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Effects of Tea and Chlorophyllin on the Mutagenicity of N-Hydroxy-IQ: Studies of Enzyme Inhibition Molecular Complex Formation and Degradation/Scavenging of the Active Metabolites

机译:茶和叶绿素对N-羟基-IQ致突变性的影响:酶抑制分子复合物形成和活性代谢产物的降解/清除的研究

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摘要

Green tea and black tea inhibit the formation of carcinogen-DNA adducts and colonic aberrant crypts in rats given 2-amino-3-methylimidazo[4, 5-f]quinoline (IQ), a mutagen from cooked meat. The Salmonella mutagenicity assay was used in the present study to test individual constituents of tea as inhibitors of 2-hydroxyamino-3-methylimidazo[4, 5-f]quinoline (N-hydroxy-IQ), a direct-acting metabolite of IQ. Testing of pure compounds at doses relevant to their levels in tea identified epigallocatechin (EGC) and epigallocatechin-3-gallate (EGCG) as the primary antimutagens. Studies of the inhibitory mechanisms established that the rate of degradation of N-hydroxy-IQ under aqueous conditions was not increased significantly in the presence of tea, in contrast to the results obtained with the complexing agent chlorophyllin (CHL), which rapidly degraded the mutagen. Interaction between N-hydroxy-IQ and several tea constituents was detected in spectro-photometric studies, but the binding constants were only on the order of 1 × 103 M−1, suggesting that mechanisms other than complex formation might prevail under the conditions of the Salmonella assay. Comparison of the results in two different strains of Salmonella typhimurium, TA98 and TA98/1,8-DNP6, indicated that the antimutagenic activity of EGCG was dependent, at least in part, on a functional O-acetyltransferase activity in the bacteria. These studies suggest that tea constituents inhibit the enzyme(s) which generate the aryl nitrenium ion and directly scavenge the reactive electrophile, whereas CHL complexes with heterocyclic amines and facilitates the degradation of active metabolites.
机译:绿茶和红茶会抑制2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ)(一种来自熟肉的诱变剂),从而抑制致癌物-DNA加合物和结肠异常隐窝的形成。本研究中使用沙门氏菌诱变性试验来测试茶的各个成分,作为2-羟基氨基-3-甲基咪唑并[4,5-f]喹啉(N-羟基-IQ)(一种IQ的直接作用代谢物)的抑制剂。对茶中与化合物含量相关的剂量的纯化合物的测试确定了表没食子儿茶素(EGC)和表没食子儿茶素3-没食子酸酯(EGCG)是主要的抗突变体。抑制机制的研究表明,在茶水存在下,在水性条件下N-羟基-IQ的降解速率没有显着提高,这与络合剂叶绿素(CHL)所获得的结果相反,后者能够快速降解诱变剂。分光光度法研究了N-羟基-IQ与几种茶成分之间的相互作用,但结合常数仅为1×10 3 M -1 ,表明在沙门氏菌测定条件下,除了复合物形成以外的其他机制可能占主导。比较两种鼠伤寒沙门氏菌菌株TA98和TA98 / 1,8-DNP6中的结果,表明EGCG的抗诱变活性至少部分取决于细菌中的功能性O-乙酰转移酶活性。这些研究表明,茶成分会抑制产生芳基氮离子的酶,并直接清除反应性亲电试剂,而CHL与杂环胺络合并促进活性代谢物的降解。

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