Alarcón B, González M E, Carrasco L
Antimicrob Agents Chemother. 1984 Nov;26(5):702-6. doi: 10.1128/AAC.26.5.702.
The antimuscarinic compound atropine shows an antiherpesvirus effect as measured by the protection of the cell monolayer and the reduction of the formation of new infectious virus. Atropine at a concentration of 200 micrograms/ml blocks the production of new infectious herpes simplex virus-type 1 virions. At that concentration, it has almost no effect on cellular or viral protein synthesis even when atropine is present from the beginning of the infection. The glycosylation of viral proteins is almost totally blocked when atropine is added. Although the viral proteins are underglycosylated, the formation of new herpes simplex virus type 1 virions takes place. The virions formed in the presence of atropine are noninfectious, and their protein composition, as assessed by labeling with [35S]methionine, is similar to that of the control, except that they are not glycosylated.
抗毒蕈碱化合物阿托品具有抗疱疹病毒的作用,这可通过保护细胞单层以及减少新的感染性病毒形成来衡量。浓度为200微克/毫升的阿托品可阻断新的感染性单纯疱疹病毒1型病毒粒子的产生。在该浓度下,即使从感染开始就存在阿托品,它对细胞或病毒蛋白合成几乎没有影响。添加阿托品时,病毒蛋白的糖基化几乎完全被阻断。尽管病毒蛋白糖基化不足,但仍会形成新的单纯疱疹病毒1型病毒粒子。在阿托品存在的情况下形成的病毒粒子没有感染性,通过用[35S]甲硫氨酸标记评估,其蛋白质组成与对照相似,只是它们没有糖基化。