Heijtink R A, De Wilde G A, Kruining J, Berk L, Balzarini J, De Clercq E, Holy A, Schalm S W
Department of Virology, Erasmus University Rotterdam, The Netherlands.
Antiviral Res. 1993 Jun;21(2):141-53. doi: 10.1016/0166-3542(93)90050-s.
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) was evaluated for its inhibitory effect on hepadnavirus replication in three different cell systems, i.e., human hepatoma cell lines HepG2 2.2.15 and HB611 (transfected with human hepatitis B virus (HBV)) and primary cultures of duck hepatocytes infected with duck hepatitis B virus (DHBV). PMEA inhibited HBV release from HepG2 2.2.15 cells and HB611 cells at a 50% inhibitory concentration (IC50) of 0.7 and 1.2 microM, respectively. Intracellular viral DNA synthesis was inhibited at concentrations equivalent to those required to inhibit virus release from the cells. DHBV secretion from duck hepatocytes was inhibited by PMEA at an IC50 of 0.2 microM. HBsAg secretion was inhibited by PMEA in a concentration-dependent manner in HB611 cells and DHBV-infected duck hepatocytes but not HepG2 2.2.15 cells. The 50% cytotoxic concentration, as measured by inhibition of [3H-methyl]deoxythymidine incorporation was 150 microM for the two human hepatoma cell lines and 40 microM for the duck hepatocyte cultures. In a pilot experiment PMEA was found to reduce the amounts of DHBV DNA in the serum of Pekin ducks.
对9-(2-膦酰甲氧基乙基)腺嘌呤(PMEA)在三种不同细胞系统中对嗜肝DNA病毒复制的抑制作用进行了评估,这三种细胞系统分别是人肝癌细胞系HepG2 2.2.15和HB611(转染了人乙型肝炎病毒(HBV))以及感染鸭乙型肝炎病毒(DHBV)的鸭肝细胞原代培养物。PMEA抑制HepG2 2.2.15细胞和HB611细胞释放HBV,其50%抑制浓度(IC50)分别为0.7和1.2微摩尔。在与抑制病毒从细胞中释放所需浓度相当的浓度下,细胞内病毒DNA合成受到抑制。PMEA以0.2微摩尔的IC50抑制鸭肝细胞分泌DHBV。在HB611细胞和感染DHBV的鸭肝细胞中,PMEA以浓度依赖的方式抑制HBsAg分泌,但在HepG2 2.2.15细胞中则不然。通过抑制[3H-甲基]脱氧胸苷掺入来测量,两种人肝癌细胞系的50%细胞毒性浓度为150微摩尔;鸭肝细胞培养物的50%细胞毒性浓度为40微摩尔。在一项初步实验中,发现PMEA可减少北京鸭血清中DHBV DNA的量。