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Pharmacological preconditioning with erythropoietin reduces ischemia-reperfusion injury in the small intestine of rats.

Abstract：

AIMS:Considering the implications that arose from several recent experimental studies using recombinant human erythropoietin in rodents, erythropoietin has been regarded as a pharmacological preconditioning agent. The purpose of the present study was to evaluate whether erythropoietin has a preconditioning effect against ischemia and reperfusion injury in the small intestine of the rat. MAIN METHODS:Intestinal ischemia was induced in male Wistar rats by clamping the superior mesenteric artery for 30 min, followed by reperfusion for 180 min. Recombinant human erythropoietin (1000 or 3000 U/kg) or vehicle was administered intraperitoneally 24 h prior to ischemia. After collection of ileal tissue, evaluation of damage was based on measurements of the accumulation of polymorphonuclear neutrophils by technetium-99m-labeled leukocyte uptake, content of malondialdehyde, reduced glutathione, contractile responses to agonists, and an evaluation of histopathological features in intestinal tissue. KEY FINDINGS:Treatment with erythropoietin 24 h before ischemia significantly reduced the tissue content of malondialdehyde and increased that of reduced glutathione. Pretreatment also significantly suppressed leukocyte infiltration into the postischemic tissue, as evidenced by the lower content of myeloperoxidase and technetium-99m-labeled leukocytes. Physiological and histopathological improvements were also significant with the rHuEpo treatment. SIGNIFICANCE:Results of the present study indicate that rHuEpo is an effective preconditioning agent in ischemic injury of the small intestine. Protection provided by recombinant human erythropoietin is closely related to the inhibition of oxidative stress and leukocyte infiltration, which might be among the possible protective mechanisms of erythropoietin in intestinal ischemia and reperfusion.

journal_name

Life Sci

journal_title

Life sciences

authors

Sayan H,Ozacmak VH,Sen F,Cabuk M,Atik DY,Igdem AA,Ozacmak ID

doi

10.1016/j.lfs.2008.12.025

subject

Has Abstract

pub_date

2009-03-13 00:00:00

pages

364-71

issue

11-12

eissn

0024-3205

issn

1879-0631

pii

S0024-3205(09)00034-4

journal_volume

84

pub_type

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