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dc.contributor.author
Makki, Kassem
dc.contributor.author
Brolin, Harald
dc.contributor.author
Petersen, Natalia
dc.contributor.author
Henricsson, Marcus
dc.contributor.author
Christensen, Dan Ploug
dc.contributor.author
Khan, Muhammad Tanweer
dc.contributor.author
Wahlström, Annika
dc.contributor.author
Bergh, Per-Olof
dc.contributor.author
Tremaroli, Valentina
dc.contributor.author
Schoonjans, Kristina
dc.contributor.author
Marschall, Hanns-Ulrich
dc.contributor.author
Bäckhed, Fredrik
dc.date.accessioned
2023-03-09T08:45:14Z
dc.date.available
2022-06-22T04:34:41Z
dc.date.available
2022-06-22T14:15:41Z
dc.date.available
2023-03-09T08:45:14Z
dc.date.issued
2023-02
dc.identifier.issn
1468-3288
dc.identifier.issn
0017-5749
dc.identifier.other
10.1136/gutjnl-2021-326541
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/553802
dc.identifier.doi
10.3929/ethz-b-000553802
dc.description.abstract
Objective Dietary fibres are essential for maintaining microbial diversity and the gut microbiota can modulate host physiology by metabolising the fibres. Here, we investigated whether the soluble dietary fibre oligofructose improves host metabolism by modulating bacterial transformation of secondary bile acids in mice fed western-style diet. Design To assess the impact of dietary fibre supplementation on bile acid transformation by gut bacteria, we fed conventional wild-type and TGR5 knockout mice western-style diet enriched or not with cellulose or oligofructose. In addition, we used germ-free mice and in vitro cultures to evaluate the activity of bacteria to transform bile acids in the caecal content of mice fed with western-style diet enriched with oligofructose. Finally, we treated wild-type and TGR5 knockout mice orally with hyodeoxycholic acid to assess its antidiabetic effects. Results We show that oligofructose sustains the production of 6α-hydroxylated bile acids from primary bile acids by gut bacteria when fed western-style diet. Mechanistically, we demonstrated that the effects of oligofructose on 6α-hydroxylated bile acids were microbiota dependent and specifically required functional TGR5 signalling to reduce body weight gain and improve glucose metabolism. Furthermore, we show that the 6α-hydroxylated bile acid hyodeoxycholic acid stimulates TGR5 signalling, in vitro and in vivo, and increases GLP-1R activity to improve host glucose metabolism. Conclusion Modulation of the gut microbiota with oligofructose enriches bacteria involved in 6α-hydroxylated bile acid production and leads to TGR5-GLP1R axis activation to improve body weight and metabolism under western-style diet feeding in mice.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
BMJ
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.title
6α-hydroxylated bile acids mediate TGR5 signalling to improve glucose metabolism upon dietary fiber supplementation in mice
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2022-06-13
ethz.journal.title
Gut
ethz.journal.volume
72
en_US
ethz.journal.issue
2
en_US
ethz.pages.start
314
en_US
ethz.pages.end
324
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.date.deposited
2022-06-22T04:35:13Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2023-03-09T08:45:16Z
ethz.rosetta.lastUpdated
2024-02-02T20:49:06Z
ethz.rosetta.versionExported
true
ethz.COinS
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