Early activation of cardiac and renal endothelin systems in experimental heart failure

Am J Physiol Heart Circ Physiol. 2003 Dec;285(6):H2482-91. doi: 10.1152/ajpheart.00419.2003.

Abstract

We investigated the time course of the expression of cardiac and renal endothelin systems in tachycardia-induced heart failure in dogs. Eleven beagles underwent rapid pacing at a progressively increased rate over a period of 5 wk, with a weekly clinical examination, echocardiography, measurement of circulating and urinary endothelin-1 (ET-1), and myocardial and renal tissue biopsies. Real-time quantitative PCR was used for determinations of tissue prepro-ET-1 (ppET-1), ET-1-converting enzyme (ECE-1), and ETA and ETB receptor mRNA. Cardiac and renal tissue ET-1 contents were evaluated by immunostaining and measured by radioimmunoassay at autopsy. Rapid pacing caused a progressive increase in end-systolic and end-diastolic ventricular volumes (P < 0.05) from week 2 together with a decrease in ejection fraction and in mean velocity of circumferential shortening (P < 0.05) from week 1. These changes were tightly correlated to myocardial ppET-1 and renal ETA receptor mRNA and less so to myocardial ECE-1 mRNA, and they occurred before any increase in plasma and urinary ET-1 (P < 0.05 from week 4) and clinical signs of heart failure. Renal ppET-1 did not change. Both cardiac and renal ET-1 peptide contents were increased at autopsy. We conclude that tachycardia-induced heart failure in dogs is characterized by an early activation of the cardiac and renal tissue endothelin systems, which occurs before any changes in circulating and urinary ET-1 and is closely related to altered ventricular function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aspartic Acid Endopeptidases / genetics
  • Aspartic Acid Endopeptidases / metabolism
  • Biopsy
  • Blood Pressure
  • Dogs
  • Endothelin-1 / blood
  • Endothelin-1 / genetics
  • Endothelin-1 / metabolism
  • Endothelin-1 / urine
  • Endothelin-Converting Enzymes
  • Gene Expression / physiology
  • Heart Failure / metabolism
  • Heart Failure / pathology
  • Heart Failure / physiopathology*
  • Heart Rate
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney / physiopathology*
  • Male
  • Metalloendopeptidases
  • Myocardium / metabolism*
  • Pacemaker, Artificial
  • Receptor, Endothelin A / genetics*
  • Receptor, Endothelin A / metabolism
  • Receptor, Endothelin B / genetics*
  • Receptor, Endothelin B / metabolism
  • Respiration

Substances

  • Endothelin-1
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Aspartic Acid Endopeptidases
  • Metalloendopeptidases
  • Endothelin-Converting Enzymes