2013•国际泌尿系统杂志Requires access

Protective effect of recombinant human erythropoietin on renal ischemia reperfusion injury in rats

Fangxin Qiu, Xiaopang Rao, Fang Tian

Open publisher page 0 citations

Abstract

Objectives To investigate protective effect of recombinant human erythropeietin (rhEPO) on acute renal ischemia-reperfusion injury(IR/I) in rats.Methods Twenty one male S-D rats were randomly divided into 3 groups:Sham,IR/I,rhEPO(injection via intraperitoneal 2 h before surgery at the dosages of 1000U/kg).Rat model of renal IR/I was established with clamping both pedicles for 45 min followed by reperfusion.Blood sample and kidneys were collected at indicated times.Serum creatinine levels,urea nitrogen,histological change and mortality were observed throughout the study.ELISA was used to measure the levels of serum vascular endothelial growth factor(VEGF).The expression of heme oxygenase-1 (HO-1) in kidney observed by Immunohistochemical.Results Extensive proximal tubular necrosis,functional impairment and higher mortality were found repeffusion after 24 hours in IR/I group (P < 0.01).Elevated serum VEGF levels and increased expression of HO-1 protein in kidney were significantly higher than IR/I group and sham group(P < 0.01).Conclusions thEPO can attenuate renal IR/I.The protection mechanisms may be through the anti-oxidation and to promote renal tubular epithelial cell regeneration. Key words: Reperfusion Injury;  Kidney;  failure ;  Rats;  Erythropoietion, Recombinant

About this research paper

What this paper is about

Objectives To investigate protective effect of recombinant human erythropeietin (rhEPO) on acute renal ischemia-reperfusion injury(IR/I) in rats.Methods Twenty one male S-D rats were randomly divided into 3 groups:Sham,IR/I,rhEPO(injection via intraperitoneal 2 h before surgery at the dosages of 1000U/kg).Rat model of renal IR/I was established with clamping both pedicles for 45 min followed by reperfusion.Blood sample and kidneys were collected at indicated times.Serum creatinine levels,urea nitrogen,histological change and mortality were observed throughout the study.ELISA was used to measure the levels of serum vascular endothelial growth factor(VEGF).The expression of heme oxygenase-1 (HO-1) in kidney observed by Immunohistochemical.Results Extensive proximal tubular necrosis,functional impairment and higher mortality were found repeffusion after 24 hours in IR/I group (P < 0.01).Elevated serum VEGF levels and increased expression of HO-1 protein in kidney were significantly higher than IR/I group and sham group(P < 0.01).Conclusions thEPO can attenuate renal IR/I.The protection mechanisms may be through the anti-oxidation and to promote renal tubular epithelial cell regeneration. Key words: Reperfusion Injury;  Kidney;  failure ;  Rats;  Erythropoietion, Recombinant

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objectives To investigate protective effect of recombinant human erythropeietin (rhEPO) on acute renal ischemia-reperfusion injury(IR/I) in rats.Methods Twenty one male S-D rats were randomly divided into 3 groups:Sham,IR/I,rhEPO(injection via intraperitoneal 2 h before surgery at the dosages of 1000U/kg).Rat model of renal IR/I was established with clamping both pedicles for 45 min followed by reperfusion.Blood sample and kidneys were collected at indicated times.Serum creatinine levels,urea nitrogen,histological change and mortality were observed throughout the study.ELISA was used to measure the levels of serum vascular endothelial growth factor(VEGF).The expression of heme oxygenase-1 (HO-1) in kidney observed by Immunohistochemical.Results Extensive proximal tubular necrosis,functional impairment and higher mortality were found repeffusion after 24 hours in IR/I group (P < 0.01).Elevated serum VEGF levels and increased expression of HO-1 protein in kidney were significantly higher than IR/I group and sham group(P < 0.01).Conclusions thEPO can attenuate renal IR/I.The protection mechanisms may be through the anti-oxidation and to promote renal tubular epithelial cell regeneration. Key words: Reperfusion Injury;  Kidney;  failure ;  Rats;  Erythropoietion, Recombinant

Key concepts: Erythropoietin, Kidney, Blood urea nitrogen, Creatinine, Medicine, Reperfusion injury, Vascular endothelial growth factor, Ischemia

Related papers

Back to paper searchBrowse research topicsOriginal source
Protective effect of recombinant human erythropoietin on renal ischemia reperfusion injury in rats — Research Paper | ScholarLens