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环己醇对鼠伤寒沙门氏菌TA100菌株中4-(N-亚硝基甲基氨基)-1-(3-吡啶基)-1-丁酮和N-亚硝基二乙胺的抗诱变性

Antimutagenicity of cyclohexanol towards 4-(N-nitrosomethylamino)-1-(3-pyridyl)-1-butanone and N-nitrosodiethylamine in Salmonella typhimurium strain TA100.

作者信息

Espinosa-Aguirre J J, Vilchis C, Ostrosky-Wegman P, Benitez L, Lares I, Rubio J

机构信息

Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, D.F.

出版信息

Mutat Res. 1993 Aug;300(3-4):151-4. doi: 10.1016/0165-1218(93)90046-g.

Abstract

The ability of cyclohexanol to inhibit the mutagenicity of tobacco-specific nitrosamine 4-(N-nitrosomethylamino)-1-(3-pyridyl)-1-butanone (NNK) and of N-nitrosodiethylamine (NDEA) was tested on Salmonella typhimurium strain TA100. Cyclohexanol produced a dose-dependent decrease in the number of revertants induced by a single dose of NNK (24 mumoles) or NDEA (59 mumoles). Nevertheless, this inhibitory effect was not observed with other premutagenic agents such as benzo[a]pyrene and 2-aminoanthracene nor with direct mutagens such as ethyl methanesulfonate and methyl methanesulfonate. These results suggest that cyclohexanol interferes with the 'bioactivation' of the tested nitrosamines in a similar way that other alcohols such as ethanol or isopropanol interfere with N-nitro-sodimethylamine and NDEA metabolism.

摘要

在鼠伤寒沙门氏菌TA100菌株上测试了环己醇抑制烟草特有的亚硝胺4-(N-亚硝基甲基氨基)-1-(3-吡啶基)-1-丁酮(NNK)和N-亚硝基二乙胺(NDEA)致突变性的能力。环己醇使单剂量NNK(24微摩尔)或NDEA(59微摩尔)诱导的回复突变菌落数呈剂量依赖性减少。然而,在用其他前诱变剂如苯并[a]芘和2-氨基蒽以及直接诱变剂如甲磺酸乙酯和甲磺酸甲酯处理时,未观察到这种抑制作用。这些结果表明,环己醇以类似于乙醇或异丙醇等其他醇类干扰N-亚硝基二甲胺和NDEA代谢的方式,干扰了所测试亚硝胺的“生物活化”。

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