4.4 Article

Age-dependent renal expression of acid-base transporters in neonatal ureter obstruction

Journal

PEDIATRIC NEPHROLOGY
Volume 24, Issue 8, Pages 1487-1500

Publisher

SPRINGER
DOI: 10.1007/s00467-009-1193-y

Keywords

Acid-base transporters; H+ excretion; HCO3- reabsorption; Impaired urinary acidification

Funding

  1. Danish National Research Foundation (Danmarks Grundforskningsfond)
  2. The Karen Elise Jensen Foundation
  3. The Commission of the European Union [QRLT-2000-00987, QLRT-200000778]
  4. The Human Frontier Science Program
  5. The WIRED program (Nordic Council and the Nordic Centre of Excellence Program in Molecular Medicine)
  6. The Novo Nordisk Foundation
  7. The Danish Medical Research Council
  8. The University of Aarhus
  9. The Korea Healthcare Technology RD Project
  10. Ministry of Health Welfare, Korea [A080143]
  11. Korea Health Promotion Institute [A080143] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Congenital obstructive nephropathy accounts for a major proportion of renal insufficiency in infancy and childhood. In an earlier investigation we demonstrated that bilateral complete ureteral obstruction (BUO) in rats is associated with inadequate urinary acidification [Am J Physiol Renal Physiol. 295(2):F497-506, 2008]. The aim of the study reported here was to determine whether this defect is also associated with unilateral ureteral obstruction (UUO), which is clinically more common than BUO. The time-course of the changes in protein expression levels of major renal acid-base transporters was examined at 7 and 14 weeks in rats with neonatally induced partial unilateral ureteral obstruction (PUUO), which was performed within the first 48 h of life. We observed that protein expression of the renal acid-base transporters NHE3, NBC1, NBCn1, pendrin and Na+-K+-ATPase was increased in both obstructed and non-obstructed kidneys 7 weeks after the induction of neonatal PUUO. This was confirmed by immunocytochemistry. In contrast, 14 weeks after the induction of PUUO, there was a significant downregulation of the renal acid-base transporters NBC1, NBCn1 and Na+-K+-ATPase in the obstructed kidneys. These time/age-dependent changes in protein expression were associated with parallel changes in renal function resulting in urine acidification in response to exogenous acid loading. In conclusion, these results show that downregulation of protein expression is a time/age-dependent response to PUUO, which could contribute to the decreased net acid excretion and development of metabolic acidosis in neonatal rats with PUUO.

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