Expression of cyclooxygenase-2 in the juxtaglomerular apparatus of angiotensinogen gene-knockout mice

Nephron Physiol. 2006;102(1):p1-8. doi: 10.1159/000088312. Epub 2005 Sep 19.

Abstract

Aims: The present study was designed to examine the role of the renin-angiotensin system in the regulation of macula densa cyclooxygenase-2 (COX-2) during altered dietary salt intake.

Methods: We investigated COX-2 expression in the macula densa of angiotensinogen gene-knockout (Atg-/-) mice. COX-2 expression in the renal cortex was determined by real-time quantitative reverse transcription-polymerase chain reaction and immunohistochemistry.

Results: The renal cortical expression of COX-2 mRNA increased 24.7 times in Atg-/- mice compared with Atg+/+ mice. When Atg-/- mice were fed a high-salt diet (4% NaCl) for 10 days, the levels of COX-2 expression were markedly suppressed. The macula densa COX-2 immunoreactivity was correlated with the mRNA expression. The selective inhibition of neuronal isoform of nitric oxide synthase (N-NOS) activity by 7-nitroindazole significantly reduced the levels of COX-2 mRNA in Atg-/- mice by 54.1%.

Conclusion: These results suggest that (1) COX-2 activity in the macula densa can be regulated by salt intake through a mechanism independent of the renin-angiotensin system, and (2) COX-2 expression is functionally linked to renal cortical N-NOS activity in Atg-/- mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensinogen / genetics*
  • Animals
  • Blood Pressure
  • Creatinine / metabolism
  • Cyclooxygenase 2 / genetics*
  • Cyclooxygenase 2 / metabolism*
  • Enzyme Inhibitors / pharmacology
  • Female
  • Gene Expression Regulation, Enzymologic / drug effects
  • Indazoles / pharmacology
  • Juxtaglomerular Apparatus / enzymology*
  • Kidney Cortex / enzymology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Mice, Knockout
  • Nitric Oxide Synthase Type I / metabolism
  • Renin-Angiotensin System / physiology*
  • Sodium Chloride, Dietary / pharmacology

Substances

  • Enzyme Inhibitors
  • Indazoles
  • Sodium Chloride, Dietary
  • Angiotensinogen
  • Creatinine
  • Nitric Oxide Synthase Type I
  • Cyclooxygenase 2
  • 7-nitroindazole