Characterization of pulmonary function parameters in mice will facilit
ate the dissection of genetic mechanisms underlying airway hyperrespon
siveness We evaluated acetylcholine (ACh)-induced respiratory system r
esistance (Rrs) and elastance (Ers) in A/J and C3H/HeJ mice and compar
ed these results with the previously used airway pressure-time index (
APTI). A low-dead-space ventilatory system was designed to ventilate a
nesthetized mice with constant inspiratory flow. The end-inflation occ
lusion method was used to measure Rrs and Ers at baseline and after in
travenous ACh (12.5-75.0 mu g/kg) challenge. ACh induced a dose-depend
ent rise in Rrs and Ers in A/J mice, whereas minimal changes were obse
rved in C3H/HeJ mice. A/J mice had a higher baseline Rrs, yet the resp
onse to ACh was independent of baseline Rrs. Additionally, sequential
ACh challenges led to augmented responses. Rrs, Ers, and APTI were str
ongly correlated, and each was useful to detect differences in interst
rain cholinergic-induced airway responsiveness. The Rrs detected the s
mallest differences between the strains of mice studied.