Literature DB >> 25809182

β3 -AR and the vertebrate heart: a comparative view.

S Imbrogno1, A Gattuso1, R Mazza1, T Angelone1,2, M C Cerra1,2.   

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.
© 2015 Scandinavian Physiological Society. Published by John Wiley & Sons Ltd.

Entities:  

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

Mesh:

Substances:

Year:  2015        PMID: 25809182     DOI: 10.1111/apha.12493

Source DB:  PubMed          Journal:  Acta Physiol (Oxf)        ISSN: 1748-1708            Impact factor:   6.311


  5 in total

1.  Effects of epinephrine exposure on contractile performance of compact and spongy myocardium from rainbow trout (Oncorhynchus mykiss) during hypoxia.

Authors:  Jordan C Roberts; Douglas A Syme
Journal:  Fish Physiol Biochem       Date:  2017-08-09       Impact factor: 2.794

Review 2.  Targeting β3-Adrenergic Receptors in the Heart: Selective Agonism and β-Blockade.

Authors:  Alessandro Cannavo; Walter J Koch
Journal:  J Cardiovasc Pharmacol       Date:  2017-02       Impact factor: 3.105

Review 3.  The goldfish Carassius auratus: an emerging animal model for comparative cardiac research.

Authors:  Mariacristina Filice; Maria Carmela Cerra; Sandra Imbrogno
Journal:  J Comp Physiol B       Date:  2021-08-28       Impact factor: 2.200

4.  Shaping the cardiac response to hypoxia: NO and its partners in teleost fish.

Authors:  Sandra Imbrogno; Tiziano Verri; Mariacristina Filice; Amilcare Barca; Roberta Schiavone; Alfonsina Gattuso; Maria Carmela Cerra
Journal:  Curr Res Physiol       Date:  2022-04-04

5.  Regulation of heart rate following genetic deletion of the ß1 adrenergic receptor in larval zebrafish.

Authors:  William Joyce; Yihang K Pan; Kayla Garvey; Vishal Saxena; Steve F Perry
Journal:  Acta Physiol (Oxf)       Date:  2022-06-16       Impact factor: 7.523

  5 in total

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