微生物群
肠道微生物群
肠道菌群
生物
免疫学
生物信息学
作者
Johnson Lok,Congjia Chen,Valeria Iannone,Ambrin Farizah Babu,Emily Kwun Kwan Lo,Ruben Vazquez-Uribe,Troels Holger Vaaben,Mikko I. Kettunen,Otto Savolainen,Ursula Schwab,Morten Otto Alexander Sommer,Kati Hanhineva,Marjukka Kolehmainen,Hani El‐Nezami,Carlos Gómez-Gallego
标识
DOI:10.1021/acs.jafc.5c01674
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.
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