Effects of endothelin-1 and endothelin-1-receptor blockade on renal function in humans

Nephrol Dial Transplant. 2004 Nov;19(11):2742-6. doi: 10.1093/ndt/gfh471. Epub 2004 Aug 24.

Abstract

Background: In patients with renal or cardiac failure, renal function may be endangered by elevated plasma concentrations of the vasoconstrictor endothelin-1 (ET-1). To mimic effects of pathologically increased plasma ET-1, we gave intravenous ET-1 in healthy subjects and examined whether simultaneous infusion of the ETA-receptor antagonist VML 588 would prevent the effects of ET-1 on the kidney.

Methods: Nine healthy men received on four separate days intravenous infusion of ET-1 (2.5 ng/kg/min) superimposed on vehicle (saline) or on VML 588 infusion (0.05, 0.20 and 0.40 mg/kg/h) in randomized order to assess the effects on renal function and renal haemodynamics.

Results: At resting plasma ET-1, infusion of VML 588 alone had no significant effects on renal function. Infusion of ET-1 alone decreased glomerular filtration rate by 11% and this reduction was not reversed by co-infusion of VML 588. ET-1 reduced renal blood flow by 35% and VML 588 reduced this decrease by one-third, in a dose-independent fashion. ET-1 increased the filtration fraction by 34% and VML 588 reduced this increase dose-independently by one-half. ET-1 increased renal vascular resistance by 59% and VML 588 reduced this increase dose-independently by one-half. Finally, ET-1 decreased sodium excretion by 58% and VML 588 reduced this decrease dose-independently by two-thirds.

Conclusions: ET-1-induced reductions in renal function were partially but not completely prevented in a dose-independent manner by the ETA-receptor antagonist VML 588.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Dioxanes / pharmacology*
  • Endothelin Receptor Antagonists*
  • Endothelin-1 / blood
  • Endothelin-1 / pharmacology
  • Endothelin-1 / physiology*
  • Glomerular Filtration Rate
  • Humans
  • Kidney / drug effects
  • Kidney / physiology*
  • Male
  • Pyridines
  • Pyrimidines / pharmacology*
  • Sulfonamides
  • Tetrazoles

Substances

  • Dioxanes
  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Pyridines
  • Pyrimidines
  • Sulfonamides
  • Tetrazoles
  • clazosentan