Exploring Anti-Nonalcoholic Fatty Liver Disease Mechanism of Gardeniae Fructus by Network Pharmacology, Molecular Docking, and Experiment Validation

被引:12
|
作者
Tang, Zhongyan [1 ]
Li, Lin [2 ]
Xia, Zhengxiang [3 ]
机构
[1] Fudan Univ, Jin Shan Hosp, Dept Emergency & Crit Care Med, Shanghai 201508, Peoples R China
[2] Tongji Univ, Shanghai Engn Res Ctr Tooth Restorat & Regenerat, Sch & Hosp Stomatol, Dept Operat Dent & Endodont, Shanghai 200072, Peoples R China
[3] Tongji Univ, Shanghai Engn Res Ctr Tooth Restorat & Regenerat, Sch & Hosp Stomatol, Dept Pharm, Shanghai 200072, Peoples R China
来源
ACS OMEGA | 2022年 / 7卷 / 29期
关键词
GAMMA; RATS;
D O I
10.1021/acsomega.2c02629
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gardeniae fructus (GF), the fruit from Gardenia jasminoides Ellis, is a traditional Chinese medicine used for the treatment of nonalcoholic fatty liver disease (NAFLD) in the clinic. To explore the hepatoprotective mechanism of GF for the treatment of NAFLD, we proposed a novel strategy that integrated in vivo efficacy evaluation, network pharmacology analysis, molecular docking, and experimental validation. A NAFLD animal model induced by high fat diet (HFD) feed was established, then orally administrated with or without GF. The results showed that GF significantly decreased the levels of serum total cholesterol (TC), lipoprotein cholesterol, triglyceride (TG), alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase, free fatty acids, glucose, and insulin and the levels of liver TG, TC, and malondialdehyde compared with the nontreated HFD group. Network pharmacology studies showed that quercetin, oleanolic acid, kaempferol, and geniposide were the main biocompounds in GF that targeted the PPAR alpha and PPAR gamma genes through regulating the PPAR and AMPK signal pathways to protect against NAFLD. The interactions between bioactive compounds and their corresponding target proteins were analyzed by molecular docking and subsequently confirmed using the qRT-PCR assay. Collectively, GF was a therapeutic drug for the treatment of NAFLD.
引用
收藏
页码:25521 / 25531
页数:11
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