Aucubin and its hydrolytic derivative attenuate activation of hepatic stellate cells via modulation of TGF-beta stimulation

作者:Lv, Pei-Yu; Feng, Han; Huang, Wei-Hua; Tian, Ying-Ying; Wang, Ya-Qin; Qin, Yu-hua; Li, Xiao-Hui; Hu, Kai; Zhou, Hong-Hao; Ouyang, Dong-Sheng*
来源:Environmental Toxicology and Pharmacology, 2017, 50: 234-239.
DOI:10.1016/j.etap.2017.02.012

摘要

Eucommia ulmoides is an important traditional Chinese medicine and has been used as a tonic with a long history. Aucubin is an active component extracted from Eucommia ulmoides, which has liver protection effects. However the mechanisms are still unclear. To investigate the inhibitory effects and the underlying mechanisms of aucubin on TGF-beta 1-induced activation of hepatic stellate cells and ECM deposition, Human hepatic stellate cells (LX-2 cells) were incubated with TGF-I31 to evaluate the anti fibrotic effect of aucubin. Western blot was used to investigate the expression of a-SMA, Col I, Col III, MMP2 and TIMP-1. ROS production was monitored using DCFH-DA probe, and NOX4 expression was detected by Real-time PCR. Results indicated that TGF-p1 stimulated the activation and ECM deposition of LX-2 cells. Compared with the control group, aucubin and aucubigenin both reduced the protein expression of alpha-SMA, Col I, Col III and MMP-2 in LX-2 cells. Aucubin and aucubigenin also suppressed the generation of ROS and down-regulated the NOX4 mRNA expression. Taken together, aucubin and aucubigenin both inhibit the activation and ECM deposition of LX-2 cells activated by TGF-beta 1. Aucubin and aucubigenin are potential therapeutic candidate drugs for liver fibrosis.