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Chemoprevention of 12-dimethylhydrazine-induced colonic preneoplastic lesions in Fischer rats by 6-methylsulfinylhexyl isothiocyanate a wasabi derivative

机译:6-甲基亚磺酰基己基异硫氰酸酯(芥末衍生物)化学预防Fischer大鼠12-二甲基肼诱发的结肠癌前病变

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摘要

The preventive effects of dietary exposure to a wasabi derivative 6-methylsulfinylhexyl isothiocyanate (6-MSITC) during the initiation and post-initiation phases on the development of 1,2-dimethylhydrazine (DMH)-induced colonic aberrant crypt foci (ACF), and β-catenin-accumulated crypts (BCAC) were investigated in male F344 rats. To induce ACF and BCAC, rats were given four weekly subcutaneous injections of DMH (40 mg/kg body weight). The rats also received diets containing 200 or 400 ppm 6-MSITC during the initiation or post-initiation phases. The experiment was terminated 12 weeks after the start. DMH exposure produced a substantial number of ACF (323.8±69.7/colon) and BCAC (3.80±1.05/cm2) at the end of the study. Dietary administration of 6-MSITC at a dose of 400 ppm during the initiation phase caused a significant reduction in the total number of ACF (52% reduction, P<0.0001), larger ACF (4 or more crypt ACF) (58% reduction, P<0.001) and BCAC (76% reduction, P<0.00001). The dietary exposure to 6-MSITC significantly reduced the size (crypt multiplicity) of BCAC during both initiation and post-initiation treatment when compared to group 1 treated with DMH alone. Immunohistochemically, 6-MSITC administration lowered the proliferating cell nuclear antigen labeling index in ACF and BCAC. In addition, protein levels of hepatic cytochrome P-450 isozymes at 24 h after 6-MSITC exposure were significantly suppressed (P<0.01). The results indicated that 6-MSITC exerted chemopreventive effects in the present short-term colon carcinogenesis bioassay, through alterations in cell proliferation activity and drug metabolizing enzyme levels.
机译:在启动和启动后阶段,饮食中芥末衍生物6-甲基亚磺酰基己基异硫氰酸酯(6-MSITC)的饮食暴露对1,2-二甲基肼(DMH)诱导的结肠畸形隐窝灶(ACF)发育的预防作用;以及在雄性F344大鼠中研究了β-catenin积累的隐窝(BCAC)。为了诱导ACF和BCAC,对大鼠每周进行四次DMH皮下注射(40 mg / kg体重)。在开始或开始后阶段,大鼠还接受了含有200或400 ppm 6-MSITC的饮食。实验在开始12周后终止。在研究结束时,暴露于DMH会产生大量的ACF(323.8±69.7 / cm)和BCAC(3.80±1.05 / cm 2 )。在起始阶段以400 ppm的剂量饮食施用6-MSITC导致ACF总数显着减少(减少52%,P <0.0001),较大的ACF(减少4个或更多隐窝ACF)(减少58%, P <0.001)和BCAC(降低76%,P <0.00001)。与单独用DMH进行治疗的第1组相比,饮食中6-MSITC的暴露量显着降低了起始和起始后治疗期间BCAC的大小(隐窝多样性)。免疫组织化学分析,6-MSITC给药可降低ACF和BCAC中增殖细胞核抗原标记指数。此外,在6-MSITC暴露后24 h,肝细胞色素P-450同工酶的蛋白质水平被显着抑制(P <0.01)。结果表明6-MSITC通过改变细胞增殖活性和药物代谢酶水平在当前的短期结肠癌发生生物测定中发挥化学预防作用。

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