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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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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