Literature DB >> 9730866

Relationship of inhaled ozone concentration to acute tracheobronchial epithelial injury, site-specific ozone dose, and glutathione depletion in rhesus monkeys.

C G Plopper1, G E Hatch, V Wong, X Duan, A J Weir, B K Tarkington, R B Devlin, S Becker, A R Buckpitt.   

Abstract

Acute pulmonary epithelial injury produced by short-term exposure to ozone varies by site within the tracheobronchial tree. To test whether this variability is related to the local dose of ozone at the tissue site or to local concentrations of glutathione, we exposed adult male rhesus monkeys for 2 h to filtered air or to 0.4 or 1.0 ppm ozone generated from 18O2. Following exposure, lungs were split into lobes and specimens were selected by microdissection so that measurements could be made on airway tissue of similar branching history, including trachea, proximal (generation one or two) and distal (generation six or seven) intrapulmonary bronchi, and proximal respiratory bronchioles. One half of the lung was lavaged for analysis of extracellular components. In monkeys exposed to filtered air, the concentration of reduced glutathione (GSH) varied throughout the airway tree, with the proximal intrapulmonary bronchus having the lowest concentration and the parenchyma having the highest concentration. Exposure to 1.0 ppm ozone significantly reduced GSH only in the respiratory bronchiole, whereas exposure to 0.4 ppm increased GSH only in the proximal intrapulmonary bronchus. Local ozone dose (measured as excess 18O) varied by as much as a factor of three in different airways of monkeys exposed to 1.0 ppm, with respiratory bronchioles having the highest concentration and the parenchyma the lowest concentration. In monkeys exposed to 0.4 ppm, the ozone dose was 60% to 70% less than in the same site in monkeys exposed to 1.0 ppm. Epithelial disruption was present to some degree in all airway sites, but not in the parenchyma, in animals exposed to 1.0 ppm ozone. The mass of mucous and ciliated cells decreased in all airways, and necrotic and inflammatory cells increased. At 0.4 ppm, epithelial injury was minimal, except in the respiratory bronchiole, where cell loss and necrosis occurred, and was 50% that found in monkeys exposed to 1.0 ppm ozone. We conclude that there is a close association between site-specific O3 dose, the degree of epithelial injury, and glutathione depletion at local sites in the tracheobronchial tree.

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Year:  1998        PMID: 9730866     DOI: 10.1165/ajrcmb.19.3.3183

Source DB:  PubMed          Journal:  Am J Respir Cell Mol Biol        ISSN: 1044-1549            Impact factor:   6.914


  15 in total

Review 1.  Promotion of cardiovascular disease by exposure to the air pollutant ozone.

Authors:  Marsha P Cole; Bruce A Freeman
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2009-06-12       Impact factor: 5.464

2.  Ozone-induced airway epithelial cell death, the neurokinin-1 receptor pathway, and the postnatal developing lung.

Authors:  Shannon R Murphy; Karen L Oslund; Dallas M Hyde; Lisa A Miller; Laura S Van Winkle; Edward S Schelegle
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-07-25       Impact factor: 5.464

3.  Progress in assessing air pollutant risks from in vitro exposures: matching ozone dose and effect in human airway cells.

Authors:  Gary E Hatch; Kelly E Duncan; David Diaz-Sanchez; Michael T Schmitt; Andrew J Ghio; Martha Sue Carraway; John McKee; Lisa A Dailey; Jon Berntsen; Robert B Devlin
Journal:  Toxicol Sci       Date:  2014-06-13       Impact factor: 4.849

4.  Persistent rhinitis and epithelial remodeling induced by cyclic ozone exposure in the nasal airways of infant monkeys.

Authors:  Stephan A Carey; Carol A Ballinger; Charles G Plopper; Ruth J McDonald; Alfred A Bartolucci; Edward M Postlethwait; Jack R Harkema
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2010-12-03       Impact factor: 5.464

5.  Role of surfactant protein-A (SP-A) in lung injury in response to acute ozone exposure of SP-A deficient mice.

Authors:  Rizwanul Haque; Todd M Umstead; Padmavathi Ponnuru; Xiaoxuan Guo; Samuel Hawgood; David S Phelps; Joanna Floros
Journal:  Toxicol Appl Pharmacol       Date:  2006-12-23       Impact factor: 4.219

Review 6.  Utility of large-animal models of BPD: chronically ventilated preterm lambs.

Authors:  Kurt H Albertine
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2015-03-13       Impact factor: 5.464

7.  Airway and lung pathology due to mucosal surface dehydration in {beta}-epithelial Na+ channel-overexpressing mice: role of TNF-{alpha} and IL-4R{alpha} signaling, influence of neonatal development, and limited efficacy of glucocorticoid treatment.

Authors:  Alessandra Livraghi; Barbara R Grubb; Elizabeth J Hudson; Kristen J Wilkinson; John K Sheehan; Marcus A Mall; Wanda K O'Neal; Richard C Boucher; Scott H Randell
Journal:  J Immunol       Date:  2009-04-01       Impact factor: 5.422

8.  Interleukin (IL)-1 regulates ozone-enhanced tracheal smooth muscle responsiveness by increasing substance P (SP) production in intrinsic airway neurons of ferret.

Authors:  Z-X Wu; J S Barker; T P Batchelor; R D Dey
Journal:  Respir Physiol Neurobiol       Date:  2008-07-31       Impact factor: 1.931

9.  Ozone exposure alters serotonin and serotonin receptor expression in the developing lung.

Authors:  Shannon R Murphy; Edward S Schelegle; Lisa A Miller; Dallas M Hyde; Laura S Van Winkle
Journal:  Toxicol Sci       Date:  2013-04-09       Impact factor: 4.849

10.  Ozone-induced enhancement of airway hyperreactivity in rhesus macaques: Effects of antioxidant treatment.

Authors:  Cameron H Flayer; Erik D Larson; Anjali Joseph; Sean Kao; Wenxiu Qu; Austin Van Haren; Christopher M Royer; Lisa A Miller; John P Capitanio; Thais Sielecki; Melpo Christofidou-Solomidou; Angela Haczku
Journal:  J Allergy Clin Immunol       Date:  2019-10-15       Impact factor: 10.793

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