Effect of specific and non-specific inhibition of COX-2 on renal oxygenation before and after water diuresis

Nephron Physiol. 2005;99(4):p101-4. doi: 10.1159/000083767. Epub 2005 Feb 3.

Abstract

Background/aims: Water diuresis usually increases medullary oxygenation as a result of increased medullary synthesis of prostaglandins, but it is not clear whether this involves activation of cyclooxygenase-1 (COX-1) or cyclooxygenase-2 (COX-2).

Methods: The effects of celecoxib, a selective inhibitor of COX-2, and of ibuprofen, a non-specific inhibitor of COX-1 and COX-2, upon renal oxygenation during water diuresis were studied in a double-blind, prospective manner in 13 young women (age 24-34 years) using blood-oxygen level dependent magnetic resonance imaging. Celecoxib 200 mg b.i.d. for 4 days was compared with ibuprofen 80 mg b.i.d. for 4 days and with a placebo.

Results: There was no effect of either drug on urinary volume, urinary osmolal concentration, or creatinine clearance. Water diuresis alone elicited a significant increase in oxygenation in borderline areas between cortex and medulla, which was eliminated by celecoxib or ibuprofen.

Conclusion: Renal medullary oxygenation is improved by water diuresis in normal young women in a way that is blocked by a selective inhibitor of COX-2 as well as non-selective cyclooxygenase inhibitors. Selective COX-2 may be expected to have significant effects on renal functions.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Body Water / metabolism*
  • Celecoxib
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase 2 Inhibitors / administration & dosage*
  • Diuresis / drug effects
  • Diuresis / physiology*
  • Double-Blind Method
  • Female
  • Humans
  • Kidney Medulla / drug effects
  • Kidney Medulla / metabolism*
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Oxygen / metabolism*
  • Oxygen Consumption / drug effects
  • Oxygen Consumption / physiology
  • Pyrazoles / administration & dosage*
  • Sulfonamides / administration & dosage*

Substances

  • Cyclooxygenase 2 Inhibitors
  • Membrane Proteins
  • Pyrazoles
  • Sulfonamides
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Celecoxib
  • Oxygen