The Journal of urology · 2003
Cyclooxygenase-2 up-regulation in reflux nephropathy.
СтатьяНазвание и аннотация: Перевод в очереди
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Solari Valeria, Piotrowska Anna Piaseczna, Cascio Salvatore, Unemoto Kei, Chertin Boris, Puri Prem
Аннотация
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.
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.
Предметные рубрики MeSH
Blotting, WesternChildChild, PreschoolCyclooxygenase 2FemaleGene Expression Regulation, EnzymologicHumansHypertension, RenalInfantIsoenzymesKidney Failure, ChronicKidney Tubules, ProximalMaleMembrane ProteinsNephritis, InterstitialProstaglandin-Endoperoxide SynthasesReference ValuesReverse Transcriptase Polymerase Chain ReactionUp-RegulationVesico-Ureteral Reflux