Ligustrum robustum (Roxb.) blume extract modulates gut microbiota and prevents metabolic syndrome in high-fat diet-fed mice

被引:17
|
作者
Chen, Man [1 ]
Zheng, Junping [1 ]
Zou, Xiaojuan [1 ]
Ye, Cheng [4 ]
Xia, Hui [1 ]
Yang, Ming [2 ]
Gao, Qinghua [1 ]
Yang, Qingxiong [2 ]
Liu, Hongtao [1 ,3 ]
机构
[1] Hubei Univ Chinese Med, Coll Basic Med, Wuhan 430065, Hubei, Peoples R China
[2] Guizhou Normal Univ, Sch Karst Sci, State Engn Technol Inst Karst Desertificat Contro, Guiyang 550001, Peoples R China
[3] Chongqing Acad Chinese Mat Med, Nanshan Rd 34, Chongqing 400065, Peoples R China
[4] Wuhan Customs Technol Ctr, Qintai Ave 588, Wuhan 430050, Peoples R China
基金
湖北省教育厅重点项目; 中国国家自然科学基金;
关键词
Ligustrum robustum; High-fat diet; Metabolic syndrome; Glucose intolerance; Gut microbiota; TOTAL PHENYLPROPANOID GLYCOSIDES; NONALCOHOLIC STEATOHEPATITIS; OBESITY; LIVER; RESISTANCE; PROBIOTICS; HOST; TEA;
D O I
10.1016/j.jep.2020.113695
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: In Chinese folk medicine, Ligustrum robustum (Roxb.) Blume has been widely used as a healthy tea beverage for improvement in obesity and lipidemic metabolic disorders. Aim of the study: We aimed to investigate the effect of L. robustum extract (LRE) on metabolic syndrome in high fat diet (HFD)-fed mice and to explore the underlying role of gut microbiota during the treatment. Materials and methods: The ground dried leaves of L. robustum (Roxb.) Blume were extracted with ethanol and then purified by a resin column. The composition of L. robustum extract (LRE) was analyzed by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). C57BL/6 J mice fed with HFD were treated with LRE for 16 weeks. RT-qPCR and morphological staining were utilized to reveal the impact of LRE on hepatic glucolipid metabolism and gut integrity. The next-generation sequencing of 16 S rDNA was applied for analyzing the gut microbial community of fecal samples. Results: LRE, mainly composed of ligupurpuroside A and aceteoside, alleviated insulin resistance, improved hepatic metabolism, enhanced intestinal integrity, and suppressed inflammatory responses in HFD-fed mice. Moreover, LRE treatment reshaped the gut microbiota structure by increasing the levels of genera Streptococcus, Lactobacillus, and Mucispirillum and decreasing the populations of Alistipes and Lachnospiraceae NK4A136 group in HFD-fed mice. The alteration of gut microbiota was associated with several metabolic pathways of gut bacteria. Spearman's correlation analysis further confirmed the links between the changed intestinal bacteria and multiple disease indices. Conclusions: LRE prevented gut microbiota dysbiosis and metabolic disorder in HFD-fed mice, which helps to promote the application in LRE-mediated prevention from metabolic syndrome as a gut microbial regulator.
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页数:14
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