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偶氮类食品添加剂诱导大鼠和小鼠结肠 DNA 损伤的差异。

Differential colon DNA damage induced by azo food additives between rats and mice.

机构信息

Laboratory of Veterinary Public Health, Department of Veterinary Medicine, Iwate University, Morioka, Japan.

出版信息

J Toxicol Sci. 2010 Aug;35(4):547-54. doi: 10.2131/jts.35.547.

Abstract

Azo dyes, amaranth, allura red and new coccine, which are currently used as food color additives in Japan, have been reported to cause colon specific DNA damage in mice. To examine species difference in the DNA damage between rats and mice, each of dyes was administered to male mice (1 and 10 mg/kg) and male rats (10, 100 and 1,000 mg/kg) by gavage. Brain, lung, liver, kidney, glandular stomach, colon, urinary bladder and bone marrow were sampled 3 hr (for mice) and 3, 6, 12 and 24 hr (for rats) after the treatment. The alkaline comet assay showed DNA damage in the mouse colon 3 hr after the administration of all of the dyes at 10 mg/kg. In rats, however, none of the dyes damaged DNA. Azo dyes should undergo metabolic reduction in the colon to be adducted to DNA. To determine transit time of the dyes to the colon after their administration, gastric emptying and intestinal transport in mice and rats were examined using brilliant blue FCF (BB) as an indicator. The half times of gastric emptying were 70 and 80 min for mice and rats, respectively; and about 60% of the BB was removed from the stomach 1 hr after the gastric intubation in both mice and rats. BB reached the mouse and rat colon 1 and 3 hr after the administration, respectively. Considering the wide dose range and sampling times well covering the transit time to the colon, rats may be insensitive to these azo dye-induced DNA damage.

摘要

偶氮染料、苋菜红、诱惑红和新红,这些目前在日本被用作食品着色添加剂,据报道会引起小鼠结肠特异性 DNA 损伤。为了研究大鼠和小鼠之间 DNA 损伤的种属差异,将这些染料分别以 1 和 10mg/kg 剂量经灌胃给予雄性小鼠,以 10、100 和 1000mg/kg 剂量经灌胃给予雄性大鼠。在染毒后 3 小时(用于小鼠)和 3、6、12 和 24 小时(用于大鼠),采集脑、肺、肝、肾、胃腺、结肠、膀胱和骨髓。碱性彗星试验显示,在 10mg/kg 剂量下,所有染料在染毒后 3 小时均可引起小鼠结肠 DNA 损伤。然而,在大鼠中,没有一种染料可引起 DNA 损伤。偶氮染料应该在结肠中进行代谢还原,然后与 DNA 结合。为了确定染料在给药后到达结肠的转运时间,使用亮蓝 FCF(BB)作为指示剂,分别检测了小鼠和大鼠的胃排空和肠道传输。胃排空的半衰期分别为 70 和 80 分钟;在胃内灌胃 1 小时后,小鼠和大鼠胃中的 BB 约有 60%被清除。BB 在给药后 1 小时和 3 小时分别到达小鼠和大鼠的结肠。考虑到剂量范围广泛,采样时间很好地覆盖了到达结肠的转运时间,大鼠可能对这些偶氮染料诱导的 DNA 损伤不敏感。

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