Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model
Background: Gut microbiota dysbiosis is associated with the development of non‑alcoholic steatohepatitis (NASH) through modulation of gut barrier, inflammation, lipid metabolism, bile acid signaling and short‑chain fatty acid production. The aim of this study was to describe the impact of a choline‑...
Main Authors: | , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Springer Science and Business Media LLC
2022
|
Subjects: | |
Online Access: | http://umpir.ump.edu.my/id/eprint/38074/1/minipig.pdf |
_version_ | 1825815045818286080 |
---|---|
author | Ditte Olsen, Lützhøft Tim, Sinioja Berit Ø., Christoffersen Jakobsen, Rasmus Riemer Dawei, Geng Hajar Fauzan, Ahmad Ellen Marie, Straarup Karen-Margrethe, Pedersen Kot, Witold Henrik Duelund, Pedersen Susanna, Cirera Tuulia, Hyötyläinen Dennis Sandris, Nielsen Axel Kornerup, Hansen |
author_facet | Ditte Olsen, Lützhøft Tim, Sinioja Berit Ø., Christoffersen Jakobsen, Rasmus Riemer Dawei, Geng Hajar Fauzan, Ahmad Ellen Marie, Straarup Karen-Margrethe, Pedersen Kot, Witold Henrik Duelund, Pedersen Susanna, Cirera Tuulia, Hyötyläinen Dennis Sandris, Nielsen Axel Kornerup, Hansen |
author_sort | Ditte Olsen, Lützhøft |
collection | UMP |
description | Background: Gut microbiota dysbiosis is associated with the development of non‑alcoholic steatohepatitis (NASH) through modulation of gut barrier, inflammation, lipid metabolism, bile acid signaling and short‑chain fatty acid production. The aim of this study was to describe the impact of a choline‑deficient amino acid defined high fat diet (CDAHFD) on the gut microbiota in a male Göttingen Minipig model and on selected pathways implicated in the development of NASH. Results: Eight weeks of CDAHFD resulted in a significantly altered colon microbiota mainly driven by the bacterial families Lachnospiraceae and Enterobacteriaceae, being decreased and increased in relative abundance, respectively. Metabolomics analysis revealed that CDAHFD decreased colon content of short‑chain fatty acid and increased colonic pH. In addition, serum levels of the microbially produced metabolite imidazole propionate were significantly elevated as a consequence of CDAHFD feeding. Hepatic gene expression analysis showed upregulation of mechanistic target of rapamycin (mTOR) and Ras Homolog, MTORC1 binding in addition to downregulation of insulin receptor substrate 1, insulin receptor substrate 2 and the glucagon receptor in CDAHFD fed minipigs. Further, the consequences of CDAHFD feeding were associated with increased levels of circulating cholesterol, bile acids, and glucagon but not total amino acids. Conclusions: Our results indicate imidazole propionate as a new potentially relevant factor in relation to NASH and discuss the possible implication of gut microbiota dysbiosis in the development of NASH. In addition, the study emphasizes the need for considering the gut microbiota and its products when developing translational animal models for NASH. |
first_indexed | 2024-03-06T13:07:36Z |
format | Article |
id | UMPir38074 |
institution | Universiti Malaysia Pahang |
language | English |
last_indexed | 2024-03-06T13:07:36Z |
publishDate | 2022 |
publisher | Springer Science and Business Media LLC |
record_format | dspace |
spelling | UMPir380742023-07-27T02:54:18Z http://umpir.ump.edu.my/id/eprint/38074/ Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model Ditte Olsen, Lützhøft Tim, Sinioja Berit Ø., Christoffersen Jakobsen, Rasmus Riemer Dawei, Geng Hajar Fauzan, Ahmad Ellen Marie, Straarup Karen-Margrethe, Pedersen Kot, Witold Henrik Duelund, Pedersen Susanna, Cirera Tuulia, Hyötyläinen Dennis Sandris, Nielsen Axel Kornerup, Hansen HD Industries. Land use. Labor Q Science (General) Background: Gut microbiota dysbiosis is associated with the development of non‑alcoholic steatohepatitis (NASH) through modulation of gut barrier, inflammation, lipid metabolism, bile acid signaling and short‑chain fatty acid production. The aim of this study was to describe the impact of a choline‑deficient amino acid defined high fat diet (CDAHFD) on the gut microbiota in a male Göttingen Minipig model and on selected pathways implicated in the development of NASH. Results: Eight weeks of CDAHFD resulted in a significantly altered colon microbiota mainly driven by the bacterial families Lachnospiraceae and Enterobacteriaceae, being decreased and increased in relative abundance, respectively. Metabolomics analysis revealed that CDAHFD decreased colon content of short‑chain fatty acid and increased colonic pH. In addition, serum levels of the microbially produced metabolite imidazole propionate were significantly elevated as a consequence of CDAHFD feeding. Hepatic gene expression analysis showed upregulation of mechanistic target of rapamycin (mTOR) and Ras Homolog, MTORC1 binding in addition to downregulation of insulin receptor substrate 1, insulin receptor substrate 2 and the glucagon receptor in CDAHFD fed minipigs. Further, the consequences of CDAHFD feeding were associated with increased levels of circulating cholesterol, bile acids, and glucagon but not total amino acids. Conclusions: Our results indicate imidazole propionate as a new potentially relevant factor in relation to NASH and discuss the possible implication of gut microbiota dysbiosis in the development of NASH. In addition, the study emphasizes the need for considering the gut microbiota and its products when developing translational animal models for NASH. Springer Science and Business Media LLC 2022-12 Article PeerReviewed pdf en cc_by_4 http://umpir.ump.edu.my/id/eprint/38074/1/minipig.pdf Ditte Olsen, Lützhøft and Tim, Sinioja and Berit Ø., Christoffersen and Jakobsen, Rasmus Riemer and Dawei, Geng and Hajar Fauzan, Ahmad and Ellen Marie, Straarup and Karen-Margrethe, Pedersen and Kot, Witold and Henrik Duelund, Pedersen and Susanna, Cirera and Tuulia, Hyötyläinen and Dennis Sandris, Nielsen and Axel Kornerup, Hansen (2022) Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model. BMC Microbiology, 22 (287). pp. 1-14. ISSN 14712180. (Published) https://doi.org/10.1186%2Fs12866-022-02704-w 10.1186%2Fs12866-022-02704-w |
spellingShingle | HD Industries. Land use. Labor Q Science (General) Ditte Olsen, Lützhøft Tim, Sinioja Berit Ø., Christoffersen Jakobsen, Rasmus Riemer Dawei, Geng Hajar Fauzan, Ahmad Ellen Marie, Straarup Karen-Margrethe, Pedersen Kot, Witold Henrik Duelund, Pedersen Susanna, Cirera Tuulia, Hyötyläinen Dennis Sandris, Nielsen Axel Kornerup, Hansen Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title | Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title_full | Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title_fullStr | Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title_full_unstemmed | Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title_short | Marked gut microbiota dysbiosis and increased imidazole propionate are associated with a NASH Göttingen Minipig model |
title_sort | marked gut microbiota dysbiosis and increased imidazole propionate are associated with a nash gottingen minipig model |
topic | HD Industries. Land use. Labor Q Science (General) |
url | http://umpir.ump.edu.my/id/eprint/38074/1/minipig.pdf |
work_keys_str_mv | AT ditteolsenlutzhøft markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT timsinioja markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT beritøchristoffersen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT jakobsenrasmusriemer markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT daweigeng markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT hajarfauzanahmad markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT ellenmariestraarup markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT karenmargrethepedersen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT kotwitold markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT henrikduelundpedersen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT susannacirera markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT tuuliahyotylainen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT dennissandrisnielsen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel AT axelkorneruphansen markedgutmicrobiotadysbiosisandincreasedimidazolepropionateareassociatedwithanashgottingenminipigmodel |