Inducible nitric oxide synthase modulates hydronephrosis following partial or complete unilateral ureteral obstruction in the neonatal mouse

Kee Hwan Yoo, Barbara A. Thornhill, Michael S. Forbes, Robert L. Chevalier

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

To investigate the role of endogenous inducible nitric oxide synthase (iNOS) in the response of the developing kidney to unilateral ureteral obstruction (UUO), neonatal iNOS null mutant (-/-) and wild-type (WT) mice were subjected to partial or complete UUO. At 7 and 21 days of age, apoptosis, renin, vascular endothelial growth factor (VEGF), fibroblasts (antifibroblast-specific peptide 1), myofibroblasts (α-smooth muscle actin), macrophages (F4/80), and collagen were measured in kidney tissue. Compared with WT, renal parenchymal thickness was increased, with preservation of the papilla, in -/- mice with partial UUO, but decreased in -/- mice with complete UUO. Ureteral peristalsis increased with severity of pelvic dilatation in WT, and increased further in -/- mice with partial UUO. Apoptosis, fibroblasts, and macrophages were increased in -/- mice with complete UUO, but there was no effect of iNOS on other histological parameters following complete UUO. Renin was decreased in -/- mice with partial UUO. There was no effect of iNOS genotype on renal collagen accumulation at either 7 or 21 days of age. These results are consistent with an injurious role for endogenous iNOS following partial UUO by inhibiting ureteral peristalsis and increasing renal renin although renal fibrosis is not affected. In contrast, in mice with complete UUO, iNOS attenuates apoptosis and enhances renal parenchymal thickness. Alterations in the severity of ureteral obstruction may therefore influence the effect of iNOS on long-term renal injury.

Original languageEnglish
JournalAmerican Journal of Physiology - Renal Physiology
Volume298
Issue number1
DOIs
Publication statusPublished - 2010 Jan 1

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Ureteral Obstruction
Hydronephrosis
Nitric Oxide Synthase Type II
Kidney
Renin
Peristalsis
Apoptosis
Collagen
Fibroblasts
Macrophages
Myofibroblasts
Vascular Endothelial Growth Factor A
Smooth Muscle
Actins
Dilatation
Fibrosis
Genotype

Keywords

  • Apoptosis
  • Collagen
  • Fibrosis
  • Macrophages
  • Ureteral peristalsis

ASJC Scopus subject areas

  • Physiology
  • Urology

Cite this

Inducible nitric oxide synthase modulates hydronephrosis following partial or complete unilateral ureteral obstruction in the neonatal mouse. / Yoo, Kee Hwan; Thornhill, Barbara A.; Forbes, Michael S.; Chevalier, Robert L.

In: American Journal of Physiology - Renal Physiology, Vol. 298, No. 1, 01.01.2010.

Research output: Contribution to journalArticle

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