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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Evaluation of the antigenotoxic potential of monomeric and dimeric flavanols, and black tea polyphenols against heterocyclic amine-induced DNA damage in human lymphocytes using the Comet assay.
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Evaluation of the antigenotoxic potential of monomeric and dimeric flavanols, and black tea polyphenols against heterocyclic amine-induced DNA damage in human lymphocytes using the Comet assay.

机译:使用彗星分析评估单体和二聚体黄烷醇以及红茶多酚对杂环胺诱导的人类淋巴细胞DNA损伤的抗原毒性潜力。

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摘要

The polyphenolic dimers, epicatechin-4beta-8-catechin (B1), epicatechin-4beta-8-epicatechin (B2), catechin-4beta-8-catechin (B3), catechin-4beta-8-epicatechin (B4), and the gallate ester epicatechin-4beta-8-epicatechin gallate (B'2G) were isolated from grape seeds, and theaflavins and theafulvins from black tea brews. The ability of these naturally-occurring polyphenols to afford protection against the genotoxicity of the heterocyclic amine 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) was compared with that of the monomeric tea flavanols, (+)-catechin (C), (-)-epicatechin (EC), (-)-epicatechin gallate (ECG), (-)-epigallocatechin (EGC) and (-)-epigallocatechin gallate (EGCG). Genotoxic activity was evaluated in human peripheral lymphocytes using the Comet assay. At the concentration range of 1-100 microM, neither the monomeric nor the dimeric flavanols prevented the lymphocyte DNA damage induced by Trp-P-2. In contrast, both of the black tea polyphenols, theafulvins and theaflavins, at a dose range of 0.1-0.5 mg/ml, prevented, in a concentration-dependent manner, the DNA damage elicited by Trp-P-2. Finally, neither the monomeric and dimeric polyphenols (100 microM) nor the theafulvins and theaflavins (0.5mg/ml) caused any DNA damage in the human lymphocytes. These studies illustrate that black tea theafulvins and theaflavins, if absorbed intact, may contribute to the anticarcinogenic potential associated with black tea intake.
机译:多酚二聚体,表儿茶素4beta-8-儿茶素(B1),表儿茶素4beta-8-表儿茶素(B2),儿茶素4beta-8-儿茶素(B3),儿茶素4beta-8-表儿茶素(B4)和没食子酸酯表儿茶素-4β-8-表儿茶素没食子酸酯(B'2G)是从葡萄籽中分离得到的,茶黄素和茶黄素是从红茶中提取的。比较了这些天然存在的多酚提供的抗杂环胺3-氨基-1-甲基-5H-吡啶并[4,3-b]吲哚(Trp-P-2)遗传毒性的能力。单体茶黄烷醇,(+)-儿茶素(C),(-)-表儿茶素(EC),(-)-表儿茶素没食子酸酯(ECG),(-)-表没食子儿茶素(EGC)和(-)-表没食子儿茶素没食子酸酯(EGCG) 。使用Comet分析法评估人外周血淋巴细胞的基因毒性活性。在1-100 microM的浓度范围内,单体黄烷醇和二聚体黄烷醇均不能阻止Trp-P-2诱导的淋巴细胞DNA损伤。相反,剂量范围为0.1-0.5 mg / ml的红茶多酚茶碱和茶黄素均以浓度依赖性的方式防止了Trp-P-2引起的DNA损伤。最后,单体和二聚体多酚(100 microM)或茶黄素和茶黄素(0.5mg / ml)都不会对人类淋巴细胞造成DNA损伤。这些研究表明,红茶茶黄素和茶黄素如果被完整吸收,可能有助于与红茶摄入相关的抗癌作用。

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