首页> 外文期刊>Environmental research >In utero exposure to perfluorooctanoate (PFOA) or perfluorooctane sulfonate (PFOS) did not increase body weight or intestinal tumorigenesis in multiple intestinal neoplasia (Min/+) mice
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In utero exposure to perfluorooctanoate (PFOA) or perfluorooctane sulfonate (PFOS) did not increase body weight or intestinal tumorigenesis in multiple intestinal neoplasia (Min/+) mice

机译:在子宫内暴露于全氟辛酸(PFOA)或全氟辛烷磺酸(PFOS)不会增加多肠新生(Min / +)小鼠的体重或肠肿瘤发生

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摘要

We examined whether perfluorooctanoate (PFOA) or perfluorooctane sulfonate (PFOS) had obesogenic effects and if they increased spontaneous intestinal tumorigenesis in the mouse model C57BL/6J-Min/+ (multiple intestinal neoplasia) after in utero exposure. The dams were exposed to PFOA or PFOS (0.01, 0.1 or 3.0 mg/kg bw/day) by po gavage on GD1-17. The Min/+ and wild-type offspring were terminated at week 11 for examination of intestinal tumorigenesis or at week 20 for obesogenic effect, respectively. Body weights of the dams and pups were recorded throughout life. Food intake was determined at week 6 and 10. Blood glucose (non-fasted) was measured at week 6 and 11. No obesogenic effect of PFOA or PFOS was observed up to 20 weeks of age. PFOA or PFOS did not increase the incidence or number of tumors in the small intestine or colon of the Min/+ mice or affect their location along the intestines. Feed intake was not affected. There were some indications of toxicity of PFOA, but not of PFOS. There was lower survival of pups after 3.0 mg/kg PFOA, lower body weight in pups after 3.0 and possibly 0.1 mg/kg PFOA, and increased relative liver weight after 0.01 and possibly 0.1 mg/kg PFOA. Plasma glucose was lower after 0.01 and 0.1 mg/kg PFOA. In conclusion, exposure to PFOA and PFOS in utero with the doses used did not have obesogenic effect on either Min/+ or wild-type mice, at least not up to 11 or 20 weeks of age, nor increased intestinal tumorigenesis in Min/+ mice.
机译:我们检查了全氟辛酸酯(PFOA)或全氟辛烷磺酸(PFOS)是否具有致肥胖作用,以及它们是否在子宫内暴露后在小鼠模型C57BL / 6J-Min / +(多发性肠肿瘤)中增加了自发性肠肿瘤的发生。通过在GD1-17上进行强饲法将水坝暴露于PFOA或PFOS(0.01、0.1或3.0 mg / kg bw /天)。 Min / +和野生型后代分别在第11周终止以检查肠道肿瘤发生或在第20周终止致肥胖作用。在整个生命中记录水坝和幼崽的体重。在第6周和第10周确定食物摄入量。在第6周和第11周测量血糖(非禁食)。直至20周龄,未观察到PFOA或PFOS的致肥胖作用。 PFOA或PFOS不会增加Min / +小鼠小肠或结肠中肿瘤的发生率或数量,也不影响其在肠中的位置。采食量不受影响。有一些迹象表明全氟辛烷磺酸具有毒性,而全氟辛烷磺酸则无。 3.0 mg / kg PFOA后幼崽的存活率较低,3.0和0.1mg / kg PFOA后幼崽的体重较低,而0.01和0.1mg / kg PFOA后相对肝重增加。 0.01和0.1 mg / kg PFOA后,血浆葡萄糖降低。总之,子宫内暴露于PFOA和PFOS的剂量对Min / +或野生型小鼠没有致肥胖作用,至少不超过11​​或20周龄,Min / +的肠道肿瘤发生也没有增加老鼠。

著录项

  • 来源
    《Environmental research》 |2014年第7期|251-263|共13页
  • 作者单位

    Department of Food, Water and Cosmetics, Division of Environmental Medicine, Norwegian Institute of Public Health, P.O. Box 4404 Nydalen, NO-0403 Oslo, Norway;

    Department of Food, Water and Cosmetics, Division of Environmental Medicine, Norwegian Institute of Public Health, P.O. Box 4404 Nydalen, NO-0403 Oslo, Norway;

    Department of Exposure and Risk Assessment, Division of Environmental Medicine, Norwegian Institute of Public Health, NO-0403 Oslo, Norway;

    Department of Exposure and Risk Assessment, Division of Environmental Medicine, Norwegian Institute of Public Health, NO-0403 Oslo, Norway;

    Department of Food, Water and Cosmetics, Division of Environmental Medicine, Norwegian Institute of Public Health, P.O. Box 4404 Nydalen, NO-0403 Oslo, Norway;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Intestinal tumorigenesis; In utero exposure; Min/+ mouse; Obesogen; Perfluorooctane sulfonate; Perfluorooctanoate;

    机译:肠道肿瘤发生;宫内暴露;最小/ +鼠标;肥胖源全氟辛烷磺酸盐;全氟辛酸酯;

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