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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Suppressive effects of retinoids, carotenoids and antioxidant vitamins on heterocyclic amine-induced umu C gene expression in Salmonella typhimurium (TA 1535/pSK 1002).
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Suppressive effects of retinoids, carotenoids and antioxidant vitamins on heterocyclic amine-induced umu C gene expression in Salmonella typhimurium (TA 1535/pSK 1002).

机译:维甲酸,类胡萝卜素和抗氧化剂维生素对鼠伤寒沙门氏菌中杂环胺诱导的umu C基因表达的抑制作用(TA 1535 / pSK 1002)。

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摘要

Effects of retinoids, carotenoids and antioxidant vitamins were studied by mutagen-induced umu C gene expression system in Salmonella typhimurium (TA 1535/pSK 1002). Retinol (vitamin A), retinol acetate and retinoic acid showed remarkable inhibitory activities, whereas retinol palmitate exhibited significant but weak activity for umu C gene expression in tester bacteria induced by 3-amino-3,4-dimethyl-5H-pyrido[4.3-b]indol (Trp-P-1) in the presence of hepatic metabolizing enzymes (S9 mixture). Carotenoids having provitamin A activity (beta-carotene and canthaxanthin) exhibited moderate suppressive effects on the same experimental system. The ranks of suppressive activities were retinol > retinol acetate > retinoic acid > canthaxanthin > beta-carotene > retinol palmitate and their doses for inhibition by 50% (ID50) were estimated to be 1.2 x 10(-7), 3.0 x 10(-7), 5.4 x 10(-7), 1.5 x 10(-6), 4.0 x 10(-5) and 6.0 x 10(-5) M, respectively. However, they did not cause significant inhibition on umu C gene expression induced by direct-acting mutagen (adriamycin or mitomycin C) in the absence of S9 mixture. Inhibition of umu gene expression appears to be due to inhibition of P450-mediated metabolic activation of the heterocyclic amine Trp-P-1. Ascorbic acid (vitamin C) showed weak but significant suppressive activity at high-dose concentrations (3 x 10(-6) - 10(-4)M). However, alpha-tocopherol did not exhibit significant suppression at all dose concentrations. The significance of the experimental results is discussed from the viewpoint of the chemoprevention against genotoxicity associated with carcinogenesis.
机译:通过诱变诱导的鼠伤寒沙门氏菌的umu C基因表达系统研究了类维生素A,类胡萝卜素和抗氧化剂维生素的作用(TA 1535 / pSK 1002)。视黄醇(维生素A),乙酸视黄醇和视黄酸显示出显着的抑制活性,而棕榈酸视黄醇对3-氨基-3,4-二甲基-5H-吡啶诱导的细菌中的umu C基因表达表现出显着但弱的活性[4.3- b]吲哚(Trp-P-1)在存在肝代谢酶(S9混合物)的情况下。具有维生素原A活性的类胡萝卜素(β-胡萝卜素和角黄素)在相同的实验系统上表现出中等抑制作用。抑制活性的等级是视黄醇>乙酸视黄醇>维甲酸>角黄素>β-胡萝卜素>视黄醇棕榈酸酯,其抑制50%(ID50)的剂量估计为1.2 x 10(-7),3.0 x 10(- 7),5.4 x 10(-7),1.5 x 10(-6),4.0 x 10(-5)和6.0 x 10(-5)M。但是,在不存在S9混合物的情况下,它们不会对直接作用诱变剂(阿霉素或丝裂霉素C)诱导的umu C基因表达产生显着抑制作用。 umu基因表达的抑制似乎是由于抑制了P450介导的杂环胺Trp-P-1的代谢活化。抗坏血酸(维生素C)在高剂量浓度(3 x 10(-6)-10(-4)M)下显示出弱但显着的抑制活性。但是,α-生育酚在所有剂量浓度下均未表现出明显的抑制作用。从化学预防针对与致癌相关的基因毒性的角度讨论了实验结果的重要性。

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