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1 Institute for Pediatric Urology, Department of Urology, Weill Cornell Medical Center, New York, NY, USA
2 Department of Pathology, Weill Cornell Medical Center, New York, NY, USA
* To whom correspondence should be addressed. E-mail: dfelsen{at}med.cornell.edu.
Progression of renal damage after relief of unilateral ureteral obstruction [UUO] has been demonstrated, especially in neonatal rats. We evaluated renal function and renal damage after relief of 3-day UUO in five groups of adult rats. Group 1, no treatment. Group 2, 3-day UUO.
Groups 3 - 5, 3-day UUO followed by relief. Group 3, 7-day relief; Group 4, 14-day relief; Group 5, 28-day relief. Glomerular filtration rate (GFR), renal blood flow (RBF), tissue transforming growth factor-
[TGF-
], interstitial fibrosis and fibroblast expression, tubular
apoptosis, macrophage infiltration, expression of nitric oxide synthases (NOS), and urinary nitrate/nitrite (NO2/NO3) were evaluated. RBF and GFR were decreased to <10% of baseline by 3 days of UUO. GFR and RBF in previously obstructed kidney (POK) returned to
baseline by 14 days after relief. Both tissue TGF-
1 and interstitial fibrosis were significantly higher in POK of groups 3-5 compared to groups 1 and 2 . In group 5, the numbers of infiltrating macrophages, fibroblasts and apoptotic tubular cells were higher in POK compared
to group 1. Urinary NO2/NO3 was significantly higher than baseline from 3 to 27 days after
relief of UUO. Expression of NOS isoforms was increased in tubules. As interstitial fibrosis contributes to decreased renal function, these results suggest that the acute recovery in function may be compromised in the long term by the progressive renal fibrosis which was found. Furthermore, pharmacological intervention at the time of relief of UUO, targeted to fibrotic processes, may contribute to long term recovery of renal function.
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