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NTCP deficiency in mice protects against obesity and hepatosteatosis
Bile acids play a major role in the regulation of lipid and energy metabolism. Here we propose the hepatic bile acid uptake transporter Na(+) taurocholate cotransporting polypeptide (NTCP) as a target to prolong postprandial bile acid elevations in plasma. Reducing hepatic clearance of bile acids fr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6675549/ https://www.ncbi.nlm.nih.gov/pubmed/31237863 http://dx.doi.org/10.1172/jci.insight.127197 |
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author | Donkers, Joanne M. Kooijman, Sander Slijepcevic, Davor Kunst, Roni F. Roscam Abbing, Reinout L.P. Haazen, Lizette de Waart, Dirk R. Levels, Johannes H.M. Schoonjans, Kristina Rensen, Patrick C.N. Oude Elferink, Ronald P.J. van de Graaf, Stan F.J. |
author_facet | Donkers, Joanne M. Kooijman, Sander Slijepcevic, Davor Kunst, Roni F. Roscam Abbing, Reinout L.P. Haazen, Lizette de Waart, Dirk R. Levels, Johannes H.M. Schoonjans, Kristina Rensen, Patrick C.N. Oude Elferink, Ronald P.J. van de Graaf, Stan F.J. |
author_sort | Donkers, Joanne M. |
collection | PubMed |
description | Bile acids play a major role in the regulation of lipid and energy metabolism. Here we propose the hepatic bile acid uptake transporter Na(+) taurocholate cotransporting polypeptide (NTCP) as a target to prolong postprandial bile acid elevations in plasma. Reducing hepatic clearance of bile acids from plasma by genetic deletion of NTCP moderately increased plasma bile acid levels, reduced diet-induced obesity, attenuated hepatic steatosis, and lowered plasma cholesterol levels. NTCP and G protein–coupled bile acid receptor–double KO (TGR5–double KO) mice were equally protected against diet-induced obesity as NTCP–single KO mice. NTCP-KO mice displayed decreased intestinal fat absorption and a trend toward higher fecal energy output. Furthermore, NTCP deficiency was associated with an increased uncoupled respiration in brown adipose tissue, leading to increased energy expenditure. We conclude that targeting NTCP-mediated bile acid uptake can be a novel approach to treat obesity and obesity-related hepatosteatosis by simultaneously dampening intestinal fat absorption and increasing energy expenditure. |
format | Online Article Text |
id | pubmed-6675549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-66755492019-08-13 NTCP deficiency in mice protects against obesity and hepatosteatosis Donkers, Joanne M. Kooijman, Sander Slijepcevic, Davor Kunst, Roni F. Roscam Abbing, Reinout L.P. Haazen, Lizette de Waart, Dirk R. Levels, Johannes H.M. Schoonjans, Kristina Rensen, Patrick C.N. Oude Elferink, Ronald P.J. van de Graaf, Stan F.J. JCI Insight Research Article Bile acids play a major role in the regulation of lipid and energy metabolism. Here we propose the hepatic bile acid uptake transporter Na(+) taurocholate cotransporting polypeptide (NTCP) as a target to prolong postprandial bile acid elevations in plasma. Reducing hepatic clearance of bile acids from plasma by genetic deletion of NTCP moderately increased plasma bile acid levels, reduced diet-induced obesity, attenuated hepatic steatosis, and lowered plasma cholesterol levels. NTCP and G protein–coupled bile acid receptor–double KO (TGR5–double KO) mice were equally protected against diet-induced obesity as NTCP–single KO mice. NTCP-KO mice displayed decreased intestinal fat absorption and a trend toward higher fecal energy output. Furthermore, NTCP deficiency was associated with an increased uncoupled respiration in brown adipose tissue, leading to increased energy expenditure. We conclude that targeting NTCP-mediated bile acid uptake can be a novel approach to treat obesity and obesity-related hepatosteatosis by simultaneously dampening intestinal fat absorption and increasing energy expenditure. American Society for Clinical Investigation 2019-07-25 /pmc/articles/PMC6675549/ /pubmed/31237863 http://dx.doi.org/10.1172/jci.insight.127197 Text en © 2019 Donkers et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Donkers, Joanne M. Kooijman, Sander Slijepcevic, Davor Kunst, Roni F. Roscam Abbing, Reinout L.P. Haazen, Lizette de Waart, Dirk R. Levels, Johannes H.M. Schoonjans, Kristina Rensen, Patrick C.N. Oude Elferink, Ronald P.J. van de Graaf, Stan F.J. NTCP deficiency in mice protects against obesity and hepatosteatosis |
title | NTCP deficiency in mice protects against obesity and hepatosteatosis |
title_full | NTCP deficiency in mice protects against obesity and hepatosteatosis |
title_fullStr | NTCP deficiency in mice protects against obesity and hepatosteatosis |
title_full_unstemmed | NTCP deficiency in mice protects against obesity and hepatosteatosis |
title_short | NTCP deficiency in mice protects against obesity and hepatosteatosis |
title_sort | ntcp deficiency in mice protects against obesity and hepatosteatosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6675549/ https://www.ncbi.nlm.nih.gov/pubmed/31237863 http://dx.doi.org/10.1172/jci.insight.127197 |
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