Sesquiterpene glycoside isolated from loquat leaf targets gut microbiota to prevent type 2 diabetes mellitus in db/db mice

被引:3
|
作者
Wu, Ruoyun [1 ]
Zhou, Lina [1 ]
Chen, Yan [1 ]
Ding, Xiaoqin [1 ]
Liu, Yan [1 ]
Tong, Bei [1 ]
Lv, Han [1 ]
Meng, Xiuhua [1 ]
Li, Jing [2 ]
Jian, Tunyu [1 ]
Chen, Jian [1 ,2 ]
机构
[1] Jiangsu Prov & Chinese Acad Sci, Inst Bot, Nanjing 210014, Peoples R China
[2] Nanjing Forestry Univ, Coll Light Ind & Food Engn, Dept Food Sci & Technol, Nanjing 210037, Peoples R China
基金
中国国家自然科学基金;
关键词
CHAIN FATTY-ACIDS; OXIDATIVE STRESS; INFLAMMATION; DIET; HYPERGLYCEMIA; METABOLISM; EXTRACT; IMPACT; RATS;
D O I
10.1039/d1fo03646g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
According to ancient records, loquat leaf has been used as both a food and medicine in China for thousands of years. Sesquiterpene glycosides from loquat leaf have achieved remarkable effects on hyperglycemia. However, their specific activities and underlying mechanisms on type 2 diabetes mellitus (T2DM) are not fully understood. In the present study, we found that SG1, a unique sesquiterpene glycoside isolated from loquat leaf, had the capability to prevent insulin resistance and inflammation. In db/db mice, SG1 administration (25 and 50 mg kg(-1) day(-1)) inhibited hyperglycemia and the release of inflammatory cytokines. To further explore the possible role of gut microbiota in SG1 for treating T2DM, we applied 16S rRNA pyrosequencing based on the V3-V4 region to analyze the fecal samples of different groups. Alpha diversity analysis showed that SG1 administration could obviously increase diversity and richness in db/db mice. At the phylum level, due to SG1 treatment, the relative abundance of Firmicutes and Actinobacteria was lowered while that of Bacteroidetes was raised. Additionally, 7 key genera in the db/db mice with SG1 supplementation were enriched: Lactobacillus, Lachnospiraceae_NK4A136_group, and Ruminococcus, Bacteroides, Prevotellaceae_UCG-001, Alistipes, and Roseburia. These findings proved that SG1 could prevent T2DM by relieving insulin resistance and inflammation and by remodeling the gut microbiota in db/db mice.
引用
收藏
页码:1519 / 1534
页数:16
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