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An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity

Alpha-1 adrenergic receptors (α1-ARs) play adaptive and protective roles in the heart. Dabuzalgron is an oral selective α1A-AR agonist that was well tolerated in multiple clinical trials of treatment for urinary incontinence, but has never been used to treat heart disease in humans or animal models....

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Autores principales: Beak, Ju Youn, Huang, Wei, Parker, Joel S., Hicks, Sean T., Patterson, Cam, Simpson, Paul C., Ma, Anqi, Jin, Jian, Jensen, Brian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343290/
https://www.ncbi.nlm.nih.gov/pubmed/28286875
http://dx.doi.org/10.1016/j.jacbts.2016.10.006
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author Beak, Ju Youn
Huang, Wei
Parker, Joel S.
Hicks, Sean T.
Patterson, Cam
Simpson, Paul C.
Ma, Anqi
Jin, Jian
Jensen, Brian C.
author_facet Beak, Ju Youn
Huang, Wei
Parker, Joel S.
Hicks, Sean T.
Patterson, Cam
Simpson, Paul C.
Ma, Anqi
Jin, Jian
Jensen, Brian C.
author_sort Beak, Ju Youn
collection PubMed
description Alpha-1 adrenergic receptors (α1-ARs) play adaptive and protective roles in the heart. Dabuzalgron is an oral selective α1A-AR agonist that was well tolerated in multiple clinical trials of treatment for urinary incontinence, but has never been used to treat heart disease in humans or animal models. In this study, the authors administered dabuzalgron to mice treated with doxorubicin (DOX), a widely used chemotherapeutic agent with dose-limiting cardiotoxicity that can lead to heart failure (HF). Dabuzalgron protected against DOX-induced cardiotoxicity, likely by preserving mitochondrial function. These results suggest that activating cardiac α1A-ARs with dabuzalgron, a well-tolerated oral agent, might represent a novel approach to treating HF.
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spelling pubmed-53432902017-10-20 An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity Beak, Ju Youn Huang, Wei Parker, Joel S. Hicks, Sean T. Patterson, Cam Simpson, Paul C. Ma, Anqi Jin, Jian Jensen, Brian C. JACC Basic Transl Sci PRECLINICAL RESEARCH Alpha-1 adrenergic receptors (α1-ARs) play adaptive and protective roles in the heart. Dabuzalgron is an oral selective α1A-AR agonist that was well tolerated in multiple clinical trials of treatment for urinary incontinence, but has never been used to treat heart disease in humans or animal models. In this study, the authors administered dabuzalgron to mice treated with doxorubicin (DOX), a widely used chemotherapeutic agent with dose-limiting cardiotoxicity that can lead to heart failure (HF). Dabuzalgron protected against DOX-induced cardiotoxicity, likely by preserving mitochondrial function. These results suggest that activating cardiac α1A-ARs with dabuzalgron, a well-tolerated oral agent, might represent a novel approach to treating HF. Elsevier 2017-02-27 /pmc/articles/PMC5343290/ /pubmed/28286875 http://dx.doi.org/10.1016/j.jacbts.2016.10.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle PRECLINICAL RESEARCH
Beak, Ju Youn
Huang, Wei
Parker, Joel S.
Hicks, Sean T.
Patterson, Cam
Simpson, Paul C.
Ma, Anqi
Jin, Jian
Jensen, Brian C.
An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title_full An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title_fullStr An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title_full_unstemmed An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title_short An Oral Selective Alpha-1A Adrenergic Receptor Agonist Prevents Doxorubicin Cardiotoxicity
title_sort oral selective alpha-1a adrenergic receptor agonist prevents doxorubicin cardiotoxicity
topic PRECLINICAL RESEARCH
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343290/
https://www.ncbi.nlm.nih.gov/pubmed/28286875
http://dx.doi.org/10.1016/j.jacbts.2016.10.006
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