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J Appl Physiol (1985). 1987 Nov;63(5):2159-63.

Xanthine oxidase mediates elastase-induced injury to isolated lungs and endothelium.

Author information

1
Department of Medicine, University of Colorado Health Sciences Center, Denver 80262.

Abstract

Xanthine oxidase (XO)-generated toxic O2 metabolites appear to contribute to reperfusion injury, but the possibility that XO is involved in hyperoxic or neutrophil elastase-mediated injury has not been investigated. We found that lungs isolated from rats fed a tungsten-rich diet had negligible XO activities and after exposure to hyperoxia developed less acute edematous injury during perfusion with buffer or purified neutrophil elastase than XO-replete lungs from control rats which had been exposed to hyperoxia. In parallel, tungsten-treated XO-depleted cultured bovine pulmonary arterial endothelial cells made less superoxide anion and as monolayers leaked less 125I-labeled albumin after exposure to neutrophil elastase than XO-replete endothelial cell monolayers. Our findings suggest that XO-derived O2 metabolites contribute to acute edematous lung injury from hyperoxia directly and by enhancing susceptibility to neutrophil elastase.

PMID:
2826385
DOI:
10.1152/jappl.1987.63.5.2159
[Indexed for MEDLINE]

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