Restrained whole body plethysmography for measure of strain-specific and allergen-induced airway responsiveness in conscious mice

J Appl Physiol (1985). 2006 Nov;101(5):1495-505. doi: 10.1152/japplphysiol.00464.2006. Epub 2006 Jul 20.

Abstract

The mouse is the most extensively studied animal species in respiratory research, yet the technologies available to assess airway function in conscious mice are not universally accepted. We hypothesized that whole body plethysmography employing noninvasive restraint (RWBP) could be used to quantify specific airway resistance (sRaw-RWBP) and airway responsiveness in conscious mice. Methacholine responses were compared using sRaw-RWBP vs. airway resistance by the forced oscillation technique (Raw-FOT) in groups of C57, A/J, and BALB/c mice. sRaw-RWBP was also compared with sRaw derived from double chamber plethysmography (sRaw-DCP) in BALB/c. Finally, airway responsiveness following allergen challenge in BALB/c was measured using RWBP. sRaw-RWBP in C57, A/J, and BALB/c mice was 0.51 +/- 0.03, 0.68 +/- 0.03, and 0.63 +/- 0.05 cm/s, respectively. sRaw derived from Raw-FOT and functional residual capacity (Raw*functional residual capacity) was 0.095 cm/s, approximately one-fifth of sRaw-RWBP in C57 mice. The intra- and interanimal coefficients of variations were similar between sRaw-RWBP (6.8 and 20.1%) and Raw-FOT (3.4 and 20.1%, respectively). The order of airway responsiveness employing sRaw-RWBP was AJ > BALBc > C57 and for Raw-FOT was AJ > BALB/c = C57. There was no difference between the airway responsiveness assessed by RWBP vs. DCP; however, baseline sRaw-RWBP was significantly lower than sRaw-DCP. Allergen challenge caused a progressive decrease in the provocative concentration of methacholine that increased sRaw to 175% postsaline values based on sRaw-RWBP. In conclusion, the technique of RWBP was rapid, reproducible, and easy to perform. Airway responsiveness measured using RWBP, DCP, and FOT was equivalent. Allergen responses could be followed longitudinally, which may provide greater insight into the pathogenesis of chronic airway disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Airway Resistance / drug effects
  • Airway Resistance / physiology*
  • Animals
  • Bronchial Provocation Tests
  • Bronchoconstrictor Agents / pharmacology*
  • Consciousness / physiology
  • Female
  • Forced Expiratory Flow Rates / physiology
  • Forced Expiratory Volume / drug effects
  • Methacholine Chloride / pharmacology*
  • Mice
  • Mice, Inbred Strains
  • Oscillometry
  • Plethysmography, Whole Body / instrumentation
  • Plethysmography, Whole Body / methods*
  • Restraint, Physical
  • Species Specificity
  • Specific Pathogen-Free Organisms

Substances

  • Bronchoconstrictor Agents
  • Methacholine Chloride