β3 -AR and the vertebrate heart: a comparative view

Acta Physiol (Oxf). 2015 Jun;214(2):158-75. doi: 10.1111/apha.12493. Epub 2015 Apr 6.

Abstract

Recent cardiovascular research showed that, together with β1- and β2-adrenergic receptors (ARs), β3-ARs contribute to the catecholamine (CA)-dependent control of the heart. β3-ARs structure, function and ligands were investigated in mammals because of their applicative potential in human cardiovascular diseases. Only recently, the concept of a β3-AR-dependent cardiac modulation was extended to non-mammalian vertebrates, although information is still scarce and fragmentary. β3-ARs were structurally described in fish, showing a closer relationship to mammalian β1-AR than β2-AR. Functional β3-ARs are present in the cardiac tissue of teleosts and amphibians. As in mammals, activation of these receptors elicits a negative modulation of the inotropic performance through the involvement of the endothelium endocardium (EE), Gi/0 proteins and the nitric oxide (NO) signalling. This review aims to comparatively analyse data from literature on β3-ARs in mammals, with those on teleosts and amphibians. The purpose is to highlight aspects of uniformity and diversity of β3-ARs structure, ligands activity, function and signalling cascades throughout vertebrates. This may provide new perspectives aimed to clarify the biological relevance of β3-ARs in the context of the nervous and humoral control of the heart and its functional plasticity.

Keywords: adrenergic receptors; amphibians; cardiac performance; mammals; nitric oxide; teleosts.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Heart / physiology*
  • Humans
  • Nitric Oxide / metabolism*
  • Receptors, Adrenergic, beta-3 / metabolism*
  • Signal Transduction / physiology*
  • Vertebrates / metabolism*

Substances

  • Adrenergic beta-Agonists
  • Receptors, Adrenergic, beta-3
  • Nitric Oxide