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Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action

An increasing body of evidence now links estrogenic signalling with the metabolic syndrome (MS). Despite the beneficial estrogenic effects in reversing some of the MS symptoms, the underlying mechanisms remain largely undiscovered. We have previously shown that total estrogen receptor alpha (ERα) kn...

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Autores principales: Matic, Marko, Bryzgalova, Galyna, Gao, Hui, Antonson, Per, Humire, Patricia, Omoto, Yoko, Portwood, Neil, Pramfalk, Camilla, Efendic, Suad, Berggren, Per-Olof, Gustafsson, Jan-Åke, Dahlman-Wright, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581463/
https://www.ncbi.nlm.nih.gov/pubmed/23451233
http://dx.doi.org/10.1371/journal.pone.0057458
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author Matic, Marko
Bryzgalova, Galyna
Gao, Hui
Antonson, Per
Humire, Patricia
Omoto, Yoko
Portwood, Neil
Pramfalk, Camilla
Efendic, Suad
Berggren, Per-Olof
Gustafsson, Jan-Åke
Dahlman-Wright, Karin
author_facet Matic, Marko
Bryzgalova, Galyna
Gao, Hui
Antonson, Per
Humire, Patricia
Omoto, Yoko
Portwood, Neil
Pramfalk, Camilla
Efendic, Suad
Berggren, Per-Olof
Gustafsson, Jan-Åke
Dahlman-Wright, Karin
author_sort Matic, Marko
collection PubMed
description An increasing body of evidence now links estrogenic signalling with the metabolic syndrome (MS). Despite the beneficial estrogenic effects in reversing some of the MS symptoms, the underlying mechanisms remain largely undiscovered. We have previously shown that total estrogen receptor alpha (ERα) knockout (KO) mice exhibit hepatic insulin resistance. To determine whether liver-selective ablation of ERα recapitulates metabolic phenotypes of ERKO mice we generated a liver-selective ERαKO mouse model, LERKO. We demonstrate that LERKO mice have efficient reduction of ERα selectively within the liver. However, LERKO and wild type control mice do not differ in body weight, and have a comparable hormone profile as well as insulin and glucose response, even when challenged with a high fat diet. Furthermore, LERKO mice display very minor changes in their hepatic transcript profile. Collectively, our findings indicate that hepatic ERα action may not be the responsible factor for the previously identified hepatic insulin resistance in ERαKO mice.
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spelling pubmed-35814632013-02-28 Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action Matic, Marko Bryzgalova, Galyna Gao, Hui Antonson, Per Humire, Patricia Omoto, Yoko Portwood, Neil Pramfalk, Camilla Efendic, Suad Berggren, Per-Olof Gustafsson, Jan-Åke Dahlman-Wright, Karin PLoS One Research Article An increasing body of evidence now links estrogenic signalling with the metabolic syndrome (MS). Despite the beneficial estrogenic effects in reversing some of the MS symptoms, the underlying mechanisms remain largely undiscovered. We have previously shown that total estrogen receptor alpha (ERα) knockout (KO) mice exhibit hepatic insulin resistance. To determine whether liver-selective ablation of ERα recapitulates metabolic phenotypes of ERKO mice we generated a liver-selective ERαKO mouse model, LERKO. We demonstrate that LERKO mice have efficient reduction of ERα selectively within the liver. However, LERKO and wild type control mice do not differ in body weight, and have a comparable hormone profile as well as insulin and glucose response, even when challenged with a high fat diet. Furthermore, LERKO mice display very minor changes in their hepatic transcript profile. Collectively, our findings indicate that hepatic ERα action may not be the responsible factor for the previously identified hepatic insulin resistance in ERαKO mice. Public Library of Science 2013-02-25 /pmc/articles/PMC3581463/ /pubmed/23451233 http://dx.doi.org/10.1371/journal.pone.0057458 Text en © 2013 Matic et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Matic, Marko
Bryzgalova, Galyna
Gao, Hui
Antonson, Per
Humire, Patricia
Omoto, Yoko
Portwood, Neil
Pramfalk, Camilla
Efendic, Suad
Berggren, Per-Olof
Gustafsson, Jan-Åke
Dahlman-Wright, Karin
Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title_full Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title_fullStr Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title_full_unstemmed Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title_short Estrogen Signalling and the Metabolic Syndrome: Targeting the Hepatic Estrogen Receptor Alpha Action
title_sort estrogen signalling and the metabolic syndrome: targeting the hepatic estrogen receptor alpha action
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581463/
https://www.ncbi.nlm.nih.gov/pubmed/23451233
http://dx.doi.org/10.1371/journal.pone.0057458
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