Oroxylin A inhibits ethanol‐induced hepatocyte senescence via YAP pathway. (10th January 2018)

• Record Type: Journal Article
• Authors: Jin, Huanhuan; Lian, Naqi; Bian, Mianli; Zhang, Chenxi; Chen, Xingran; Shao, Jiangjuan; Wu, Li; Chen, Anping; Guo, Qinglong; Zhang, Feng; Zheng, Shizhong
• Is Part Of: Cell proliferation. Volume 51:Number 3(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-01-10
• Subjects: Cell proliferation -- Periodicals; 571.84
• DOI: 10.1111/cpr.12431
• Languages: English
• ISSNs: 0960-7722

Abstract

Abstract: Objectives: Oroxylin A, a natural flavonoid isolated from Scutellaria baicalensis, has been reported to have anti‐hepatic injury effects. However, the effects of oroxylin A on alcoholic liver disease (ALD) remains unclear. The aim of this study was to elucidate the effects of oroxylin A on ALD and the potential mechanisms. Materials and methods: Male ICR mice and human hepatocyte cell line LO2 were used. Yes‐associated protein (YAP) overexpression and knockdown were achieved using plasmid and siRNA technique. Cellular senescence was assessed by analyses of the senescence‐associated β‐galactosidase (SA‐β‐gal), senescence marker p16, p21, Hmga1, cell cycle and telomerase activity. Results: Oroxylin A alleviated ethanol‐induced hepatocyte damage by suppressing activities of supernatant marker enzymes. We found that oroxylin A inhibited ethanol‐induced hepatocyte senescence by decreasing the number of SA‐β‐gal‐positive LO2 cells and reducing the expression of senescence markers p16, p21 and Hmga1 in vitro. Moreover, oroxylin A affected the cell cycle and telomerase activity. Of importance, we revealed that YAP pharmacological inhibitor verteporfin or YAP siRNA eliminated the effect of oroxylin A on ethanol‐induced hepatocyte senescence in vitro, and this was further supported by the evidence in vivo experiments. Conclusion: Therefore, these aggregated data suggested that oroxylin A relieved alcoholic liver injury possibly by inhibiting the senescence of hepatocyte, which was dependent on its activation of YAP in hepatocytes.