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Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice
BACKGROUND: Obesity, non-alcoholic fatty liver disease (NAFLD) and its more advanced form non-alcoholic steatohepatitis (NASH) are important causes of morbidity and mortality worldwide. Bile acid dysregulation is a pivotal part in their pathogenesis. The aim of this study was to evaluate the bile ac...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013343/ https://www.ncbi.nlm.nih.gov/pubmed/35075592 http://dx.doi.org/10.1007/s12072-022-10296-w |
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author | Hartmann, Phillipp Duan, Yi Miyamoto, Yukiko Demir, Münevver Lang, Sonja Hasa, Elda Stern, Patrick Yamashita, Dennis Conrad, Mary Eckmann, Lars Schnabl, Bernd |
author_facet | Hartmann, Phillipp Duan, Yi Miyamoto, Yukiko Demir, Münevver Lang, Sonja Hasa, Elda Stern, Patrick Yamashita, Dennis Conrad, Mary Eckmann, Lars Schnabl, Bernd |
author_sort | Hartmann, Phillipp |
collection | PubMed |
description | BACKGROUND: Obesity, non-alcoholic fatty liver disease (NAFLD) and its more advanced form non-alcoholic steatohepatitis (NASH) are important causes of morbidity and mortality worldwide. Bile acid dysregulation is a pivotal part in their pathogenesis. The aim of this study was to evaluate the bile acid sequestrant colesevelam in a microbiome-humanized mouse model of diet-induced obesity and steatohepatitis. METHODS: Germ-free C57BL/6 mice were associated with stool from patients with NASH and subjected to 20 weeks of Western diet feeding with and without colesevelam. RESULTS: Colesevelam reduced Western diet-induced body and liver weight gain in microbiome-humanized mice compared with controls. It ameliorated Western diet-induced hepatic inflammation, steatosis, fibrosis and insulin resistance. Colesevelam increased de novo bile acid synthesis and decreased hepatic cholesterol content in microbiome-humanized mice fed a Western diet. It further induced the gene expression of the antimicrobials Reg3g and Reg3b in the distal small intestine and decreased plasma levels of LPS. CONCLUSIONS: Colesevelam ameliorates Western diet-induced steatohepatitis and obesity in microbiome-humanized mice. |
format | Online Article Text |
id | pubmed-9013343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-90133432022-05-02 Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice Hartmann, Phillipp Duan, Yi Miyamoto, Yukiko Demir, Münevver Lang, Sonja Hasa, Elda Stern, Patrick Yamashita, Dennis Conrad, Mary Eckmann, Lars Schnabl, Bernd Hepatol Int Original Article BACKGROUND: Obesity, non-alcoholic fatty liver disease (NAFLD) and its more advanced form non-alcoholic steatohepatitis (NASH) are important causes of morbidity and mortality worldwide. Bile acid dysregulation is a pivotal part in their pathogenesis. The aim of this study was to evaluate the bile acid sequestrant colesevelam in a microbiome-humanized mouse model of diet-induced obesity and steatohepatitis. METHODS: Germ-free C57BL/6 mice were associated with stool from patients with NASH and subjected to 20 weeks of Western diet feeding with and without colesevelam. RESULTS: Colesevelam reduced Western diet-induced body and liver weight gain in microbiome-humanized mice compared with controls. It ameliorated Western diet-induced hepatic inflammation, steatosis, fibrosis and insulin resistance. Colesevelam increased de novo bile acid synthesis and decreased hepatic cholesterol content in microbiome-humanized mice fed a Western diet. It further induced the gene expression of the antimicrobials Reg3g and Reg3b in the distal small intestine and decreased plasma levels of LPS. CONCLUSIONS: Colesevelam ameliorates Western diet-induced steatohepatitis and obesity in microbiome-humanized mice. Springer India 2022-01-24 /pmc/articles/PMC9013343/ /pubmed/35075592 http://dx.doi.org/10.1007/s12072-022-10296-w Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Hartmann, Phillipp Duan, Yi Miyamoto, Yukiko Demir, Münevver Lang, Sonja Hasa, Elda Stern, Patrick Yamashita, Dennis Conrad, Mary Eckmann, Lars Schnabl, Bernd Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title | Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title_full | Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title_fullStr | Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title_full_unstemmed | Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title_short | Colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
title_sort | colesevelam ameliorates non-alcoholic steatohepatitis and obesity in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013343/ https://www.ncbi.nlm.nih.gov/pubmed/35075592 http://dx.doi.org/10.1007/s12072-022-10296-w |
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