Tepper J S, Costa D L, Lehmann J R, Weber M F, Hatch G E
NSI Technology Services Corporation, Environmental Sciences, Research Triangle Park, NC 27709.
Am Rev Respir Dis. 1989 Aug;140(2):493-501. doi: 10.1164/ajrccm/140.2.493.
Acute ozone (O3) exposure in humans produces changes in pulmonary function that attenuate with repeated exposure. This phenomenon, termed adaptation, has been produced in unanesthetized rats. Rats exposed to O3 (0, 0.35, 0.5, or 1.0 ppm) for 2.25 h for 5 consecutive days showed an increased frequency of breathing and a decreased tidal volume on Days 1 and 2 of exposure at all O3 concentrations. However, by Day 5 these breathing responses to O3 were diminished in rats exposed to 0.35 and 0.5 ppm, but not in rats exposed to 1.0 ppm. In addition, a flow limitation in smaller airways was observed after the second day of exposure to 0.5 ppm O3 that initially attenuated and then disappeared by the fifth day of exposure. In contrast to these findings, a light microscopic examination of fixed lung tissue sections from rats exposed to 0.5 ppm indicated a 5-day progressive pattern of epithelial damage and inflammation in the terminal bronchiolar region. A sustained 37% increase in lavageable protein was also observed over the course of the 5-day exposure regimen to 0.5 ppm. Lung glutathione increased initially, but it was within the control range on Days 4 and 5. Lung ascorbate was significantly elevated above control levels on Days 3 and 5. These data suggest that attenuation of the pulmonary function response to O3 occurs in laboratory rats with repeated exposure while biochemical and morphologic aspects of the tissue response continue to progress.
