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新型组胺H2受体拮抗剂乙磺替丁(BL-5641)的诱变性评估:采用细菌回复突变试验和V79中国仓鼠细胞正向突变试验

Mutagenic evaluation of etintidine (BL-5641), a novel histamine H2-receptor antagonist, using reverse mutation tests in bacteria and forward mutation tests in V79 Chinese hamster cells.

作者信息

Ishida F, Kondo H, Fukushima M, Kamei T

出版信息

Mutat Res. 1987 Aug;188(4):301-6. doi: 10.1016/0165-1218(87)90006-1.

Abstract

The mutagenic effects of etintidine (BL-5641), a novel histamine H2-receptor antagonist, were assessed using mutation in Salmonella typhimurium, Escherichia coli, and V79 Chinese hamster cells (V79 cells). Etintidine did not increase the revertant colonies in the presence or absence of S9 mix at concentrations from 5 to 5000 micrograms/plate in either of the bacterial tester strains. Etintidine also did not increase 6-thioguanine- and ouabain-resistant colonies in V79 cells in the presence or absence of S9 mix even at 37% cellular survival concentration. There was no evidence that etintidine had any mutagenic activity in any of the tests.

摘要

使用鼠伤寒沙门氏菌、大肠杆菌和V79中国仓鼠细胞(V79细胞)中的突变来评估新型组胺H2受体拮抗剂乙溴替丁(BL-5641)的致突变作用。在两种细菌测试菌株中,当浓度为5至5000微克/平板时,无论有无S9混合物,乙溴替丁都不会增加回复菌落数。即使在37%细胞存活浓度下,无论有无S9混合物,乙溴替丁在V79细胞中也不会增加对6-硫代鸟嘌呤和哇巴因耐药的菌落数。没有证据表明乙溴替丁在任何测试中具有任何致突变活性。

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