[病毒唑对poly(G) X poly(C)等多核苷酸干扰素抗病毒活性的影响]。

Antibiotiki Pub Date : 1984-06-01
L M Vil'ner, V A Lashkevich
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引用次数: 0

摘要

在细胞培养和小鼠实验中,研究了病毒唑对poly(G) X poly(C)、poly(G, A) X poly(C)和poly(G, I) X poly(C)抗病毒活性的影响。结果表明,在鸡胚细胞培养物中,当病毒唑的浓度不足以显著抑制水疱性口炎病毒或辛德比病毒的发展时,病毒唑的抗病毒作用显著增强,并使合成的多核糖核苷酸复合物对上述病毒的最小有效剂量降低。在小鼠感染蜱传脑炎病毒1-2小时或24小时后联合给予poly (G) X poly (C)和病毒唑,比单独使用干扰素更能显著降低动物的死亡率。病毒唑本身活性不强,对聚(G) X聚(C)促进干扰素生成的强度没有显著影响。本文讨论了聚核糖核苷酸干扰素与病毒唑或其他具有广泛抗病毒谱的化疗药物联合成功治疗病毒感染的可能性。
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[Effect of virazole on the antiviral activity of poly(G) X poly(C) and other polyribonucleotide interferonogens].

The effect of virazole on the antiviral activity of poly (G) X poly (C), poly (G, A) X X poly (C) and poly(G, I) X poly (C) was studied in cell cultures and on mice. It was shown that virazole in concentrations not sufficient for significant inhibition of the development of vesicular stomatitis virus or Sindbis virus in chick embryo cell cultures markedly increased the antiviral effect and allowed decreasing the minimum effective doses of the synthetic polyribonucleotide complexes with respect to the above viruses. Combined administration of poly (G) X poly (C) and virazole to mice 1-2 or 24 hours after infection with tick-borne encephalitis virus provided a much more pronounced decrease in the death rate of the animals than the use of the interferonogen alone. Virazole per se was little active and had no significant effect on the intensity of interferonogenesis promoted by the use of poly (G) X poly (C). A possibility of successful therapy of viral infections with polyribonucleotide interferonogens in combination with virazole or other chemotherapeutic drugs with broad antiviral spectrum is discussed.

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