The role of cyclooxygenases and prostanoid receptorsin furosemide-like salt losing tubulopathy: the hyperprostaglandin E syndrome

Acta Physiol Scand. 2004 Aug;181(4):523-8. doi: 10.1111/j.1365-201X.2004.01326.x.

Abstract

Hyperprostaglandin E syndrome/antenatal Bartter syndrome is characterized by NaCl wasting and volume depletion, juxtaglomerula hypertrophy, hyperreninism and secondary hyperaldosteronism. Primary causes are mutations in the gene for Na-K-2Cl-cotransporter, NKCC2, or for potassium channel, ROMK, responsible for medullary NaCl malabsorption. Most intriguing aspect of the syndrome is the association with a massively increased renal prostaglandin production which contributes substantially to the clinical picture of the patients. Therefore the term hyperprostaglandin E syndrome has been introduced. It is unclear how prostaglandins aggravate the NaCl transport deficiency. Aspects to prostaglandin synthesis and receptor-mediated function within the kidney in patients suffering from hyperprostaglandin E syndrome/antenatal Bartter syndrome will be discussed.

Publication types

  • Review

MeSH terms

  • Bartter Syndrome / physiopathology*
  • Diuresis
  • Humans
  • Kidney / metabolism
  • Prostaglandin-Endoperoxide Synthases / physiology*
  • Prostaglandins E / biosynthesis
  • Receptors, Prostaglandin E / physiology*

Substances

  • Prostaglandins E
  • Receptors, Prostaglandin E
  • Prostaglandin-Endoperoxide Synthases