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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Main Authors: Marko Matic, Galyna Bryzgalova, Hui Gao, Per Antonson, Patricia Humire, Yoko Omoto, Neil Portwood, Camilla Pramfalk, Suad Efendic, Per-Olof Berggren, Jan-Åke Gustafsson, Karin Dahlman-Wright
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3581463?pdf=render
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spelling doaj-78c9ceb9069a42e8ae141228c6a116562020-11-25T02:31:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5745810.1371/journal.pone.0057458Estrogen signalling and the metabolic syndrome: targeting the hepatic estrogen receptor alpha action.Marko MaticGalyna BryzgalovaHui GaoPer AntonsonPatricia HumireYoko OmotoNeil PortwoodCamilla PramfalkSuad EfendicPer-Olof BerggrenJan-Åke GustafssonKarin Dahlman-WrightAn 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.http://europepmc.org/articles/PMC3581463?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marko Matic
Galyna Bryzgalova
Hui Gao
Per Antonson
Patricia Humire
Yoko Omoto
Neil Portwood
Camilla Pramfalk
Suad Efendic
Per-Olof Berggren
Jan-Åke Gustafsson
Karin Dahlman-Wright
spellingShingle Marko Matic
Galyna Bryzgalova
Hui Gao
Per Antonson
Patricia Humire
Yoko Omoto
Neil Portwood
Camilla Pramfalk
Suad Efendic
Per-Olof Berggren
Jan-Åke Gustafsson
Karin Dahlman-Wright
Estrogen signalling and the metabolic syndrome: targeting the hepatic estrogen receptor alpha action.
PLoS ONE
author_facet Marko Matic
Galyna Bryzgalova
Hui Gao
Per Antonson
Patricia Humire
Yoko Omoto
Neil Portwood
Camilla Pramfalk
Suad Efendic
Per-Olof Berggren
Jan-Åke Gustafsson
Karin Dahlman-Wright
author_sort Marko Matic
title 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_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_sort estrogen signalling and the metabolic syndrome: targeting the hepatic estrogen receptor alpha action.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
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.
url http://europepmc.org/articles/PMC3581463?pdf=render
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