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Hemoglobin potentiates oxidant injury in isolated rat lungs.

Abstract
Isolated perfused rat lungs were subjected to oxidant injury induced by tert-butyl hydroperoxide (t-buOOH), which caused a significant increase in capillary permeability as assessed by the change in the capillary filtration coefficient. t-buOOH caused an increase in the change in the capillary filtration coefficient (delta Kfc) of 0.27 +/- 0.05 ml.min.cmH2O-1.100 g lung tissue-1 (mean +/- SE) that was accompanied by an increase in thiobarbituric acid reactive products of lipid peroxidation in the lung perfusate. The addition of hemoglobin to the perfusate potentiated t-buOOH-induced lung injury as evidenced by a significantly greater (P = 0.007) delta Kfc of 0.43 +/- 0.05. t-buOOH also caused hemoglobin to release large quantities of free iron in vitro. The potentiation of t-buOOH-induced lung injury by hemoglobin was prevented by apotransferrin as evidenced by a significant reduction (P = 0.001) in delta Kfc to 0.13 +/- 0.02. No statistically significant (P greater than 0.05) changes in segmental resistances or pulmonary vascular pressures occurred in any of the lungs injured with t-buOOH when compared with time controls. These results demonstrate that t-buOOH causes an oxidant injury in isolated rat lungs that can be potentiated by free iron released from hemoglobin.
AuthorsA F Seibert, A E Taylor, J B Bass, J Haynes Jr
JournalThe American journal of physiology (Am J Physiol) Vol. 260 Issue 6 Pt 2 Pg. H1980-4 (Jun 1991) ISSN: 0002-9513 [Print] United States
PMID2058730 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Apoproteins
  • Fenton's reagent
  • Hemoglobins
  • Membrane Lipids
  • Peroxides
  • Thiobarbiturates
  • Transferrin
  • apotransferrin
  • tert-Butylhydroperoxide
  • Hydrogen Peroxide
  • Iron
Topics
  • Animals
  • Apoproteins (physiology)
  • Capillary Permeability (drug effects)
  • Hemodynamics (drug effects)
  • Hemoglobins (metabolism, physiology)
  • Hydrogen Peroxide (metabolism)
  • In Vitro Techniques
  • Iron (metabolism)
  • Lipid Peroxidation
  • Lung (drug effects, metabolism)
  • Male
  • Membrane Lipids (metabolism)
  • Oxidation-Reduction
  • Peroxides (adverse effects)
  • Rats
  • Thiobarbiturates (metabolism)
  • Transferrin (physiology)
  • tert-Butylhydroperoxide

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