Impaired sodium excretion and increased blood pressure in mice with targeted deletion of renal epithelial insulin receptor

Proc Natl Acad Sci U S A. 2008 Apr 29;105(17):6469-74. doi: 10.1073/pnas.0711283105. Epub 2008 Apr 18.

Abstract

Renal tubule epithelial cells express the insulin receptor (IR); however, their value has not been firmly established. We generated mice with renal epithelial cell-specific knockout of the IR by Cre-recombinase-loxP recombination using a kidney-specific (Ksp) cadherin promoter. KO mice expressed significantly lower levels of IR mRNA and protein in kidney cortex (49-56% of the WT) and medulla (32-47%) homogenates. Immunofluorescence showed the greatest relative reduction in the thick ascending limb and collecting duct cell types. Body weight, kidney weight, and food and water intakes were not different from WT littermates. However, KO mice had significantly increased basal systolic blood pressure (BP, 15 mm Hg higher) as measured by radiotelemetry. In response to a volume load by gavage (20 ml/kg of body weight, 0.9% NaCl, 15% dextrose), KO mice had impaired natriuresis (37 +/- 10 versus 99 +/- 9 mmol of Na(+) per 2 h in WT). Furthermore, volume load led to a sustained increase in BP in KO mice only. In contrast, insulin administration i.p. (0.5 units/kg of body weight) resulted in a significant fall in BP in WT, but not in KO mice. To test the role of reduced renal nitric oxide (NO) production in these responses, basal urinary nitrates plus nitrites excretion (UNOx) was measured and found to be 61% lower in KO vs. WT mice. Furthermore, acute insulin increased UNOx by 202% in the WT, relative to a significantly blunted rise (67%) in KO animals. These results illuminate a previously uncharacterized role for renal IR to reduce BP and facilitate sodium and water excretion, possibly via NO production.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Gene Deletion*
  • Gene Expression Regulation / drug effects
  • Gene Targeting*
  • Insulin / administration & dosage
  • Insulin / pharmacology
  • Integrases / metabolism
  • Kidney Medulla / cytology
  • Kidney Medulla / drug effects
  • Kidney Medulla / metabolism
  • Kidney Tubules, Collecting / cytology
  • Kidney Tubules, Collecting / drug effects
  • Kidney Tubules, Collecting / metabolism*
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Natriuresis / drug effects
  • Nitrates / urine
  • Nitrites / urine
  • Organ Specificity / drug effects
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor, Insulin / genetics*
  • Receptor, Insulin / metabolism
  • Reproducibility of Results
  • Sodium / urine*

Substances

  • Insulin
  • Nitrates
  • Nitrites
  • RNA, Messenger
  • Sodium
  • Receptor, Insulin
  • Cre recombinase
  • Integrases