Ischemic heart disease induces upregulation of endothelin receptor mRNA in human coronary arteries

Eur J Pharmacol. 2004 Jan 19;484(1):103-9. doi: 10.1016/j.ejphar.2003.11.001.

Abstract

Endothelin has been implicated in the pathogenesis of ischemic heart disease and congestive heart failure. The aims were to quantify endothelin type A (ETA) and type B (ETB) receptor mRNA levels in human coronary arteries from patients with ischemic heart disease, congestive heart failure and controls using real-time polymerase chain reaction (real-time PCR). In addition, the suitability of organ culture as a model mimicking endothelin receptor changes in cardiovascular disease was evaluated by in vitro pharmacology and real-time PCR. Endothelin ETA and ETB receptor mRNA levels were significantly higher in arteries from patients with ischemic heart disease (0.23+/-0.04 and 0.35+/-0.06) as compared to congestive heart failure (0.09+/-0.02 and 0.07+/-0.01) and controls (0.08+/-0.02 and 0.08+/-0.01). After organ culture, the endothelin ETB receptor mRNA levels were elevated, and the sarafotoxin 6c-induced vasoconstriction was more efficacious. Increased endothelin receptor activity may contribute to the increased vascular tone and development of atherosclerotic disease in ischemic heart disease in man.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coronary Vessels / drug effects
  • Coronary Vessels / metabolism*
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation
  • Heart Failure / genetics
  • Heart Failure / metabolism
  • Humans
  • In Vitro Techniques
  • Myocardial Ischemia / genetics
  • Myocardial Ischemia / metabolism
  • RNA, Messenger / agonists
  • RNA, Messenger / biosynthesis*
  • Receptor, Endothelin A / agonists
  • Receptor, Endothelin A / biosynthesis*
  • Receptor, Endothelin A / genetics
  • Receptor, Endothelin B / agonists
  • Receptor, Endothelin B / biosynthesis*
  • Receptor, Endothelin B / genetics
  • Up-Regulation / drug effects
  • Up-Regulation / physiology*

Substances

  • RNA, Messenger
  • Receptor, Endothelin A
  • Receptor, Endothelin B