Endothelin ETA receptor antagonism in cardiovascular disease

Eur J Pharmacol. 2014 Aug 15:737:210-3. doi: 10.1016/j.ejphar.2014.05.046. Epub 2014 Jun 2.

Abstract

Since the discovery of the endothelin system in 1988, it has been implicated in numerous physiological and pathological phenomena. In the cardiovascular system, endothelin-1 (ET-1) acts through intracellular pathways of two endothelin receptors (ETA and ETB) located mainly on smooth muscle and endothelial cells to regulate vascular tone and provoke mitogenic and proinflammatory reactions. The endothelin ETA receptor is believed to play a pivotal role in the pathogenesis of several cardiovascular disease including systemic hypertension, pulmonary arterial hypertension (PAH), dilated cardiomyopathy, and diabetic microvascular dysfunction. Growing evidence from recent experimental and clinical studies indicates that the blockade of endothelin receptors, particularly the ETA subtype, grasps promise in the treatment of major cardiovascular pathologies. The simultaneous blockade of endothelin ETB receptors might not be advantageous, leading possibly to vasoconstriction and salt and water retentions. This review summarizes the role of ET-1 in cardiovascular modulation and the therapeutic potential of endothelin receptor antagonism.

Keywords: Cardiovascular disease; ET(A) receptor antagonists; Endothelin-1.

Publication types

  • Review

MeSH terms

  • Animals
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / metabolism*
  • Endothelin A Receptor Antagonists / pharmacology
  • Endothelin A Receptor Antagonists / therapeutic use
  • Endothelin-1 / metabolism
  • Humans
  • Kidney / drug effects
  • Kidney / metabolism
  • Receptor, Endothelin A / metabolism*

Substances

  • Endothelin A Receptor Antagonists
  • Endothelin-1
  • Receptor, Endothelin A