首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Mutagenic activation of an antischistosomal drug by enteric streptococcus sps in vitro and in vivo
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Mutagenic activation of an antischistosomal drug by enteric streptococcus sps in vitro and in vivo

机译:肠链球菌属植物在体外和体内对抗血吸虫药物的诱变激活

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AbstractPrevious studies have shown that a new antischistosomal drug, 4‐isothiocyano‐4′‐nitro diphenylamine (CGP 4540, amoscanate), is not mutagenic in vitro, but the urines of animals treated with this drug have mutagenic activity. Mutagenicity can be eliminated by coadministration of some antibacterial agents and is not demonstrable in germ‐free animals. The present study describes attempts to isolate and identify intestinal microorganisms responsible for the mutagenic activation of amoscanate. Streptococcus equinus, isolated from the intestinal tract of mice, as well as some other species of Streptococcus, were found to produce mutagenic activation of amoscanate when introduced into animals pretreated with antibacterial agents. Similarly, incubation of these strains with amoscanate in vitro resulted in the formation of a mutageni
机译:摘要 既往研究表明,一种新的抗血吸虫药物4-异硫氰基-4′-硝基二苯胺(CGP 4540,amoscanate)在体外不具有致突变性,但用该药物处理的动物尿液具有致突变活性。致突变性可以通过联合施用某些抗菌剂来消除,并且在无菌动物中无法证明。本研究描述了分离和鉴定负责阿莫斯卡酸盐诱变激活的肠道微生物的尝试。从小鼠肠道中分离出的马链球菌以及一些其他种类的链球菌被发现在引入用抗菌剂预处理的动物中时会产生氨苯酸的诱变激活。类似地,这些菌株在体外与阿莫斯卡酸盐孵育导致诱变剂的形成

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