Current and future strategies for targeting the endothelin pathway in cardiovascular disease

Nat Cardiovasc Res. 2023 Nov;2(11):972-990. doi: 10.1038/s44161-023-00347-2. Epub 2023 Nov 2.

Abstract

The first endothelin (ET)-1 receptor antagonist was approved for clinical use over 20 years ago, but to date this class of compounds has been limited to treating pulmonary arterial hypertension, a rare disease. Translational research over the last 5 years has reignited interest in the ET system as a therapeutic target across the spectrum of cardiovascular diseases including resistant hypertension, microvascular angina and post-coronavirus disease 2019 conditions. Notable developments include approval of a new ETA receptor antagonist and, intriguingly, combining the actions of ETA and an angiotensin II type 1 receptor antagonist within the same novel small molecule. Combinations of ET receptor blockers with other drugs, including phosphodiesterase-5 inhibitors and sodium-glucose co-transporter-2 antagonists, may drive synergistic benefits with the prospect of alleviating side effects. These new therapeutic strategies have the potential to dramatically widen the scope of indications targeting the ET-1 pathway.

Publication types

  • Review

MeSH terms

  • Animals
  • COVID-19
  • Cardiovascular Diseases* / drug therapy
  • Cardiovascular Diseases* / metabolism
  • Endothelin Receptor Antagonists* / pharmacology
  • Endothelin Receptor Antagonists* / therapeutic use
  • Endothelin-1 / antagonists & inhibitors
  • Endothelin-1 / metabolism
  • Endothelins / metabolism
  • Humans
  • SARS-CoV-2 / drug effects
  • Signal Transduction / drug effects

Substances

  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Endothelins