Reperfusion of ischemic skeletal muscle causes erythrocyte hemolysis and decreases subsequent oxidant-mediated lung injury

J Lab Clin Med. 1991 Oct;118(4):352-8.

Abstract

A prior transient hindlimb ischemia/reperfusion (I/R) insult decreased acute lung injury in rats subsequently treated with cobra venom factor. I/R-mediated protection was associated with erythrocyte hemolysis, increased plasma catalase activity, and increased plasma hydrogen peroxide scavenging activity. In contrast, hindlimb I/R did not increase lung catalase activity, and large amounts of injected catalase were required to increase lung catalase activity. The results suggest that limited I/R in one organ can induce systemic processes that may decrease a subsequent O2 metabolite-mediated injury in another distant organ. The mechanism may involve release of catalase from hemolyzed erythrocytes at levels that are not sufficient to measurably increase total lung catalase activity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Catalase / analysis
  • Catalase / blood
  • Elapid Venoms / pharmacology
  • Erythrocytes / pathology
  • Erythrocytes / physiology*
  • Hemolysis / physiology*
  • Hydrogen Peroxide / blood
  • Lung / chemistry
  • Lung / enzymology
  • Lung Injury*
  • Male
  • Muscles / blood supply*
  • Muscles / metabolism
  • Muscles / pathology
  • Oxidants / pharmacology*
  • Oxygen / metabolism
  • Pulmonary Edema / chemically induced
  • Pulmonary Edema / pathology
  • Pulmonary Edema / prevention & control*
  • Rats
  • Rats, Inbred Strains
  • Reperfusion Injury / complications
  • Reperfusion Injury / pathology
  • Reperfusion Injury / physiopathology*

Substances

  • Elapid Venoms
  • Oxidants
  • cobra venom factor
  • Hydrogen Peroxide
  • Catalase
  • Oxygen