Abstract

Male Fischer 344 rats were exposed to a simulated urban profile of ozone (O 3) (9-hr ramped spike, integrated concentration = 0.19 ppm) for up to 78 weeks. Small, but statistically significant, changes in breathing patterns and mechanics in unanesthetized, restrained rats were observed at Weeks 1, 3, 13, 52, and 78 during postexposure challenge with 0, 4, and 8% carbon dioxide (CO 2). The data indicate that O 3 exposure caused an overall increase in expiratory resistance ( R e), but particularly at 78 weeks. This increase in R e most likely accounts for the rats' reduced ability to increase ventilation during CO 2 challenge compared to control rats. Reductions in CO 2-induced tidal volume increases were observed in all O 3-exposed animals during postexposure challenges to 4 and 8% CO 2. Cumulatively, over all time points, spontaneous frequency of breathing and CO 2-induced hyperventilation were also reduced. The decrease in frequency was dependent on a significant increase in the inspiratory time relative to control without a change in expiratory time. Light microscopic evaluation of the lung did not reveal any lesions associated with O 3 exposure at any time point. Although statistically significant effects were detected, the etiology of the above-mentioned functional changes remains speculative. The potential relevance of these data to acute and chronic O 3 exposure in humans is also discussed.

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