deep inflation, we tracked H and Raw as functions of TGV and Prs in normal mice and mice treated with porcine pancreatic elastase. The presence of emphysema was confirmed by morphometric analysis of histological slices. The treatment resulted in an increase in TGV by 51 and 44% and a decrease in H by 57 and 27%, respectively, at 0 and 20 cmH(2)O of Prs. The Raw did not differ between the groups at any value of Prs, but it was significantly higher in the treated mice at comparable TGV values. In further groups of mice, tracheal sounds were recorded during inflations from RV to TLC. All lung volumes but RV were significantly elevated in the treated mice, whereas the numbers and size distributions of inspiratory crackles were not different, suggesting that the airways were not affected by the elastase treatment. These findings emphasize the importance of absolute lung volumes and indicate that tissue destruction was not associated with airway dysfunction in this mouse model of emphysema.

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