肠道菌群
失调
熊果苷
炎症
脂质代谢
代谢综合征
生物
碳水化合物代谢
代谢途径
代谢组
新陈代谢
免疫学
生物化学
内分泌学
微生物学
粪便细菌疗法
胰岛素抵抗
粪便
血脂谱
微生物代谢
内科学
化学
肥胖
作者
Cunzhen Zhao,Jiajia Li,Lituo Li,Hongxu Hou,Yuxin Zhang,Huifang Xue,Yongjie Xu
标识
DOI:10.1021/acs.jafc.5c16710
摘要
Abstract Gut microbial dysbiosis drives obesity-related metabolic disorders. This study investigated whether arbutin, a phenolic glycoside, alleviates obesity via gut microbiota modulation. In obese mice, arbutin reduced body weight, improved glucose and lipid profiles, suppressed adipogenic and inflammatory gene expression, and strengthened intestinal barrier integrity. 16S rRNA sequencing revealed elevated α-diversity and enrichment of beneficial genera including Muribaculaceae and Lactobacillus. Antibiotic depletion abolished arbutin’s antiobesity effects, whereas fecal microbiota transplantation from arbutin-treated donors recapitulated metabolic improvements and increased fecal short-chain fatty acids, including acetate, propionate, butyrate, and valerate, in a microbiota-dependent manner. Correlation analysis linked SCFA elevation to Muribaculaceae, Bacteroides, Lachnospiraceae_UCG-001, and Prevotellaceae_NK3B31_group, and KEGG enrichment implicated carbohydrate and lipid metabolism as the primary pathways affected. Collectively, these findings establish that arbutin ameliorates obesity-related inflammation and metabolic disorders via gut microbiota-derived SCFA production.
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