Asialoerythropoietin has strong renoprotective effects against ischemia-reperfusion injury in a murine model

Transplantation. 2007 Aug 27;84(4):504-10. doi: 10.1097/01.tp.0000277672.02783.33.

Abstract

Background: The renoprotective effect of erythropoietin (EPO) and the nonhematopoietic EPO, asialoEPO was investigated in a murine ischemia-reperfusion injury (I/R) model.

Methods: I/R was created by clamping the right renal pedicle for 60 min after left nephrectomy. Balb/c mice were divided into four groups (n=15 in each group): sham operation (Sham), vehicle treatment (Vehicle), EPO treatment (EPO), and asialoEPO treatment (AsialoEPO). EPO and asialoEPO were given at a dose of 500 IU/kg 30 min before I/R. Plasma creatinine (Cr), survival, and the number of apoptotic cells were analyzed. Protein expression was analyzed by Western blotting.

Results: Plasma Cr level was not significantly different at 6 hr after I/R. At 24 hr after I/R, the Cr (mg/dL) levels in Sham, Vehicle, EPO, and asialoEPO were 0.13+/-0.01, 1.24+/-0.70, 0.24+/-0.08, and 0.25+/-0.13, respectively (P<0.05). The numbers of apoptotic cells in these groups were 0.1+/-0.1, 98.9+/-42.6, 3.3+/-0.7, and 2.9+/-1.6, respectively (P<0.05). Western blotting revealed that in kidney tissue of mice treated with EPO and asialoEPO, p38-MAPK and the proapoptotic molecule Bad was decreased, and the antiapoptotic molecules Bcl-xL and XIAP were increased. Survival rates at 7 days after I/R injury in the Sham, Vehicle, EPO, and AsialoEPO groups were 100%, 21.4%, 23.1%, and 53.8%, respectively (P=0.05).

Conclusion: EPO and asialoEPO attenuated renal dysfunction caused by I/R in mouse kidney at the same level, but only asialoEPO improved survival.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Asialoglycoproteins / therapeutic use*
  • Creatinine / blood
  • Disease Models, Animal
  • Erythropoietin / analogs & derivatives*
  • Erythropoietin / therapeutic use
  • Female
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney / physiopathology*
  • Mice
  • Mice, Inbred BALB C
  • Random Allocation
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*
  • Survival Rate
  • X-Linked Inhibitor of Apoptosis Protein / metabolism
  • bcl-Associated Death Protein / antagonists & inhibitors
  • bcl-X Protein / metabolism
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors

Substances

  • Asialoglycoproteins
  • Bad protein, mouse
  • Bcl2l1 protein, mouse
  • X-Linked Inhibitor of Apoptosis Protein
  • asialoerythropoietin
  • bcl-Associated Death Protein
  • bcl-X Protein
  • Erythropoietin
  • Creatinine
  • p38 Mitogen-Activated Protein Kinases