膳食纤维对大鼠组织DNA加合物形成的影响。

P Goldin-Lang, G Dongowski, H J Zunft
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摘要

研究了不同微生物状态和不同饮食(含或不含不同程度酯化(DE)果胶)的大鼠组织样本中dna加合物样本地化合物(i -化合物)的发生。21 d后,每组6只无菌大鼠和10只常规大鼠分别饲喂无果胶或添加7.5%的3种不同酯化果胶制剂(果胶A: DE: 92.6%;果胶B: DE 70.8%;果胶C: DE 34.5%)。从结肠粘膜、肝、肺、肾中分离DNA,采用高灵敏度32P后标记法进行DNA加合物分析。在饲喂低酯化果胶c的无菌动物中,在所有组织样本中均检测到i -化合物。在高酯化果胶A和B下,仅在肝脏中可见弱加合物形成,而在结肠粘膜、肺和肾脏中没有。在传统动物DNA加合物被发现在所有的样品强度最高的结肠粘膜在对照组,其次是low-esterified果胶C组,和弱强度下higher-esterified果胶a和b实验表明倾向于一个更高的点的数量和强度无菌的与传统的老鼠相比,在老鼠pectin-free与果胶的饮食相比,和下low-esterified相比higher-esterified果胶。
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Influence of dietary fiber on DNA adduct formation in rat tissues.

The occurrence of DNA-adduct-like indigenous compounds (I-compounds) was examined in tissue samples of rats differing in their microbial state and diet with or without pectins of different degrees of esterification (DE). For 21 days groups of six germfree and ten conventional rats were each fed either pectin-free or with diets containing 7.5% of three differently esterified pectin preparations (pectin A: DE 92.6%; pectin B: DE 70.8%; pectin C: DE 34.5%). DNA was isolated from colonic mucosa, liver, lung, kidney and measured by the highly sensitive 32P postlabelling assay for DNA adduct analysis. In germfree animals I-compounds were detected in all tissue samples after feeding the low-esterified pectin C. Under the higher-esterified pectins, A and B, a weak adduct formation could be demonstrated only in the liver, but not in the colonic mucosa, lung, and kidney. In conventional animals DNA adducts were found in all samples of colonic mucosa with the highest intensity in the control group, followed by the low-esterified pectin C group, and a weak intensity under the higher-esterified pectins A and B. The experiments show a tendency to a higher number and intensity of spots in the germfree compared with the conventional rats, in rats with a pectin-free compared with the pectin diet, and under the low-esterified compared with the higher-esterified pectins.

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