Celastrus orbiculatus Thunb. extracts and celastrol alleviate NAFLD by preserving mitochondrial function through activating the FGF21/AMPK/PGC-1α pathway

被引:2
作者
Xue, Junli [1 ]
Liu, Yunchao [2 ]
Liu, Boyan [1 ]
Jia, Xiubin [2 ]
Fang, Xinsheng [3 ]
Qin, Shucun [1 ]
Zhang, Ying [2 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Affiliated Hosp 2, Taishan Inst Hydrogen Biomed, Tai An, Shandong, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Sch Pharmaceut Sci, Jinan, Shandong, Peoples R China
[3] Shandong Agr Univ, Coll Agron, Tai An, Shandong, Peoples R China
关键词
Celastrus orbiculatus Thunb; celastrol; NAFLD; mitochondrial function; FGF21/AMPK/PGC-1; alpha; HIGH-FAT DIET; HEPATIC STEATOSIS; OXIDATIVE STRESS; LIPID-ACCUMULATION; AMPK; DYSFUNCTION; OBESITY; MICE; SIRT3; PATHOGENESIS;
D O I
10.3389/fphar.2024.1444117
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Non-alcoholic fatty liver disease (NAFLD) is a prevalent chronic liver disease globally, characterized by the accumulation of lipids, oxidative stress, and mitochondrial dysfunction in the liver. Celastrus orbiculatus Thunb. (COT) and its active compound celastrol (CEL) have demonstrated antioxidant and anti-inflammatory properties. Our prior research has shown the beneficial effects of COT in mitigating NAFLD induced by a high-fat diet (HFD) in guinea pigs by reducing hepatic lipid levels and inhibiting oxidative stress. This study further assessed the effects of COT on NAFLD and explored its underlying mitochondria-related mechanisms. Methods: COT extract or CEL was administered as an intervention in C57BL/6J mice fed a HFD or in HepG2 cells treated with sodium oleate. Oral glucose tolerance test, biochemical parameters including liver enzymes, blood lipid, and pro-inflammatory factors, and steatosis were evaluated. Meanwhile, mitochondrial ultrastructure and indicators related to oxidative stress were tested. Furthermore, regulators of mitochondrial function were measured using RT-qPCR and Western blot. Results: The findings demonstrated significant reductions in hepatic steatosis, oxidative stress, and inflammation associated with NAFLD in both experimental models following treatment with COT extract or CEL. Additionally, improvements were observed in mitochondrial structure, ATP content, and ATPase activity. This improvement can be attributed to the significant upregulation of mRNA and protein expression levels of key regulators including FGF21, AMPK, PGC-1 alpha, PPAR gamma, and SIRT3. Conclusion: These findings suggest that COT may enhance mitochondrial function by activating the FGF21/AMPK/PGC-1 alpha signaling pathway to mitigate NAFLD, which indicated that COT has the potential to target mitochondria and serve as a novel therapeutic option for NAFLD.
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页数:16
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