Zhao Tong-Shi-Yao, Li Kang-Zhi, Su He-Ling, Liang Bin, Liang Cheng-Qin, Gao Jin-Tao, Zhou Xian-Li
Key Laboratory of Molecular Medical Engineering, Education Department of Guangxi Zhuang Autonomous Region, Guilin Medical University, Guilin 541100, China.
College of Pharmacy, Guilin Medical University, Guilin 541100, China.
Molecules. 2025 May 6;30(9):2063. doi: 10.3390/molecules30092063.
Hepatitis B is a serious infectious disease that threatens the health of all mankind. In this study, we isolated and extracted hydroxytyrosol from with anti-hepatitis B virus (HBV) activity. The structure of hydroxytyrosol was identified by the nuclear magnetic resonance technique. HepG2.2.15 cell models were used to detect the anti-HBV activity and liver protection of hydroxytyrosol in vitro. Hydroxytyrosol can inhibit hepatitis B surface antigen (HBsAg) and hepatitis B e-antigen (HBeAg). The IC values of HBsAg and HBeAg were 4.02 mg/L and 5.19 mg/L, respectively. At the highest concentration of hydroxytyrosol, the inhibition rates of supernatant and intracellular HBV DNA were 75.99% and 66.33%, respectively. Hydroxytyrosol was less toxic to normal human hepatocytes. Molecular docking showed that hydroxytyrosol was bound to three amino acid residues of HBV polymerase with a binding energy of -7.0 kcal/mol. This study provided data for the development and utilization of and the research and development of anti-hepatitis B virus drugs.
乙型肝炎是一种严重威胁全人类健康的传染病。在本研究中,我们从[未提及的来源]中分离提取了具有抗乙型肝炎病毒(HBV)活性的羟基酪醇。通过核磁共振技术鉴定了羟基酪醇的结构。采用HepG2.2.15细胞模型体外检测羟基酪醇的抗HBV活性和肝脏保护作用。羟基酪醇可抑制乙型肝炎表面抗原(HBsAg)和乙型肝炎e抗原(HBeAg)。HBsAg和HBeAg的半数抑制浓度(IC)值分别为4.02mg/L和5.19mg/L。在羟基酪醇的最高浓度下,上清液和细胞内HBV DNA的抑制率分别为75.99%和66.33%。羟基酪醇对正常人肝细胞的毒性较小。分子对接显示,羟基酪醇与HBV聚合酶的三个氨基酸残基结合,结合能为-7.0千卡/摩尔。本研究为[未提及的来源]的开发利用及抗乙型肝炎病毒药物的研发提供了数据。