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Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)

The beta-3 adrenergic receptor (β(3)-AR) is by far the least studied isotype of the beta-adrenergic sub-family. Despite its study being long hampered by the lack of suitable animal and cellular models and inter-species differences, a substantial body of literature on the subject has built up in the...

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Detalles Bibliográficos
Autores principales: Schena, Giorgia, Caplan, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523418/
https://www.ncbi.nlm.nih.gov/pubmed/30995798
http://dx.doi.org/10.3390/cells8040357
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author Schena, Giorgia
Caplan, Michael J.
author_facet Schena, Giorgia
Caplan, Michael J.
author_sort Schena, Giorgia
collection PubMed
description The beta-3 adrenergic receptor (β(3)-AR) is by far the least studied isotype of the beta-adrenergic sub-family. Despite its study being long hampered by the lack of suitable animal and cellular models and inter-species differences, a substantial body of literature on the subject has built up in the last three decades and the physiology of β(3)-AR is unraveling quickly. As will become evident in this work, β(3)-AR is emerging as an appealing target for novel pharmacological approaches in several clinical areas involving metabolic, cardiovascular, urinary, and ocular disease. In this review, we will discuss the most recent advances regarding β(3)-AR signaling and function and summarize how these findings translate, or may do so, into current clinical practice highlighting β(3)-AR’s great potential as a novel therapeutic target in a wide range of human conditions.
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spelling pubmed-65234182019-06-03 Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask) Schena, Giorgia Caplan, Michael J. Cells Review The beta-3 adrenergic receptor (β(3)-AR) is by far the least studied isotype of the beta-adrenergic sub-family. Despite its study being long hampered by the lack of suitable animal and cellular models and inter-species differences, a substantial body of literature on the subject has built up in the last three decades and the physiology of β(3)-AR is unraveling quickly. As will become evident in this work, β(3)-AR is emerging as an appealing target for novel pharmacological approaches in several clinical areas involving metabolic, cardiovascular, urinary, and ocular disease. In this review, we will discuss the most recent advances regarding β(3)-AR signaling and function and summarize how these findings translate, or may do so, into current clinical practice highlighting β(3)-AR’s great potential as a novel therapeutic target in a wide range of human conditions. MDPI 2019-04-16 /pmc/articles/PMC6523418/ /pubmed/30995798 http://dx.doi.org/10.3390/cells8040357 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Schena, Giorgia
Caplan, Michael J.
Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title_full Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title_fullStr Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title_full_unstemmed Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title_short Everything You Always Wanted to Know about β(3)-AR * (* But Were Afraid to Ask)
title_sort everything you always wanted to know about β(3)-ar * (* but were afraid to ask)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523418/
https://www.ncbi.nlm.nih.gov/pubmed/30995798
http://dx.doi.org/10.3390/cells8040357
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