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   <subfield code="a">Intercellular adhesion molecule-1 contributes to pulmonary oxygen toxicity in mice: Role of leukocytes revised</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Craig Wegner, Walter Wolyniec, April LaPlante, Kristin Marschman, Klaus Lubbe, Nancy Haynes, Robert Rothlein, L. Letts]</subfield>
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   <subfield code="a">In immature or injured lungs, impaired alveolar gas exchange forces the use of elevated levels of inhaled oxygen to maintain life. But, at high concentrations oxygen induces lung injury, edema, and bronchopulmonary dysplasia, probably by stimulating the generation of reactive oxygen radicals and subsequent neutrophil infiltration. In addition to regulating neutrophil diapedesis, intercellular adhesion molecule-1 (ICAM-1) expression is marked on inflamed alveolar epithelium, suggesting a role for ICAM-1 in oxygen-induced, neutrophil-mediated parenchymal damage. To test this, we evaluated the rat anti-mouse ICAM-1 monoclonal antibody YN 1/1.7 in 2 protocols of oxygen-induced toxicity in adult, male Balb-c mice: ≥95% O2 for 84 hr and ≥95% O2 for 60 hr followed by 48 hr at 21% (ambient) O2. YN1/1.7 treatment partially attenuated the neutrophil infiltration, lung damage (lavage lactate dehydrogenase [LDH] activity) and dysfunction (reductions in respiratory system compliance [Crs] and diffusion capacity of the lungs for carbon monoxide [DLco] in the 84 hr exposure protocol. In the milder 60 hr exposure protocol, YN1/1.7 completely blocked the oxygen-induced lung dysfunction (reductions in Crs and DLco). These results confirm the contribution of leukocytes in the pathogenesis of pulmonary oxygen toxicity and indicate that antagonism of ICAM-1 may provide a therapeutic approach to reducing hyperoxic lung injury and dysfunction.</subfield>
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   <subfield code="a">Springer-Verlag New York Inc., 1992</subfield>
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   <subfield code="a">Cell adhesion</subfield>
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   <subfield code="a">Neutrophils</subfield>
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   <subfield code="a">Acute lung injury</subfield>
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   <subfield code="u">Department of Pharmacology, Boehringer Ingelheim Pharmaceuticals, Inc., 90 East Ridge, P.O. Box 368, 06877, Ridgefield, CT, USA</subfield>
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   <subfield code="u">Department of Pharmacology, Boehringer Ingelheim Pharmaceuticals, Inc., 90 East Ridge, P.O. Box 368, 06877, Ridgefield, CT, USA</subfield>
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   <subfield code="a">LaPlante</subfield>
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   <subfield code="a">Haynes</subfield>
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   <subfield code="u">Department of Immunology, Boehringer Ingelheim Pharmaceuticals, Inc., 90 East Ridge, P.O. Box 368, 06877, Ridgefield, CT, USA</subfield>
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