Lok Johnson, Chen Congjia, Iannone Valeria, Babu Ambrin Farizah, Lo Emily Kwun Kwan, Vazquez-Uribe Ruben, Vaaben Troels Holger, Kettunen Mikko, Savolainen Otto, Schwab Ursula, Sommer Morten Otto Alexander, Hanhineva Kati, Kolehmainen Marjukka, El-Nezami Hani, Gómez-Gallego Carlos
School of Medicine, Institute of Public Health and Clinical Nutrition, University of Eastern Finland, Kuopio 70210, Finland.
School of Biological Sciences, University of Hong Kong, Pokfulam, Hong Kong SAR 999077, China.
J Agric Food Chem. 2025 Jun 18;73(24):15199-15214. doi: 10.1021/acs.jafc.5c01674. Epub 2025 Jun 6.
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 Nissle 1917 expressing IGF1 (EcNI) or aldafermin (EcNA), and control groups received 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.
肠道微生物群失调和内分泌失调是代谢功能障碍相关脂肪性肝病(MASLD)发展的关键因素。本研究评估了先进的微生物组疗法能否在MASLD恢复过程中恢复肠道微生物平衡和肠-肝轴平衡。使用高脂肪、高糖饮食诱导小鼠发生MASLD,然后改为标准饮食,干预组接受表达IGF1的工程化1917株大肠杆菌(EcNI)或艾达费明(EcNA),对照组接受1917株大肠杆菌载体(EcN)或不进行微生物干预(CTRL)。与对照组相比,EcNI和EcNA通过降低肝脏脂肪、血浆胆固醇和体重,同时增加细菌多样性、血浆乙酸盐和丙酸盐,并调节特定微生物群,潜在地缓解了失调,从而改善了MASLD的恢复。此外,EcNI和EcNA下调了乙酰辅酶A、类固醇激素生物合成途径,EcNA上调了磷酸戊糖途径和丙酮酸,这与氧化应激降低有关。这些结果表明,EcNI和EcNA是MASLD潜在的新型治疗方法。