Modulatory effect of phenolic fractions of Terminalia arjuna on the mutagenicity in Ames assay.

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

Abstract

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.
苦参酚类组分对Ames实验致突变性的调节作用。
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。
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