Probiotic Mixture Ameliorates a Diet-Induced MASLD/MASH Murine Model through the Regulation of Hepatic Lipid Metabolism and the Gut Microbiome.
Fangfei ZhangEmily Kwun Kwan LoJiarui ChenKe Wang FeliciannaMarsena Jasiel IsmaiahHoi Kit Matthew LeungDanyue ZhaoJetty Chung-Yung LeeHani El-NezamiPublished in: Journal of agricultural and food chemistry (2024)
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.
Keyphrases
- high fat diet
- insulin resistance
- adipose tissue
- high fat diet induced
- oxidative stress
- diabetic rats
- high glucose
- risk factors
- fatty acid
- randomized controlled trial
- signaling pathway
- drug induced
- systematic review
- metabolic syndrome
- type diabetes
- mouse model
- skeletal muscle
- combination therapy
- climate change
- lactic acid
- liver fibrosis
- wild type
- human health