Probiotic Mixture Ameliorates a Diet-Induced MASLD/MASH Murine Model through the Regulation of Hepatic Lipid Metabolism and the Gut Microbiome

被引:6
|
作者
Zhang, Fangfei [1 ]
Lo, Emily Kwun Kwan [1 ]
Chen, Jiarui [2 ,3 ,4 ]
Wang, Ke [5 ,6 ]
Ismaiah, Marsena Jasiel [1 ]
Leung, Hoi Kit Matthew [1 ]
Zhao, Danyue [5 ,6 ]
Lee, Jetty Chung-Yung [1 ]
El-Nezami, Hani [1 ,7 ]
机构
[1] Univ Hong Kong, Sch Biol Sci, Hong Kong 000, Peoples R China
[2] Univ Hong Kong, State Key Lab Pharmaceut Biotechnol, Hong Kong 000, Peoples R China
[3] Univ Hong Kong, Dept Med, Hong Kong 000, Peoples R China
[4] Hans Knoll Inst Microbiome Dynam, Leibniz Inst Nat Prod Res & Infect Biol, D-07745 Jena, Germany
[5] Hong Kong Polytech Univ, Dept Food Sci & Nutr, Hong Kong 000, Peoples R China
[6] Hong Kong Polytech Univ, Res Inst Future Food, Hong Kong 000, Peoples R China
[7] Univ Eastern Finland, Sch Med, Inst Publ Hlth & Clin Nutr, FI-70211 Kuopio, Finland
关键词
metabolic dysfunction-associated steatotic liver disease; probiotic; gut microbiota; short-chain fatty acid; bile acid; BILE-ACID SYNTHESIS; CHAIN FATTY-ACIDS; DUBOSIELLA-NEWYORKENSIS; FIBROSIS PROGRESSION; INDUCED OBESITY; INFLAMMATION; ACCUMULATION; STEATOSIS; COLITIS; PATHWAY;
D O I
10.1021/acs.jafc.3c08910
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent metabolic disease that has no effective treatment. Our proprietary probiotic mixture, Prohep, has been proven in a previous study to be helpful in reducing hepatocellular carcinoma (HCC) in vivo. However, its prospective benefits on the treatment of other liver diseases such as MASLD, which is one of the major risk factors in the development of HCC, are unclear. To investigate the potential of Prohep in modulating the development and progression of MASLD, we first explored the effect of Prohep supplementation via voluntary intake in a high-fat diet (HFD)-induced MASLD/metabolic dysfunction-associated steatohepatitis (MASH) murine model. Our results indicated that Prohep alleviated HFD-induced liver steatosis and reduced excessive hepatic lipid accumulation and improved the plasma lipid profile when compared with HFD-fed control mice through suppressing hepatic de novo lipogenesis and cholesterol biosynthesis gene expressions. In addition, Prohep was able to modulate the gut microbiome, modify the bile acid (BA) profile, and elevate fecal short-chain fatty acid (SCFA) levels. Next, in a prolonged HFD-feeding MASLD/MASH model, we observed the effectiveness of Prohep in preventing the transition from MASLD to MASH via amelioration in hepatic steatosis, inflammation, and fibrosis. Taken together, Prohep could ameliorate HFD-induced MASLD and control the MASLD-to-MASH progression in mice. Our findings provide distinctive insights into the development of novel microbial therapy for the management of MASLD and MASH.
引用
收藏
页码:8536 / 8549
页数:14
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