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在用过量大豆和缺碘饮食处理的大鼠中,显著协同促进N-双(2-羟丙基)亚硝胺引发的甲状腺肿瘤发生。

Pronounced synergistic promotion of N-bis(2-hydroxypropyl)nitrosamine-initiated thyroid tumorigenesis in rats treated with excess soybean and iodine-deficient diets.

作者信息

Nishikawa Akiyoshi, Ikeda Takako, Son Hwa-Young, Okazaki Kazushi, Imazawa Takayoshi, Umemura Takashi, Kimura Shuichi, Hirose Masao

机构信息

Division of Pathology, National Institute of Health Sciences, Tokyo 158-8501, and Showa Women's University, Tokyo 154-8533, Japan.

出版信息

Toxicol Sci. 2005 Aug;86(2):258-63. doi: 10.1093/toxsci/kfi206. Epub 2005 May 18.

DOI:10.1093/toxsci/kfi206
PMID:15901912
Abstract

We have reported that excess soybean treatment and iodine deficiency synergistically interact, resulting in remarkable induction of thyroid hyperplasias in rats. In the present study, modifying effects of excess soybean and iodine-deficient diets were investigated in the post-initiation phase of N-bis(2-hydroxypropyl)nitrosamine [DHPN]-initiated thyroid tumorigenesis in rats. AIN-93G in which casein was replaced with gluten was used as a basal diet to avoid possible iodine contamination. In Experiment 1, F-344 rats of both sexes were sc injected with DHPN at a dose of 2800 mg/kg body weight and then fed a diet containing 0%, 0.8%, 4%, or 20% defatted soybean for 12 weeks, with proportional replacement of gluten by soybean flour. Although no thyroid proliferative lesions were found in any group, the absolute thyroid weights were significantly (p < 0.01) elevated with the 20% soybean treatment. In Experiment 2, after similar sc injection of DHPN, rats were fed a basal diet or a diet containing 20% soybean under iodine normal or deficient conditions for 12 weeks. Soybean feeding to both sexes under iodine deficient but not normal conditions dramatically enhanced the development of thyroid follicular adenomas (p < 0.01) and adenocarcinomas (p < 0.05), in good agreement with decrease in thyroxine and increase in thyroid-stimulating hormone. Thus co-exposure to excess soybean and iodine deficiency results in synergistic promotion of DHPN-initiated thyroid tumorigenesis in rats, of which mechanisms appear to primarily involve effects on serum hormone levels.

摘要

我们曾报道,过量大豆处理与碘缺乏存在协同作用,可导致大鼠甲状腺增生显著增加。在本研究中,我们调查了过量大豆饮食和缺碘饮食在N-双(2-羟丙基)亚硝胺[DHPN]引发的大鼠甲状腺肿瘤发生起始后期的调节作用。用含面筋替代酪蛋白的AIN-93G作为基础饮食,以避免可能的碘污染。在实验1中,对雌雄F-344大鼠皮下注射剂量为2800 mg/kg体重的DHPN,然后喂食含0%、0.8%、4%或20%脱脂大豆的饲料12周,用大豆粉按比例替代面筋。尽管任何组均未发现甲状腺增殖性病变,但20%大豆处理组的甲状腺绝对重量显著升高(p<0.01)。在实验2中,在类似皮下注射DHPN后,大鼠在碘正常或缺乏条件下喂食基础饲料或含20%大豆的饲料12周。在碘缺乏而非正常条件下,雌雄大鼠喂食大豆均显著促进了甲状腺滤泡腺瘤(p<0.01)和腺癌(p<0.05)的发生,这与甲状腺素降低和促甲状腺激素升高一致。因此,过量大豆与碘缺乏共同作用可协同促进DHPN引发的大鼠甲状腺肿瘤发生,其机制似乎主要涉及对血清激素水平的影响。

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