[胃芬津的遗传毒性和致癌潜力]。

E Mirkova
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引用次数: 0

摘要

保加利亚药物天麻素的遗传毒性是通过两种遗传毒性试验——"体外"沙门氏菌/突变试验和"体内"啮齿动物骨髓微核试验来研究的。胃杆菌素水溶液对“体外”沙门氏菌的致突变性——鼠骨髓微核试验。研究了胃杆菌素水溶液在不含或存在代谢激活(+/- S9)的情况下对5株组氨酸营养不良突变株——TA 1535、TA 1537、TA 1538、TA 98和TA 100的体外诱变性。在沙门氏菌/突变试验中,胃毒杆菌素在两个试验系列(+/- S9)的测试浓度范围内均未引起致突变反应。单次口服236 mg中心点kg-1 (80% DL50口服,小鼠)和118 mg中心点kg-1 (40% DL50口服,小鼠)后24、48和72小时,胃毒素对雄性C57Bl6小鼠骨髓细胞无微核诱导作用。在此基础上,得出了胃杆菌素无致突变性和致癌性的结论。
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[The genotoxicity and carcinogenic potential of gastrofenzin].

Genotoxicity of the Bulgarian drug gastrophensin was studied by using a battery of two genotoxicity assays "in vitro" - Salmonella/mutation assay and "in vivo" - the rodent bone marrow micronucleus test. Mutagenicity of water solution of gastrophensin towards Salmonella "in vitro" - the rodent bone marrow micronucleus test. Mutagenicity of water solution of gastrophensin towards Salmonella "in vitro" was tested in five mutant, histidine auxotrophic strains - TA 1535, TA 1537, TA 1538, TA 98 and TA 100 without and in the presence of metabolic activation (+/- S9) at concentration of 0.4, 2 and 10 mg center dot ml-1. Gastrophensin did not induce mutagenic response in the Salmonella/mutation assay in a range of tested concentrations in both series of assays (+/- S9). Gastrophensin did not induce micronuclei in bone marrow cells of male C57Bl6 mice at 24, 48 and 72 hours after single oral treatment with 236 mg center dot kg-1 (80% DL50 oral, mice) and 118 mg center dot kg-1 (40% DL50 oral, mice). Based on the present data a conclusion of the lack of mutagenicity and of carcinogenic potency of gastrophensin was made.

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