N-Acetyl-β-D-Glucosaminidase Activity in Bronchoalveolar Lavage Fluid: Characterization and Response to Ozone Exposure

Acute exposure of humans to 0.4 ppm ozone results in reversible respiratory function decrements, and cellular and biochemical changes leading to the production of substances which can mediate inflammation and acute lung injury. While pulmonary function decrements occur almost immediately after ozone exposure, it is not known how quickly the cellular and biochemical changes indicative of inflammation occur in humans. Changes in neutrophils and PGE2 have been observed in humans as early as 3 hr (28) and as late as 18 hr post exposure (19). The purpose of this study was to determine whether inflammatory changes occur relatively rapidly (within 1 hr) following exposure to ozone, or if the cascade of events which are initiated by ozone and lead to inflammation, take some time to develop. We exposed 10 healthy volunteers twice: once to filtered air and once to 0.4 ppm ozone. Each exposure lasted for 2 hr at an exercise level of 60 L/min, and bronchoalveolar lavage was performed 1 hr following exposure. The data from this study were compared to those from a previous study in which 10 subjects were exposed to O3 under identical conditions except that bronchoalveolar lavage was performed 18 hr following exposure. The results of the present study demonstrate that O3 is capable of inducing rapid cellular and biochemical changes in the lung. These changes were detectable as early as 1 hr following a 2 hr exposure of humans to ozone. The profiles of these changes were different at 1 hr and 18 hr following ozone exposures. Bronchoalveolar lavage fluid had levels of neutrophils, IL-6, and prostaglandin E2 that were higher at 1 hr than at 18 hr post exposure. On the other hand, the levels of fibronectin and plasminogen activator were found to be higher at 18 hr than at 1 hr after ozone exposure. A temporal association appeared to exist between changes occurring in the biochemical markers and alterations in lung function. Further studies may be useful in determining if a causal relationship exists between these parameters.

Download Full-text

Ozone reduces murine alveolar and peritoneal macrophage phagocytosis: the role of prostanoids

AJP Lung Cellular and Molecular Physiology ◽

10.1152/ajplung.1991.261.4.l277 ◽

1991 ◽

Vol 261 (4) ◽

pp. L277-L282 ◽

Cited By ~ 6

Author(s):

B. J. Canning ◽

R. R. Hmieleski ◽

E. W. Spannhake ◽

G. J. Jakab

Keyword(s):

Bronchoalveolar Lavage ◽

Peritoneal Macrophage ◽

Phagocytic Activity ◽

Bronchoalveolar Lavage Fluid ◽

Lavage Fluid ◽

Peritoneal Macrophages ◽

Ozone Exposure ◽

Cyclooxygenase Inhibitors ◽

Macrophage Phagocytosis

Continuous ozone exposure (0.5 ppm, 1–14 days) reduced the phagocytic activity of murine alveolar and peritoneal macrophages. The response of peritoneal macrophages to ozone was virtually indistinguishable from the response of alveolar macrophages. When added exogenously, prostaglandin E2 (PGE2) inhibited alveolar and peritoneal macrophage phagocytosis. To test the hypothesis that prostanoids mediated the effects of ozone on macrophages, PGE levels of bronchoalveolar lavage fluid (BALF) and the phagocytic activity of macrophages from ozone-exposed mice pretreated with cyclooxygenase inhibitors were measured. PGE levels in BALF were increased following ozone exposure, with high levels of PGE associated with large decreases in phagocytic activity. Pretreatment with indomethacin and d-naproxen completely inhibited ozone-induced increases in PGE recovered by BAL and the suppression of peritoneal macrophage phagocytic activity. The inactive enantiomer of naproxen, l-naproxen, was without effect. Indomethacin partially inhibited ozone-induced suppression of alveolar macrophage phagocytic activity. These observations suggest that prostanoids play a key role in the response to ozone.

Download Full-text