Cyclooxygenase-2 up-regulation in reflux nephropathy

J Urol. 2003 Oct;170(4 Pt 2):1624-7. doi: 10.1097/01.ju.0000085810.37816.65.

Abstract

Purpose: Reflux nephropathy (RN) is a major cause of end stage renal failure in children and hypertension is a frequent complication. Cyclooxygenase-2 (COX-2) is an enzyme responsible for the prostaglandin synthesis. It has been shown that COX-2 up-regulates renin production leading to renovascular hypertension. We investigate COX-2 expression in the kidneys of children with RN.

Materials and methods: Kidney specimens from 12 patients 2 to 13 years old with severe RN secondary to primary high grade vesicoureteral reflux obtained at the time of nephrectomy and 5 controls were examined. Single labeled immunohistochemistry was performed with 2 COX-2 antibodies using light and confocal microscopy. Quantification of COX-2 was determined by Western blotting analysis. COX-2 gene expression was evaluated by real-time quantitative reverse transcription polymerase chain reaction.

Results: There was a strong COX-2 immunoreactivity in the proximal tubules and tubulointerstitial space in the RN samples compared to controls. Immunoreactive COX-2 protein expression was markedly increased in RN samples compared to controls. Real-time reverse transcription polymerase chain reaction showed a significant increase in COX-2 mRNA expression in the RN samples compared to controls (p <0.05).

Conclusions: Over expression of COX-2 in reflux nephropathy suggests that COX-2 may be involved in the pathogenesis of tubulointerstitial damage associated with severe reflux nephropathy.

MeSH terms

  • Blotting, Western
  • Child
  • Child, Preschool
  • Cyclooxygenase 2
  • Female
  • Gene Expression Regulation, Enzymologic
  • Humans
  • Hypertension, Renal / genetics*
  • Hypertension, Renal / pathology
  • Infant
  • Isoenzymes / genetics*
  • Kidney Failure, Chronic / genetics*
  • Kidney Failure, Chronic / pathology
  • Kidney Tubules, Proximal / enzymology
  • Kidney Tubules, Proximal / pathology
  • Male
  • Membrane Proteins
  • Nephritis, Interstitial / genetics*
  • Nephritis, Interstitial / pathology
  • Prostaglandin-Endoperoxide Synthases / genetics*
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation / genetics
  • Vesico-Ureteral Reflux / genetics*
  • Vesico-Ureteral Reflux / pathology

Substances

  • Isoenzymes
  • Membrane Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases