Abstract
Chronic injury to liver triggers synthesis of extracellular matrix components resulting in progressive fibrosis and eventually cirrhosis. Transforming growth factor-β1 (TGF-β1) transduces its signal by binding to TGF-β type 1 receptor kinase or activin like kinase (ALK5) receptor and mediates hepatic fibrosis by increasing the transcription of downstream entities such as collagen via Smad2 and Smad3. The present study was carried out to investigate the mechanism by which phyllanthin, a hepatoprotective lignin isolated from the plant Phyllanthus amarus (P. amarus) exerts its anti-fibrotic effect. The inhibitory role of phyllanthin on ALK5 was first analyzed using molecular docking experiments. Phyllanthin was found to effectively bind to serine (Ser) 280 at the active site of ALK5 by forming hydrogen bonds. The in vivo protective effect of phyllanthin against carbon tetrachloride (CCl4)-induced hepatic fibrosis was established by studying the protein expressions of TGF-β1, ALK5 and Smad2 and 3 and by determining various biochemical and histopathological parameters. Phyllanthin was found to exert its anti-fibrotic effect by down-regulating TGF signaling pathway via ALK5 and Smad2 and 3 inhibition.
Acknowledgements
The authors sincerely thank Ms Aishwariya Kumaran for her valuable support in the literature collection.
Declaration of interest
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.
Funding
The fellowship assistance to Dr. Krithika Rajesh (Research Associate, File No: 45/37/BMS-TRM) from Indian Council of Medical research (ICMR), New Delhi, is acknowledged with thanks. Dr. Krithika Rajesh is also grateful to the Department of Science and Technology (DST), New Delhi, for providing financial support under Women Scientist Scheme (WOS-A): SR/WOS-A/LS-04/2013) to carry out some additional research work on the anti-fibrotic potential of phyllanthin.