Erythropoietin attenuates lung injury in lipopolysaccharide treated rats

J Surg Res. 2009 Jul;155(1):104-10. doi: 10.1016/j.jss.2008.10.003. Epub 2008 Nov 8.

Abstract

Background: Erythropoietin (EPO) elicits protective effects in lung ischemia-reperfusion, hyperoxia, acute necrotizing pancreatitis, and some other tissues. In the present study, we investigated the possible protective roles of EPO in the lipopolysaccharide (LPS) induced lung injury.

Materials and methods: Male Sprague-Dawley rats were treated with EPO (3000 U/kg, i.p.) or vehicle (saline), 30 min prior to LPS administration (6 mg/kg, i.v.). Four h following LPS injection, samples of pulmonary tissue were collected. Optical microscopy was performed to examine pathological changes in lungs. Validated methods were used to measure wet/dry ratios (W/D), myeloperoxidase (MPO) activity, malondialdehyde (MDA) concentrations, and nitrite/nitrate (NO(2)(-)/NO(3)(-)) levels in lungs. Western blotting was performed to study the pulmonary expression of inducible nitric oxide synthase (iNOS) and nitrotyrosine protein.

Results: Pretreatment with EPO led to (1) significant attenuation of endotoxemia induced evident lung histologic injury and edema; (2) inhibition of LPS mediated induction in MPO activity and MDA concentration; (3) inhibition of LPS mediated overproduction of pulmonary NO(2)(-)/NO(3)(-) levels; and (4) marked suppression in endotoxin induced expression of iNOS and nitrotyrosine.

Conclusions: This study provides considerable evidence that EPO has an ability to significantly attenuate endotoxin-induced acute lung injury in rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Erythropoietin / pharmacology
  • Erythropoietin / therapeutic use*
  • Lipopolysaccharides / toxicity
  • Lung / pathology
  • Lung Injury / chemically induced
  • Lung Injury / pathology
  • Lung Injury / prevention & control*
  • Male
  • Malondialdehyde / metabolism
  • Nitrates / metabolism
  • Nitric Oxide / biosynthesis*
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / metabolism*
  • Nitrites / metabolism
  • Peroxidase / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism

Substances

  • Lipopolysaccharides
  • Nitrates
  • Nitrites
  • Erythropoietin
  • Nitric Oxide
  • 3-nitrotyrosine
  • Tyrosine
  • Malondialdehyde
  • Peroxidase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat