Advanced Microbiome Therapeutics Accelerate MASLD Recovery by Restoring Intestinal Microbiota Equilibrium and the Gut-Liver Axis in a Mouse Model

被引:0
作者
Lok, Johnson [1 ]
Chen, Congjia [2 ]
Iannone, Valeria [1 ]
Babu, Ambrin Farizah [1 ,3 ]
Lo, Emily Kwun Kwan [2 ]
Vazquez-Uribe, Ruben [4 ,5 ]
Vaaben, Troels Holger [4 ]
Kettunen, Mikko [6 ]
Savolainen, Otto [1 ,7 ]
Schwab, Ursula [1 ,8 ]
Sommer, Morten Otto Alexander [4 ]
Hanhineva, Kati [1 ,3 ,9 ]
Kolehmainen, Marjukka [1 ]
El-Nezami, Hani [1 ,2 ]
Gomez-Gallego, Carlos [1 ]
机构
[1] Univ Eastern Finland, Inst Publ Hlth & Clin Nutr, Sch Med, Kuopio 70210, Finland
[2] Univ Hong Kong, Sch Biol Sci, Pokfulam, Hong Kong 999077, Peoples R China
[3] Afekta Technol Ltd, Kuopio 70210, Finland
[4] Tech Univ Denmark, Novo Nordisk Fdn, Ctr Biosustainabil, DK-2800 Lyngby, Denmark
[5] Vlaams Inst Biotechnol, Ctr Microbiol, B-3001 Leuven, Belgium
[6] Univ Eastern Finland, AI Virtanen Inst Mol Sci, Biomed Imaging Unit, Kuopio 70211, Finland
[7] Chalmers Univ Technol, Dept Life Sci, Chalmers Mass Spectrometry Infrastruct, SE-41296 Gothenburg, Sweden
[8] Kuopio Univ Hosp, Dept Med Endocrinol & Clin Nutr, Wellbeing Serv Cty North Savo, Kuopio 70210, Finland
[9] Univ Turku, Dept Life Technol, Food Sci Unit, Turku 20014, Finland
基金
芬兰科学院;
关键词
nonalcoholic fattyliver disease (NAFLD); E. coli Nissle1917; insulin-like growth factor 1; fibroblast growthfactor 19; aldafermin; integrative multiomics; GROWTH-FACTOR-I; OXIDATIVE STRESS; WEIGHT-LOSS; DISEASE; LIPOGENESIS; DYSBIOSIS; PYRUVATE; STEATOHEPATITIS; MAINTENANCE; RESOLUTION;
D O I
10.1021/acs.jafc.5c01674
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Gut microbiota dysbiosis and endocrine dysregulation are key players in metabolic dysfunction-associated steatotic liver disease (MASLD) development. This study evaluated whether advanced microbiome therapeutics can restore intestinal microbial equilibrium and gut-liver axis balance during MASLD recovery. MASLD was induced in mice using a high-fat, high-sugar diet, and then shifted to a standard diet, where intervention groups received engineered Escherichia coli Nissle 1917 expressing IGF1 (EcNI) or aldafermin (EcNA), and control groups received E. coli Nissle 1917 vehicle (EcN) or no microbial intervention (CTRL). EcNI and EcNA improved MASLD recovery compared to controls by lowering hepatic fat, plasma cholesterol, and body weight, while increasing bacterial diversity, plasma acetate, and propionate, and modulating particular microbial groups, potentially alleviating dysbiosis. Additionally, EcNI and EcNA downregulated acetyl-CoA, the steroid hormone biosynthesis pathway, and EcNA upregulated the pentose phosphate pathway and pyruvate, which are related to oxidative stress reduction. These results suggest that EcNI and EcNA are potential novel treatments for MASLD.
引用
收藏
页码:15199 / 15214
页数:16
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