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Oxygen toxicity: augmentation of antioxidant defense mechanisms in rat lung.

Abstract
In studies directed at determining the activities of selected enzymes in lung tissue after in vivo exposure to hyperoxia, 70-day-old rats were exposed to 85% or 90% O2 for 1-14 days. After 7 days of exposure to 90% O2 (1atm), superoxide dismutase activities in mitochondrial and cytosolic fractions increased, respectively, to 245 and 145% of control; glutathione peroxidase, glutathione reductase, and glucose-6-phosphate dehydrogenase activities increased, respectively, to 317, 175, and 413% of control. The levels of reduced glutathione and total nonprotein sulfhydryl compounds were elevated to 195% and 365% of control. Similar changes were observed in rats exposed to 85% O2 for up to 14 days, but to a lesser degree. The changes are interpreted as a reflection of the overall magnitude of oxidant-induced lung injury-reparative processes. The results suggest that hyperoxia induces an increase in lung "antioxidant" defense capabilities. This apparent adaptive response may be important in decreasing the susceptibility of lung tissue to continued O2 toxicity.
AuthorsR E Kimball, K Reddy, T H Peirce, L W Schwartz, M G Mustafa, C E Cross
JournalThe American journal of physiology (Am J Physiol) Vol. 230 Issue 5 Pg. 1425-31 (May 1976) ISSN: 0002-9513 [Print] United States
PMID1275087 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Sulfhydryl Compounds
  • Glucosephosphate Dehydrogenase
  • Peroxidases
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione Reductase
  • Glutathione
  • Oxygen
Topics
  • Animals
  • Body Weight
  • Bronchi (ultrastructure)
  • Epithelial Cells
  • Epithelium (ultrastructure)
  • Glucosephosphate Dehydrogenase (metabolism)
  • Glutathione (metabolism)
  • Glutathione Peroxidase (metabolism)
  • Glutathione Reductase (metabolism)
  • Lung (enzymology, pathology)
  • Male
  • Oxygen (toxicity)
  • Peroxidases (metabolism)
  • Rats
  • Starvation
  • Sulfhydryl Compounds (metabolism)
  • Superoxide Dismutase (metabolism)

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