Tang Mi, Li Xianping, Ren Jiahui, Yao Chunyu, Liu Lu, Li Xiaojing, Yuan Xueping, Zhao Junying, Liu Bin, Qiao Weicang, Chen Lijun
Key Laboratory of Dairy Science, Ministry of Education, Food Science College, Northeast Agricultural University, Harbin, China.
National Engineering Research Center of Dairy Health for Maternal and Child, Beijing Sanyuan Foods Co., Ltd., Beijing, China.
Front Nutr. 2025 Jun 25;12:1597334. doi: 10.3389/fnut.2025.1597334. eCollection 2025.
Obesity is a globally prevalent metabolic disease, and high-calorie diets are major contributors to its development. Probiotic interventions can modulate the gut flora and alleviate systemic and low-grade inflammation, making them potential in-terventions for alleviating metabolic syndrome.
This study explored the beneficial effects of the HM108 strain derived from breast milk on obesity in high-fat diet-induced rats using a multi-gradient concentration in-tervention. Serum biochemical markers and inflammatory mediators were determined using enzyme-linked immunosorbent assay after 6-week intervention. Gut microbiota was assessed using 16S rRNA sequencing. The levels of short-chain fatty acid were detected using gas chromatography-mass spectrometry, fecal metabolites were ana-lysed using untargeted metabolomics, and the liver tissue was subjected to tran-scriptomics analysis.
The findings indicated that HM108 mitigated obesity, reduced blood lipids levels and immune factors, as well as altered the gut mi-crobiota composition, including reducing the Firmicutes/Bacteroidetes ratio. HM108 also inhibited the JAK-STAT signalling pathway. HM108 alleviates obesity caused by a high-fat diet in rats, offering a theoretical foun-dation and practical insights for utilizing this strain in obesity management.
肥胖是一种全球流行的代谢性疾病,高热量饮食是其发展的主要促成因素。益生菌干预可调节肠道菌群,减轻全身和低度炎症,使其成为缓解代谢综合征的潜在干预措施。
本研究采用多梯度浓度干预,探讨源自母乳的HM108菌株对高脂饮食诱导的大鼠肥胖的有益作用。干预6周后,采用酶联免疫吸附测定法测定血清生化标志物和炎症介质。使用16S rRNA测序评估肠道微生物群。采用气相色谱-质谱联用仪检测短链脂肪酸水平,采用非靶向代谢组学分析粪便代谢物,并对肝脏组织进行转录组学分析。
研究结果表明,HM108减轻了肥胖,降低了血脂水平和免疫因子,还改变了肠道微生物群组成,包括降低厚壁菌门与拟杆菌门的比例。HM108还抑制了JAK-STAT信号通路。HM108减轻了大鼠高脂饮食引起的肥胖,为在肥胖管理中利用该菌株提供了理论基础和实践见解。