Inonotus obliquus and its bioactive compounds alleviate non-alcoholic fatty liver disease via regulating FXR/SHP/SREBP-1c axis

被引:13
|
作者
Peng, Ankang [1 ,2 ,3 ]
Liu, Shunzhi [5 ]
Fang, Lu [1 ,2 ,3 ]
Zhu, Zixing [1 ,2 ,3 ]
Zhou, Yuan [4 ]
Yue, Shanshan [1 ,2 ,3 ]
Ma, Zejiang [1 ,2 ,3 ]
Liu, Xiaoang [1 ,2 ,3 ]
Xue, Shilin [1 ,2 ,3 ]
Qiu, Yingkun [5 ]
Qi, Rong [1 ,2 ,3 ,6 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Pharmacol, Hlth Sci Ctr, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[2] Peking Univ, Key Lab Mol Cardiovasc Sci, Minist Educ, Beijing, Peoples R China
[3] Peking Univ, Beijing Key Lab Mol Pharmaceut & New Drug Deliver, Beijing, Peoples R China
[4] Peking Univ, Sch Basic Med Sci, Dept Biomed Informat, MOE Key Lab Cardiovasc Sci, Beijing, Peoples R China
[5] Xiamen Univ, Sch Pharmaceut Sci, State Key Lab Cellular Stress Biol, South Xiang An Rd, Xiamen 361102, Peoples R China
[6] Fujian Prov Key Lab Hepat Drug Res, Fuzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Inonotus obliquus; NAFLD; Inotodiol; FXR; Lipogenesis; PATHOGENESIS; POLYSACCHARIDE; METABOLISM; NAFLD; ANTIOXIDANT; STEATOSIS; ACIDS; MICE;
D O I
10.1016/j.ejphar.2022.174841
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) is currently the most common chronic liver disease worldwide. However, there is still lack of specific drugs for treating NAFLD in clinic. Inonotus obliquus (IO), a folk medicinal fungus, has long been used to prevent against metabolic syndrome related diseases, such as hypertension and diabetes, etc. However, the study of IO anti-NAFLD effect has been reported rarely. This study aimed to investigate whether IO has an inhibitory effect on NAFLD, identify the active compounds in IO and clarify the underlying mechanisms of its anti-NAFLD effects. The results of Oil Red O(ORO) and Hematoxylin-Eosin (HE) staining, lipid extraction and determination showed that IO and its extracts, including inotodiol (Ino), lanosterol (Lan) and trametenolic acid (TA), could remarkably ameliorate lipid accumulation in MCD diet-induced mouse livers or OA-induced LO2 hepatocytes. Moreover, qPCR analysis revealed that IO and its compounds significantly downregulated the mRNA levels of lipogenic genes, such as SREBP-1c, ACC1 and FASN, and upregulated the mRNA levels of FXR and SHP. We found that the administration of guggulsterone (GS), a FXR inhibitor, abolished the inhibitory effect of Ino on lipid deposition in OA-induced LO2 cells. In conclusion, IO and its compounds attenuate hepatic lipid accumulation in NAFLD by inhibiting liver lipogenesis. The anti-NAFLD effects of Ino, a bioactive compound in IO, are through regulating FXR/SHP/SREBP-1c pathway. Our results suggested that IO and its bioactive compound Ino may become promising drugs to treat NAFLD.
引用
收藏
页数:11
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