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口服给予怀孕小鼠和雄性小鼠红色食用色素所诱导的DNA损伤。

DNA damage induced by red food dyes orally administered to pregnant and male mice.

作者信息

Tsuda S, Murakami M, Matsusaka N, Kano K, Taniguchi K, Sasaki Y F

机构信息

Laboratory of Veterinary Public Health, Department of Veterinary Medicine, Faculty of Agriculture, Iwate University, Ueda 3-18-8, Morioka, Iwate 020-8550, Japan.

出版信息

Toxicol Sci. 2001 May;61(1):92-9. doi: 10.1093/toxsci/61.1.92.

Abstract

We determined the genotoxicity of synthetic red tar dyes currently used as food color additives in many countries, including JAPAN: For the preliminary assessment, we treated groups of 4 pregnant mice (gestational day 11) once orally at the limit dose (2000 mg/kg) of amaranth (food red No. 2), allura red (food red No. 40), or acid red (food red No. 106), and we sampled brain, lung, liver, kidney, glandular stomach, colon, urinary bladder, and embryo 3, 6, and 24 h after treatment. We used the comet (alkaline single cell gel electrophoresis) assay to measure DNA damage. The assay was positive in the colon 3 h after the administration of amaranth and allura red and weakly positive in the lung 6 h after the administration of amaranth. Acid red did not induce DNA damage in any sample at any sampling time. None of the dyes damaged DNA in other organs or the embryo. We then tested male mice with amaranth, allura red, and a related color additive, new coccine (food red No. 18). The 3 dyes induced DNA damage in the colon starting at 10 mg/kg. Twenty ml/kg of soaking liquid from commercial red ginger pickles, which contained 6.5 mg/10 ml of new coccine, induced DNA damage in colon, glandular stomach, and bladder. The potencies were compared to those of other rodent carcinogens. The rodent hepatocarcinogen p-dimethylaminoazobenzene induced colon DNA damage at 1 mg/kg, whereas it damaged liver DNA only at 500 mg/kg. Although 1 mg/kg of N-nitrosodimethylamine induced DNA damage in liver and bladder, it did not induce colon DNA damage. N-nitrosodiethylamine at 14 mg/kg did not induce DNA damage in any organs examined. Because the 3 azo additives we examined induced colon DNA damage at a very low dose, more extensive assessment of azo additives is warranted.

摘要

我们测定了目前在包括日本在内的许多国家用作食品色素添加剂的合成红焦油染料的遗传毒性

为进行初步评估,我们给4组妊娠小鼠(妊娠第11天)一次性口服苋菜红(食用红色素2号)、诱惑红(食用红色素40号)或酸性红(食用红色素106号)的极限剂量(2000毫克/千克),并在处理后3小时、6小时和24小时采集脑、肺、肝、肾、腺胃、结肠、膀胱和胚胎样本。我们使用彗星试验(碱性单细胞凝胶电泳)来测量DNA损伤。在给予苋菜红和诱惑红后3小时,结肠中的试验呈阳性,给予苋菜红后6小时,肺中的试验呈弱阳性。酸性红在任何采样时间的任何样本中均未诱导DNA损伤。这些染料均未对其他器官或胚胎的DNA造成损伤。然后,我们用苋菜红、诱惑红和一种相关的色素添加剂新胭脂红(食用红色素18号)对雄性小鼠进行了测试。这3种染料在10毫克/千克时开始诱导结肠中的DNA损伤。含有6.5毫克/10毫升新胭脂红的市售红姜泡菜浸泡液20毫升/千克诱导结肠、腺胃和膀胱中的DNA损伤。将这些效力与其他啮齿动物致癌物的效力进行了比较。啮齿动物肝癌致癌物对二甲氨基偶氮苯在1毫克/千克时诱导结肠DNA损伤,而仅在500毫克/千克时损伤肝脏DNA。虽然1毫克/千克的N-亚硝基二甲胺诱导肝脏和膀胱中的DNA损伤,但未诱导结肠DNA损伤。14毫克/千克的N-亚硝基二乙胺在任何检测器官中均未诱导DNA损伤。由于我们检测的3种偶氮添加剂在非常低的剂量下就诱导结肠DNA损伤,因此有必要对偶氮添加剂进行更广泛的评估。

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