Stenberg K, Larsson A
Antimicrob Agents Chemother. 1978 Nov;14(5):727-30. doi: 10.1128/AAC.14.5.727.
The antiviral compound trisodium phosphonoformate (PFA), which inhibits herpesvirus multiplication by 50% at a concentration of 10 muM, did not show any effects on macromolecular synthesis and cell proliferation in HeLa and human lung cells at this concentration. At the high concentration of 2 mM, PFA reduced DNA synthesis to 50% after 1 h of treatment, whereas no effects could be seen on RNA and protein synthesis. Treatment for 24 h with 1 mM PFA inhibited both DNA synthesis and cell proliferation to 50%. The inhibition of DNA synthesis and cell proliferation at 10 mM PFA was rapidly reversed by removing the drug from the cells.
抗病毒化合物膦甲酸钠三钠(PFA)在浓度为10 μM时可使疱疹病毒增殖抑制50%,但在此浓度下对HeLa细胞和人肺细胞中的大分子合成及细胞增殖无任何影响。在2 mM的高浓度下,处理1小时后PFA可使DNA合成降至50%,而对RNA和蛋白质合成无影响。用1 mM PFA处理24小时可使DNA合成和细胞增殖均抑制50%。通过从细胞中去除药物,10 mM PFA对DNA合成和细胞增殖的抑制作用可迅速逆转。