Fong C K, Cohen S D, McCormick S, Hsiung G D
Antiviral Res. 1987 Jan;7(1):11-23. doi: 10.1016/0166-3542(87)90035-0.
The antiviral activity of 9-(1,3-dihydroxy-2-propoxymethyl)guanine (DHPG) against guinea pig cytomegalovirus (GPCMV) was evaluated in guinea pig cell cultures and in Hartley guinea pigs. The 50% effective dose of DHPG against GPCMV replication in cell cultures was 71 microM. Ultrastructural studies revealed that DHPG inhibited the formation of viral cores and the production of nucleocapsids, enveloped virions and dense bodies, but the drug did not prevent the formation of virus induced intranuclear tubular structures. In vivo, guinea pigs inoculated intraperitoneally with GPCMV were treated with DHPG, 25 mg/kg subcutaneously, twice daily. Treatment was initiated 24 h after infection and continued for 7 days. During the acute infection, the average body weights of DHPG-treated, virus infected guinea pigs were approximately 14% lower than the sham-treated counterparts on day 10, 11 and 13 post-virus inoculation. Virus infectivity titers were higher in the lungs of DHPG-treated guinea pigs on day 10 than the sham-treated ones. Although there was no significant difference on histopathologic lesions in the spleen, liver and lungs of the drug-treated and the sham-treated guinea pigs, DHPG treated animals appeared to have fewer virus-induced lesions or inclusions in the kidneys and salivary glands than the sham-treated ones. In addition, virus infectivity titers in the salivary gland of DHPG treated guinea pigs were consistently lower than the sham-treated animals.
在豚鼠细胞培养物和Hartley豚鼠中评估了9-(1,3-二羟基-2-丙氧基甲基)鸟嘌呤(DHPG)对豚鼠巨细胞病毒(GPCMV)的抗病毒活性。DHPG在细胞培养物中对GPCMV复制的50%有效剂量为71微摩尔。超微结构研究表明,DHPG抑制病毒核心的形成以及核衣壳、包膜病毒粒子和致密体的产生,但该药物并未阻止病毒诱导的核内管状结构的形成。在体内,腹腔接种GPCMV的豚鼠皮下注射DHPG,剂量为25毫克/千克,每日两次。在感染后24小时开始治疗,并持续7天。在急性感染期间,在病毒接种后第10、11和13天,接受DHPG治疗的病毒感染豚鼠的平均体重比假治疗组低约14%。在第10天,接受DHPG治疗的豚鼠肺部的病毒感染滴度高于假治疗组。虽然在药物治疗组和假治疗组豚鼠的脾脏、肝脏和肺部的组织病理学病变上没有显著差异,但与假治疗组相比,接受DHPG治疗的动物在肾脏和唾液腺中似乎有较少的病毒诱导病变或包涵体。此外,接受DHPG治疗的豚鼠唾液腺中的病毒感染滴度始终低于假治疗组动物。