Acid aspiration-induced lung inflammation and injury are exacerbated in NADPH oxidase-deficient mice

• Published in: American journal of physiology. Lung cellular and molecular physiology Vol. 292; no. 3; p. L760
• Main Authors: Segal, Brahm H, Davidson, Bruce A, Hutson, Alan D, Russo, Thomas A, Holm, Bruce A, Mullan, Barbara, Habitzruther, Michael, Holland, Steven M, Knight, 3rd, Paul R
• Format: Journal Article
• Language: English
• Published: United States 01-03-2007
• Subjects: Acids - metabolism; Animals; Capillary Permeability; Chemokines - metabolism; Cytokines - metabolism; Drainage - methods; Female; Hyperoxia; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; NADPH Oxidases - deficiency; NADPH Oxidases - genetics; NADPH Oxidases - physiology; Neutrophil Infiltration; Phagocytes - cytology; Phagocytes - metabolism; Pneumonia - enzymology; Pneumonia - etiology; Pneumonia - pathology
• ISSN: 1040-0605
• DOI: 10.1152/ajplung.00281.2006

Increased reactive oxidant intermediates (ROIs) from primed leukocytes have been implicated in the pathogenesis of acid aspiration lung injury. To evaluate the specific role of the phagocyte NADPH oxidase-derived ROIs in acid lung injury, the p47phox-/- knockout mouse model of chronic granulomatous disease was used. p47phox-/- mice developed a significantly greater alveolar neutrophilic leukocytosis compared with wild-type mice at all time points after acid injury, with the difference between genotypes being most marked at 48 h. In contrast, the p47phox-/- mice had a decreased number of macrophages in bronchoalveolar lavage (BAL) compared with wild-type at 48 h after acid or saline aspiration. Albumin concentration in BAL reflecting capillary leak was also greater in p47phox-/- compared with wild-type mice. BAL concentrations of proinflammatory cytokines and chemokines were greater in p47phox-/- compared with wild-type mice. These findings suggest that NADPH oxidase, directly or indirectly, plays a role in attenuating the acute neutrophilic response after acid lung injury. We speculate that this downmodulating effect may be mediated by promoting the transition from production of cytokines and chemokines involved in neutrophilic infiltration to a less injurious, chronic inflammatory response.