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Departments of 1 Physiology, 2 Pediatrics, and 3 Obstetrics and Gynecology and Perinatal Research Centre, University of Alberta, Edmonton, Alberta T6G 2S2, Canada
Hyperoxic exposure of rat pups during alveolarization (postnatal days 4-14) severely retards alveolar development. Some aspects of this inhibition are mediated by leukotrienes (LTs) and may be time sensitive. We determined 1) the effects of exposure to hyperoxia (O2) during discrete periods before and during alveolarization on developing alveoli and 2) whether a relationship exists between O2 and LTs in these periods. Pups were exposed to >95% O2 from days 1 to 4, 4 to 9, 9 to 14, or 4 to 14 in the absence and presence of the LT synthesis inhibitor MK-0591. Both the level of in vitro lung tissue LT output on days 4, 9, and 14 and the degree of alveolarization on day 14 were determined. Pups exposed to O2 from days 4 to 9 had a more profound inhibition of alveolarization on day 14 compared with those exposed to O2 from days 1 to 4 or 9 to 14. Peptido-LT levels were significantly higher in pups exposed to O2 on days 9 and 14 compared with pups in air and returned to normal once normoxia was restored. LT inhibition from days 4 to 14, 4 to 9, or 9 to 14 in pups exposed to O2 from days 4 to 14 prevented the O2-induced inhibition of alveolarization. These data suggest that developing alveoli are sensitive to LTs shortly before and after day 9, significantly retarding certain parameters of alveolarization on day 14. We conclude that some of the effects of O2 are not uniform throughout different stages of alveolarization and that this is likely related to the timing of LT exposure.
MK-0591; morphometry; 5-lipoxygenase-activating protein
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