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Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System

Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is protective against the development and progression of CVD. Although large-scale randomized trials of postmenopausal hormone replacement therapy faile...

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Autores principales: Ueda, Kazutaka, Adachi, Yusuke, Liu, Pangyen, Fukuma, Nobuaki, Takimoto, Eiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965027/
https://www.ncbi.nlm.nih.gov/pubmed/31998238
http://dx.doi.org/10.3389/fendo.2019.00909
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author Ueda, Kazutaka
Adachi, Yusuke
Liu, Pangyen
Fukuma, Nobuaki
Takimoto, Eiki
author_facet Ueda, Kazutaka
Adachi, Yusuke
Liu, Pangyen
Fukuma, Nobuaki
Takimoto, Eiki
author_sort Ueda, Kazutaka
collection PubMed
description Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is protective against the development and progression of CVD. Although large-scale randomized trials of postmenopausal hormone replacement therapy failed to show cardiovascular benefits, recent ELITE study demonstrated anti-atherosclerotic benefits of exogenous estrogen depending on the initiation timing of the therapy. These results have urged us to better understand the mechanisms for actions of estrogens on CVD. Here, we review experimental and human studies, highlighting the emerging role of estrogen's non-nuclear actions linking to NO-cGMP signaling pathways.
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spelling pubmed-69650272020-01-29 Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System Ueda, Kazutaka Adachi, Yusuke Liu, Pangyen Fukuma, Nobuaki Takimoto, Eiki Front Endocrinol (Lausanne) Endocrinology Premenopausal females have a lower incidence of death from cardiovascular disease (CVD) than male counterparts, supporting the notion that estrogen is protective against the development and progression of CVD. Although large-scale randomized trials of postmenopausal hormone replacement therapy failed to show cardiovascular benefits, recent ELITE study demonstrated anti-atherosclerotic benefits of exogenous estrogen depending on the initiation timing of the therapy. These results have urged us to better understand the mechanisms for actions of estrogens on CVD. Here, we review experimental and human studies, highlighting the emerging role of estrogen's non-nuclear actions linking to NO-cGMP signaling pathways. Frontiers Media S.A. 2020-01-10 /pmc/articles/PMC6965027/ /pubmed/31998238 http://dx.doi.org/10.3389/fendo.2019.00909 Text en Copyright © 2020 Ueda, Adachi, Liu, Fukuma and Takimoto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Ueda, Kazutaka
Adachi, Yusuke
Liu, Pangyen
Fukuma, Nobuaki
Takimoto, Eiki
Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title_full Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title_fullStr Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title_full_unstemmed Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title_short Regulatory Actions of Estrogen Receptor Signaling in the Cardiovascular System
title_sort regulatory actions of estrogen receptor signaling in the cardiovascular system
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965027/
https://www.ncbi.nlm.nih.gov/pubmed/31998238
http://dx.doi.org/10.3389/fendo.2019.00909
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