Extract ofSchisandra chinensisfruit protects against metabolic dysfunction in high-fat diet induced obese mice viaFXRactivation

被引:10
|
作者
Gu, Ming [1 ,2 ]
Song, Haiyan [1 ]
Li, Yiping [1 ]
Jiang, Yuwei [1 ]
Zhang, Yali [1 ]
Tang, Zhipeng [1 ]
Ji, Guang [1 ]
Huang, Cheng [2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Digest Dis, Longhua Hosp, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Sch Pharm, Shanghai 201203, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
farnesoid X receptor; metabolic syndrome; non-alcoholic fatty liver disease; obesity; Schisandra chinensisfruit; X-RECEPTOR AGONIST; NUCLEAR RECEPTOR; ADIPOKINES; DISEASE; LIGNANS; GW4064; MODELS; FRUIT; ACID;
D O I
10.1002/ptr.6743
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Schisandra chinensisfruit has been shown to restore carbohydrate- and lipid-metabolic disorders and has anti-hepatotoxicity and anti-hepatitis activities. However, the molecular targets mediating the pharmacological properties ofS.chinensisfruit have not been clarified. Here, we assayed the effects ofS.chinensisfruit ethanol extract (SCE) on farnesoid X receptor (FXR) transactivity. The pharmacological effects of SCE (1 g/100 g diet) were assessed in high-fat diet (HFD)-fed C57BL/6 mice and ob/ob mice. The FXR and Fgf15 signalling pathways were evaluated by FXR silencing, ELISA, Western blot and RT-PCR analyses. The results showed that SCE treatment increased FXR transcription activity and improved obesity, hypercholesteremia and fatty liver in HFD-fed mice, while it had limited effects on ob/ob mice. Our study suggests that SCE treatment may improve HFD-induced metabolic disorders through pharmacological activation of FXR/Fgf15 signalling, and such beneficial effects of SCE may require leptin participation.
引用
收藏
页码:3063 / 3077
页数:15
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