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Hepatoprotective effect of bisbenzylisoquinoline alkaloid tiliamosine from Tiliacora racemosa in high-fat diet/diethylnitrosamine-induced non-alcoholic steatohepatitis
[Display omitted] •Tiliamosine, a bisbenzylisoquinoline alkaloid was isolated from Tiliacora racemose.•On HepG2 cells, tiliamosine did not exhibit any toxicity up to 100 μM.•In steatotic HepG2 cells, tiliamosine reduced lipid levels and lipotoxicity.•Treatment reduced plasma lipid and transaminase l...
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Published in: | Biomedicine & pharmacotherapy 2018-12, Vol.108, p.963-973 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Tiliamosine, a bisbenzylisoquinoline alkaloid was isolated from Tiliacora racemose.•On HepG2 cells, tiliamosine did not exhibit any toxicity up to 100 μM.•In steatotic HepG2 cells, tiliamosine reduced lipid levels and lipotoxicity.•Treatment reduced plasma lipid and transaminase levels in HFD-DEN induced animals.•Tiliamosine treated animals showed normal liver echogenicity and histology.
Non-alcoholic steatohepatitis (NASH) is one of the aggressive forms of non-alcoholic fatty liver disease (NAFLD) and is a potential risk factor of HCC. This study reports the curative effect of tiliamosine on NASH. Tiliamosine was isolated from Tiliacora racemosa Colebr. (Menispermaceae) and its structure was confirmed by studying the physical and spectroscopic data. The effects of tiliamsoine on lipid accumulation and lipotoxicity were evaluated using palmitate-oleate induced steatosis in HepG2 cells. The in vivo efficacy of tiliamosine was evaluated using HFD fed, DEN induced non-alcoholic steatohepatitis Wistar rats. In HepG2 cells, tiliamosine did not affect the cell viability up to 100 μM concentration and showed GI25 value of 264.28 μM. The treatment with tiliamsoine significantly lowered the ORO concentration by 44.17% and triglyceride accumulation by 69.32% at 50 μM concentration (P |
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ISSN: | 0753-3322 1950-6007 |
DOI: | 10.1016/j.biopha.2018.09.116 |