Korean J Nephrol.  2005 Mar;24(2):191-203.

The Effect of alpha-MSH on Long-term Histologic Changes after Acute Ischemic Kidney Injury in Rats

Affiliations
  • 1Department of Internal Medicine, Eulji Medical College, Seoul, Korea.
  • 2Department of Internal Medicine, College of Medicine, Korea University, Seoul, Korea. wonyong@korea.ac.kr
  • 3Department of Pathology, The Institute of Renal Disease, College of Medicine, Korea University, Seoul, Korea.

Abstract

BACKGROUND
Ischemic acute renal failure (ARF) is increasingly recognized as involving chronic functional and structural sequelae. Ischemia reperfusion injury (I/R) plays a major role in delayed graft function and long-term changes after kidney transplantation, also. The present study was designed to evaluate the long-term changes after acute ischemic injury and whether renoprotection by alpha-MSH in the acute ischemic stage, could reduce the long-term sequelae. METHODS: In control group, ischemia/reperfusion injury was induced in male Sprague-Dawley rats by clamping Lt. renal pedicle for 15, 45, 60 minutes after removal of Rt. Kidney and followed by reperfusion. The animals in alpha-MSH group were injected alpha-MSH prior to reperfusion and then every day for 1 week. We measured BUN, creatinine at 24 hour after I/R injury, and in each group, 6 animals were sacrified at 1 week and 4 weeks after I/R injury to evaluate apoptosis, ED1, PCNA, and histopathologic changes. RESULTS: At 4 weeks after I/R injury, the remnant structural damage such as apoptosis, ED1 stained cells, MT (+) tubulointerstitial fibrosis were observed. alpha-MSH could reduce the initial functional injury, and apoptosis, ED1 stained monocyte, MT (+) tubulointerstitial fibrosis, also. CONCLUSION: Renal function was recoverd at 4 weeks after I/R injury, but structural sequelae such as apoptosis, fibrosis were remnant. alpha-MSH could attenuate initial functional damage and remnant fibrosis.

Keyword

Ischemia/reperfusion injury; Long- term sequelae; alpha-MSH; Reference

MeSH Terms

Acute Kidney Injury
alpha-MSH*
Animals
Apoptosis
Constriction
Creatinine
Delayed Graft Function
Fibrosis
Humans
Kidney Transplantation
Kidney*
Male
Monocytes
Proliferating Cell Nuclear Antigen
Rats*
Rats, Sprague-Dawley
Reperfusion
Reperfusion Injury
Creatinine
Proliferating Cell Nuclear Antigen
alpha-MSH
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