苦参酚类组分对Ames实验致突变性的调节作用。

K. Kaur, Saroj Arora, Subodh Kumar, A. Nagpal
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引用次数: 14

摘要

在鼠伤寒沙门菌TA98和TA100试验菌株中,测定了沙麻酚类组分(可溶于氯仿和不溶于氯仿)对4-硝基-邻苯二胺(NPD)和叠氮化钠两种直接作用诱变剂以及对s9依赖性诱变剂2-氨基芴(2AF)的抗诱变作用。结果表明,与直接作用诱变剂相比,黄叶参酚类组分对s9依赖性诱变剂诱导的反复性抑制作用更显著。此外,在2AF诱导突变的预处理模式下,酚类组分分别表现出98%和101.55%的最大抑制作用。总的来说,这些组分比直接作用诱变剂更有效地抑制s9依赖性诱变剂诱导的逆转录。孵育前的抑制率高于直接作用诱变剂。不溶于氯仿的部位比溶于氯仿的部位具有更强的抑制作用,说明不溶于氯仿的部位比溶于氯仿的部位多酚含量高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulatory effect of phenolic fractions of Terminalia arjuna on the mutagenicity in Ames assay.
We determined the antimutagenicity of phenolic fractions of Terminalia arjuna (soluble and insoluble in chloroform) against two direct-acting mutagens, 4-nitro-o-phenylenediamine (NPD) and sodium azide, and against the S9-dependent mutagen 2-aminofluorene (2AF), in TA98 and TA100 tester strains of Salmonella typhimurium. We found that the phenolic fractions of T. arjuna inhibited revertants induced by the S9-dependent mutagen more remarkably than the direct-acting mutagens. Furthermore, the phenolic fractions showed maximum inhibition of 98% and 101.55%, respectively, in the pre-incubation mode of treatment against the mutations induced by 2AF. Overall, the fractions inhibited the revertants induced by S9-dependent mutagens more effectively than those induced by direct-acting mutagens. The percentage of inhibition was higher in the pre-incubation than with direct acting mutagens. The fraction insoluble in chloroform showed more inhibition than the soluble one, which corresponds to a higher polyphenol content in the insoluble fraction than in the soluble extract.
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