During ozone (O-3) exposure, adult rats decrease their minute ventilation (
VE). To determine whether such changes are also observed in immature animal
s, Sprague-Dawley rats, aged 2, 4, 6, 8, or 12 wk, were exposed to O-3 (2 p
pm) in nose-only-exposure plethysmographs. Baseline VE normalized for body
weight decreased with age from 2.1 +/- 0.1 ml.min(-1).g(-1) in 2-wk-old rat
s to 0.72 +/- 0.03 ml.min(-1).g(-1) in 12-wk-old rats, consistent with the
higher metabolic rates of younger animals. In adult (8- and 12-wk-old) rats
, O-3 caused 40-50% decreases in VE that occurred primarily as the result o
f a decrease in tidal volume. In 6-wk-old rats, O-3-induced changes in VE w
ere significantly less, and in 2- and 4-wk-old rats, no significant changes
in VE were observed during O-3 exposure. The increased baseline VE and the
smaller decrements in VE induced by O-3 in the immature rats imply that th
eir delivered dose of O-3 is much higher than in adult rats. To determine w
hether these differences in O-3 dose influence the extent of injury, we mea
sured bronchoalveolar lavage protein concentrations. The magnitude of the c
hanges in bronchoalveolar lavage induced by O-3 was significantly greater i
n 2- than in 8-wk-old rats (267 +/- 47 vs. 165 +/- 22%, respectively, P < 0
.05). O-3 exposure also caused a significant increase in PGE(2) in a-wk-old
but not in adult rats. The results indicate that the ventilatory response
to O-3 is absent in a-wk-old rats and that lack of this response, in conjun
ction with a greater specific ventilation, leads to greater lung injury.