Nikolaeva I S, Fomina A N
Antibiot Khimioter. 1988 Jun;33(6):455-9.
It was shown for the first time that the antiviral drug bonafton administered orally to nonlinear albino mice in single doses of 5, 12.5 and 25 mg/kg induced production of interferon in the animal blood serum. The maximum interferon titer of 160-320 IU/ml was observed 18 hours after the drug administration in a dose of 12.5 mg/kg. In low doses of 5 to 12.5 mg/kg bonafton increased the nonspecific resistance of the mice to experimental viral infections when administered orally in single doses not earlier than 2 weeks prior to the contamination. The ability of the drug to stimulate the host protective forces probably plays a certain role in the mechanism of its therapeutic action in severe viral infections of man such as severe recurring ophthalmic herpes, genital herpes, Behçet's disease, Melkersson-Rosenthal syndrome and others.
首次表明,以5、12.5和25毫克/千克的单剂量口服给予非线性白化小鼠抗病毒药物博纳夫通,可诱导动物血清中产生干扰素。在以12.5毫克/千克的剂量给药后18小时,观察到最大干扰素滴度为160 - 320国际单位/毫升。当在感染前不早于2周以单剂量口服给药时,低剂量(5至12.5毫克/千克)的博纳夫通可增强小鼠对实验性病毒感染的非特异性抵抗力。该药物刺激宿主保护力的能力可能在其对人类严重病毒感染(如严重复发性眼部疱疹、生殖器疱疹、白塞病、梅尔克森 - 罗森塔尔综合征等)的治疗作用机制中发挥一定作用。