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使用体内/体外大鼠肝脏DNA修复试验来预测3种新型偶氮诱变剂的相对啮齿动物肝癌致癌潜力。

Use of an in vivo/in vitro rat liver DNA repair assay to predict the relative rodent hepatocarcinogenic potency of 3 new azo mutagens.

作者信息

Beije B, Ashby J

出版信息

Carcinogenesis. 1985 Apr;6(4):611-5. doi: 10.1093/carcin/6.4.611.

Abstract

The in vivo/in vitro rat liver DNA repair assay described by Mirsalis and Butterworth has been employed to compare the relative genotoxicity to the rat liver of three mutagenic analogues of the potent rat hepatocarcinogen 6-dimethylamino-phenylazobenzthiazole (6BT). The compounds evaluated were 6BT, its monomethyl analogue (6-monomethylamino-phenylazobenzthiazole; MA6BT), an analogue in which the -NMe2 group of 6BT is replaced by a piperidinyl group (6-[4-N-piperidinylphenyl]azobenzene; 6PT) and the N-cyanoethyl analogue of MA6BT (6-[p-(N-beta-cyanoethyl-N-methylamino)-phenylazo]benzthiazole; CNEt6BT). The order of relative carcinogenic potency predicted by the Salmonella mutation data was CNEt6BT much greater than MA6BT = 6BT much greater than 6PT. In contrast, that inferred from the in vivo liver DNA repair data was MA6BT greater than 6BT much greater than CNEt6BT much greater than 6PT. This divergence of predictions is discussed in terms of the differing solution properties of the four test chemicals.

摘要

米尔萨利斯(Mirsalis)和巴特沃思(Butterworth)所描述的体内/体外大鼠肝脏DNA修复试验,已被用于比较三种诱变类似物对大鼠肝脏的相对遗传毒性,这三种类似物是强效大鼠致癌物6-二甲基氨基苯基偶氮苯并噻唑(6BT)的类似物。所评估的化合物为6BT、其单甲基类似物(6-单甲基氨基苯基偶氮苯并噻唑;MA6BT)、一种6BT的-NMe2基团被哌啶基取代的类似物(6-[4-N-哌啶基苯基]偶氮苯;6PT)以及MA6BT的N-氰基乙基类似物(6-[对-(N-β-氰基乙基-N-甲基氨基)-苯基偶氮]苯并噻唑;CNEt6BT)。沙门氏菌突变数据预测的相对致癌效力顺序为CNEt6BT远大于MA6BT = 6BT远大于6PT。相比之下,从体内肝脏DNA修复数据推断出的顺序为MA6BT大于6BT远大于CNEt6BT远大于6PT。根据四种受试化学品不同的溶液性质,对这种预测差异进行了讨论。

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