多糖和/或复合多糖的饮食干预重塑高脂饮食诱导肥胖小鼠的肝脏脂质谱并改善肠道代谢紊乱
Dietary Interventions with Polysaccharides and/or Composite Polysaccharides Remodel Liver Lipid Profiles and Ameliorate Gut Metabolic Disturbances in High-Fat Diet-Induced Obese Mice.
作者信息
Zhang Peiting, Dong Jinjin, Lu Jiamin, Cai Zijian, Zhou Bingde, Zhang Qian, Zhu Chenglin, Laghi Luca
机构信息
College of Pharmacy and Food, Southwest Minzu University, Chengdu 610041, China.
Department of Agricultural and Food Sciences, University of Bologna, 47521 Cesena, Italy.
出版信息
Foods. 2025 Jul 29;14(15):2653. doi: 10.3390/foods14152653.
The global obesity epidemic and associated metabolic disorders present urgent public health challenges. This study employed a multi-omics approach (lipidomics, metabolomics, and gut microbiome analysis) to investigate how polysaccharides (BSPs) and composite polysaccharides modulate liver lipid metabolism and gut microbiota in high-fat diet (HFD)-induced obese mice. HFD elevated hepatic phosphatidylcholines, cholesteryl esters (CEs), and acylcarnitines (CARs), alongside increased cecal choline and trimethylamine. BSP interventions reduced hepatic CEs, free fatty acids (FAs), CARs, and cecal sarcosine while restoring gut microbial diversity. Notably, BSP enriched beneficial genera, including and , and the network analysis revealed negative correlations between these genera and hepatic triglycerides (TGs), implicating the gut-liver axis in lipid metabolism regulation. These findings elucidate the anti-obesity mechanisms of polysaccharides through gut microbiota remodeling and cross-tissue metabolic interactions, providing a foundation for leveraging plant polysaccharides in developing safer, effective obesity therapies.
全球肥胖流行及相关代谢紊乱带来了紧迫的公共卫生挑战。本研究采用多组学方法(脂质组学、代谢组学和肠道微生物组分析)来探究多糖(BSPs)和复合多糖如何调节高脂饮食(HFD)诱导的肥胖小鼠的肝脏脂质代谢和肠道微生物群。HFD使肝脏磷脂酰胆碱、胆固醇酯(CEs)和酰基肉碱(CARs)升高,同时盲肠胆碱和三甲胺增加。BSP干预降低了肝脏CEs、游离脂肪酸(FAs)、CARs和盲肠肌氨酸,同时恢复了肠道微生物多样性。值得注意的是,BSP富集了有益菌属,包括和,网络分析显示这些菌属与肝脏甘油三酯(TGs)之间呈负相关,提示肠道-肝脏轴参与脂质代谢调节。这些发现阐明了多糖通过重塑肠道微生物群和跨组织代谢相互作用的抗肥胖机制,为利用植物多糖开发更安全、有效的肥胖治疗方法奠定了基础。