Ip C
Department of Breast Surgery, Roswell Park Memorial Institute, Buffalo, NY 14263.
J Natl Cancer Inst. 1988 Apr 20;80(4):258-62. doi: 10.1093/jnci/80.4.258.
The influence of a low methionine intake on the chemopreventive efficacy of selenomethionine versus selenite was compared in the 7,12-dimethylbenz[a]anthracene-induced mammary tumor model in rats. Animals were fed from weaning a purified 20% casein diet with or without 0.3% methionine supplementation. Selenomethionine or selenite, at a final concentration of 3 ppm of selenium (Se), was added to the diet starting 5 days after DMBA administration. Control rats continued to receive the basal diets which contained 0.1 ppm of Se. Results of the carcinogenesis experiment indicated that suboptimal dietary methionine significantly reduced the protective effect of selenomethionine in cancer prevention. In contrast, the efficacy of selenite was not affected. In rats given 3 ppm of selenomethionine, tissue Se was actually higher in those fed a diet with a suboptimal amount of methionine than in those with an adequate intake of methionine. On the other hand, dietary methionine did not influence the level of tissue Se in animals given selenite. An increase of dietary methionine to 0.6% did not enhance the efficacy of selenomethionine in cancer protection but would allow the use of a higher level of selenite without the accompanying adverse effects. The biological significance of Se utilization under suboptimal or adequate methionine intake was also assessed using the glutathione peroxidase assay in the liver of Se-deficient rats given graded levels of Se as either selenite or selenomethionine. The enzyme study demonstrated that low dietary methionine decreased the nutritional biopotency of selenomethionine in restoring glutathione peroxidase activity but not that of selenite. These experiments suggest that adequate methionine intake is required for the utilization of selenomethionine for nutritional and anticarcinogenic purposes.
在7,12-二甲基苯并[a]蒽诱导的大鼠乳腺肿瘤模型中,比较了低蛋氨酸摄入量对硒代蛋氨酸与亚硒酸盐化学预防效果的影响。从断奶开始,给动物喂食添加或不添加0.3%蛋氨酸的纯化20%酪蛋白饮食。在给予DMBA后5天开始,将最终浓度为3 ppm硒(Se)的硒代蛋氨酸或亚硒酸盐添加到饮食中。对照大鼠继续接受含0.1 ppm Se的基础饮食。致癌实验结果表明,饮食中蛋氨酸不足会显著降低硒代蛋氨酸在癌症预防中的保护作用。相比之下,亚硒酸盐的效果不受影响。在给予3 ppm硒代蛋氨酸的大鼠中,摄入蛋氨酸不足的大鼠组织硒含量实际上高于蛋氨酸摄入充足的大鼠。另一方面,饮食中的蛋氨酸对给予亚硒酸盐的动物组织硒水平没有影响。将饮食中蛋氨酸增加到0.6%并不会增强硒代蛋氨酸在癌症保护中的效果,但可以使用更高水平的亚硒酸盐而不会产生伴随的不良反应。还通过在给予不同水平硒(以亚硒酸盐或硒代蛋氨酸形式)的缺硒大鼠肝脏中进行谷胱甘肽过氧化物酶测定来评估蛋氨酸摄入不足或充足时硒利用的生物学意义。酶研究表明,低饮食蛋氨酸会降低硒代蛋氨酸在恢复谷胱甘肽过氧化物酶活性方面的营养生物效能,但不会降低亚硒酸盐的效能。这些实验表明,为了将硒代蛋氨酸用于营养和抗癌目的,需要摄入充足的蛋氨酸。