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作 者:何健民[1] 李晓眠[1] 刘民[1] 李电东[2] 刘琼岩[2]
机构地区:[1]天津医科大学微生物学教研室,300070 [2]中国协和医科大学中国医学科学院医药生物技术研究所
出 处:《天津医科大学学报》2001年第2期151-153,共3页Journal of Tianjin Medical University
基 金:国家自然科学基金课题部分项目 (编号 :39670019)
摘 要:目的 :体外测定抗生素S632A3 抗肠道病毒及单纯疱疹病毒I型的作用 ,为筛选新型抗病毒药物提供参考依据。方法 :用不同稀释度的抗生素S632A3 抑制3种肠道病毒及单纯疱疹病毒I型对Vero细胞的感染作用 ,48h后观察细胞病变效应 ,并用MTT法测定细胞活性。结果 :抗生素S632A3 能明显抑制肠道病毒及疱疹病毒对Vero细胞的致病变作用 ,使细胞存活率升高。结论 :该药物有较显著的抗肠道病毒及单纯疱疹病毒I型的作用 ,且对细胞的毒性很低 ,是一种具有潜在开发前景的药物。Objective: To assay the inhibitory effects of antibiotic S 632A 3 on enterovirus and herpes simplex type-1 virus(HSV-1) in vitro in order to select a new kind of antiviral drug. Methods: Vero cells were infected by different enteroviruses and were cultured with serial dilutions of S 632A 3.The inhibitory effects of S 632A 3 were evaluated with cell survival rates by MTT method and CPE.Results: The cytopathogenic effects (CPE)of cells infected by enterovirus or HSV-1 were inhibited significantly, resulting in higher cell survival rates. Conclusion:The results have shown that S 632A 3 had obviously enterovirus-inhibitory efficacy and low cytotoxity,therefore,it may become a potential candidate in drug development and deserves further research on animal experiments and antiviral mechanisms.
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