Circulating endothelin-1 reduces splanchnic and renal blood flow and splanchnic glucose production in humans

J Appl Physiol (1985). 1995 Jul;79(1):141-5. doi: 10.1152/jappl.1995.79.1.141.

Abstract

The effect of minimal changes in circulating plasma endothelin-1 (ET-1) was studied in 12 healthy subjects receiving either 60 min of ET-1 (0.2 pmol.kg-1.min-1) or physiological saline intravenously. Blood was drawn from arterial, renal, and central hepatic vein catheters. Arterial ET-1-like immunoreactivity (ET-1-LI) increased from 4.7 +/- 0.4 (SE) to 8.6 +/- 1.0 pmol/l during ET-1 infusion. After 10 min, plasma ET-1-LI had increased to 6.12 +/- 0.29 pmol/l. For comparison the plasma ET-1-LI level was 12.9 +/- 4.2 pmol/in five patients with sepsis syndrome. Mean arterial blood pressure rose from 92 +/- 3 to 99 +/- 4 mmHg. Estimated splanchnic and renal blood flows fell by 18 +/- 5 and 10 +/- 3%, respectively, and splanchnic glucose production fell by 42 +/- 6% within 10 min of the ET-1 infusion and differed compared with corresponding control values. Only estimated splanchnic blood flow had increased 60 min after the ET-1 infusion. No change in splanchnic uptake of lactate or glycerol was seen. In conclusion, we suggest that circulating ET-1 with small or no demonstrable change in plasma concentration interferes with vasoactivity and splanchnic glycogenolyses in health and possibly pathophysiological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arteries
  • Blood Pressure / drug effects
  • Endothelins / blood*
  • Endothelins / pharmacology
  • Glucose / metabolism*
  • Glycerol / metabolism
  • Heart Rate / drug effects
  • Humans
  • Lactates / metabolism
  • Lactic Acid
  • Male
  • Oxygen Consumption / drug effects
  • Radioimmunoassay
  • Reference Values
  • Renal Circulation / drug effects
  • Renal Circulation / physiology*
  • Splanchnic Circulation / drug effects
  • Splanchnic Circulation / physiology*
  • Systemic Inflammatory Response Syndrome / blood
  • Systemic Inflammatory Response Syndrome / physiopathology
  • Viscera / metabolism

Substances

  • Endothelins
  • Lactates
  • Lactic Acid
  • Glucose
  • Glycerol