Xing Lu, Zeng Rui, Huang Kai, Xue Jingbo, Liu Hongliang, Zhao Zhimin, Peng Yuan, Hu Xudong, Liu Chenghai
Institute of Liver diseases, Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of Biology, School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2022 Sep 26;13:907921. doi: 10.3389/fphar.2022.907921. eCollection 2022.
Fuzheng Huayu Recipe (FZHY) is a Chinese patent medicine (approval No. Z20020074) included in the national medical insurance catalogue, which is mainly used for anti-hepatic fibrosis treatment of hepatitis B virus (HBV) induced liver fibrosis and liver cirrhosis. In clinical practice, we discovered that FZHY might also have a direct anti-HBV effect on inhibiting HBeAg production, but the mechanism underlying was unclear. This study aimed to clarify the molecular mechanism of the inhibition effect of FZHY on HBeAg production. The decrease degree of serum HBeAg titer in FZHY + entecavir (ETV) group patients were analyzed through clinical data. C57BL/6N-Tg (1.28HBV)/Vst HBV transgenic mice were used for experiments. HepG2. 2.15 cells (wild-type HBV replication cells) were used for experiments. The clinical study results showed that the decrease degree of serum HBeAg titer in FZHY+ETV group was significantly higher than that in ETV group after 48 weeks treatment. experiments results showed that FZHY could significantly reduce the serum HBeAg titer in HBV transgenic mice, and promote HBeAg seroconversion. experiments results showed that FZHY could reduce HBeAg titer dependently, but it did not significantly inhibit the expression of HBsAg and HBV-DNA. Further cell experiments discovered that TOMM34 might be the key target for FZHY to inhibit HBeAg production. The subsequent pharmacological screening experiment of 20 active compounds in FZHY showed that quercetin, baicalin and cordycepin could promote the expression of TOMM34 gene and reduce the production of HBeAg. In conclusion, FZHY and its active compounds quercetin, baicalin and cordycepin could inhibit HBeAg production by promoting the expression of TOMM34 gene in HBV-infected hepatocytes.
扶正化瘀方(FZHY)是一种被纳入国家医保目录的中成药(批准文号:Z20020074),主要用于乙肝病毒(HBV)所致肝纤维化和肝硬化的抗肝纤维化治疗。在临床实践中,我们发现扶正化瘀方可能对抑制HBeAg产生也有直接抗HBV作用,但其潜在机制尚不清楚。本研究旨在阐明扶正化瘀方抑制HBeAg产生的分子机制。通过临床数据分析扶正化瘀方联合恩替卡韦(ETV)组患者血清HBeAg滴度的下降程度。使用C57BL/6N-Tg(1.28HBV)/Vst HBV转基因小鼠进行实验。使用HepG2.2.15细胞(野生型HBV复制细胞)进行实验。临床研究结果显示,治疗48周后,扶正化瘀方联合恩替卡韦组血清HBeAg滴度的下降程度显著高于恩替卡韦组。实验结果显示,扶正化瘀方可显著降低HBV转基因小鼠血清HBeAg滴度,并促进HBeAg血清学转换。实验结果显示,扶正化瘀方可依赖性降低HBeAg滴度,但对HBsAg和HBV-DNA的表达无显著抑制作用。进一步的细胞实验发现,TOMM34可能是扶正化瘀方抑制HBeAg产生的关键靶点。随后对扶正化瘀方中20种活性成分进行的药理筛选实验表明,槲皮素、黄芩苷和虫草素可促进TOMM34基因表达并降低HBeAg产生。综上所述,扶正化瘀方及其活性成分槲皮素、黄芩苷和虫草素可通过促进HBV感染肝细胞中TOMM34基因的表达来抑制HBeAg产生。