Zhang Hongfa, Xu Yu, Li Mingjie, Chen Zhaowei, Wang Yuezhu, Yang Rongfu, Li Sheng, Ma Shiyu, You Chunping, Zheng Huajun
State Key Laboratory of Dairy Biotechnology, Shanghai Engineering Research Center of Dairy Biotechnology Dairy Research Institute, Bright Dairy & Food Co., Ltd., Synergetic Innovation Center of Food Safety and Nutrition Shanghai China.
Shanghai-MOST Key Laboratory of Health and Disease Genomics, NHC Key Lab of Reproduction Regulation Shanghai Institute for Biomedical and Pharmaceutical Technologies Shanghai China.
Food Sci Nutr. 2025 Aug 6;13(8):e70728. doi: 10.1002/fsn3.70728. eCollection 2025 Aug.
This study aimed to investigate the effects of () ST-Ⅲ and oats supplementation on high-fat diet (HFD)-induced obesity in rats, focusing on changes in body weight, organ/fat tissue weights, inflammatory markers, serum parameters, and gut microbiota composition. Male Sprague-Dawley rats ( ≥ 6/group) were fed a normal diet (ND) or HFD for 9 weeks to establish obesity. Then, HFD-fed rats were divided into four groups: HFD + ST-Ⅲ, ND + ST-Ⅲ, HFD + Oats, and ND + Oats, receiving daily oral gavage of ST-III (1.5 × 10 CFU/rat) or oats for another 9 weeks. Body weight, serum lipids, cytokines (e.g., IL-6, PYY, and MCP-1), liver histopathology, and gut microbiota were analyzed. Notably, weight loss is primarily influenced by diet, and better results can be achieved by controlling diet in combination with new edible ST-Ⅲ in promoting weight loss. ST-Ⅲ reduced the levels of the factors CORT and MCP-1, thereby potentially promoting weight loss. The ST-Ⅲ group showed earlier weight reduction (significant at Week 2) than the oats group (at Week 6). Gut microbiota analysis revealed differential abundances of , , and between intervention groups. No significant differences in liver or organ weights were observed. ST-Ⅲ and oats attenuated HFD-induced obesity by modulating metabolic parameters, inflammation, and gut microbiota. ST-Ⅲ exhibited quicker anti-obesity effects, while oats enhanced probiotic growth. Dietary structure improvement remains critical for weight management. Further studies should address stress-related experimental limitations and explore clinical applications.
本研究旨在探讨补充()ST-Ⅲ和燕麦对高脂饮食(HFD)诱导的大鼠肥胖的影响,重点关注体重、器官/脂肪组织重量、炎症标志物、血清参数和肠道微生物群组成的变化。将雄性斯普拉格-道利大鼠(每组≥6只)喂食正常饮食(ND)或HFD 9周以建立肥胖模型。然后,将喂食HFD的大鼠分为四组:HFD + ST-Ⅲ、ND + ST-Ⅲ、HFD + 燕麦和ND + 燕麦,连续9周每天口服灌胃ST-III(1.5×10 CFU/只大鼠)或燕麦。分析了体重、血脂、细胞因子(如IL-6、PYY和MCP-1)、肝脏组织病理学和肠道微生物群。值得注意的是,体重减轻主要受饮食影响,在促进体重减轻方面,通过控制饮食结合新的可食用ST-Ⅲ可取得更好的效果。ST-Ⅲ降低了CORT和MCP-1因子的水平,从而可能促进体重减轻。ST-Ⅲ组比燕麦组(第6周)更早出现体重减轻(第2周显著)。肠道微生物群分析显示干预组之间、和的丰度存在差异。未观察到肝脏或器官重量有显著差异。ST-Ⅲ和燕麦通过调节代谢参数、炎症和肠道微生物群减轻了HFD诱导的肥胖。ST-Ⅲ表现出更快的抗肥胖作用,而燕麦促进了益生菌的生长。改善饮食结构对体重管理仍然至关重要。进一步的研究应解决与应激相关的实验局限性并探索临床应用。