ETA-receptor antagonists or allosteric modulators?

Jo G R De Mey, Matthijs G Compeer, Pieter Lemkens, Merlijn J P M T Meens

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

The paracrine signaling peptide endothelin-1 (ET1) is involved in cardiovascular diseases, cancer and chronic pain. It acts on class A G-protein-coupled receptors (GPCRs) but displays atypical pharmacology. It binds tightly to ET receptor type A (ET(A)) and causes long-lasting effects. In resistance arteries, the long-lasting contractile effects can only be partly and reversibly relaxed by low-molecular-weight ET(A) antagonists (ERAs). However, the neuropeptide calcitonin-gene-related peptide selectively terminates binding of ET1 to ET(A). We propose that ET1 binds polyvalently to ET(A) and that ERAs and the physiological antagonist allosterically reduce ET(A) functions. Combining the two-state model and the two-domain model of GPCR function and considering receptor activation beyond agonist binding might lead to better anti-endothelinergic drugs. Future studies could lead to compounds that discriminate between ET(A)-mediated effects of the endogenous isopeptides ET1, ET2 and ET3 and that become more effective when the activity of the endogenous endothelin system is elevated.

Original languageEnglish
JournalTrends in Pharmacological Sciences
Volume32
Issue number6
Pages (from-to)345-351
ISSN0165-6147
DOIs
Publication statusPublished - Jun 2011
Externally publishedYes

Keywords

  • Allosteric Regulation
  • Animals
  • Calcitonin Gene-Related Peptide
  • Cardiovascular Diseases
  • Chronic Disease
  • Endothelin A Receptor Antagonists
  • Endothelins
  • Humans
  • Models, Biological
  • Neoplasms
  • Pain
  • Protein Binding
  • Rats
  • Receptor, Endothelin A
  • Structure-Activity Relationship
  • Vasodilator Agents

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