首页> 外文期刊>Cancer science. >Combined treatment with green tea catechins and sodium nitrite selectively promotes rat forestomach carcinogenesis after initiation with N-methyl-N'- nitro-N-nitrosoguanidine.
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Combined treatment with green tea catechins and sodium nitrite selectively promotes rat forestomach carcinogenesis after initiation with N-methyl-N'- nitro-N-nitrosoguanidine.

机译:N-甲基-N'-硝基-N-亚硝基胍引发的绿茶儿茶素和亚硝酸钠的联合处理选择性促进大鼠前胃癌的发生。

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Combined treatment with several phenolic antioxidants and sodium nitrite (NaNO(2)) has already shown to enhance rat forestomach carcinogenesis. In the present experiment, effects of green tea catechins (GTC) alone or in combination with NaNO(2) on gastric carcinogenesis were investigated in a rat two-stage carcinogenesis model. Groups of eight, 6-week-old F344 male rats were given 0.01%N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) in their drinking water and 5% NaCl in the diet for 10 weeks for glandular stomach initiation and a single intragastric administration of 100 mg/kg/bodyweight of MNNG at week 9 for forestomach initiation. From week 11, they received either drinking water containing 0.2% NaNO(2) and a diet supplemented with 1% GTC in combination, each individual chemical alone or a basal diet until the end of week 42. In the forestomach, incidences and multiplicities of neoplastic lesions were clearly increased by the combined treatment, in spite of GTC alone suppressing the occurrence of papillomas. In a short-term experiment with similar protocol without MNNG pretreatment, a significant increase of 8-hydroxydeoxyguanosine (8-OHdG) levels in forestomach DNA occurred 24 h after the combined treatment, concomitant with erosion and inflammatory cell infiltration. In an in vitro study, electron spin resonance demonstrated hydroxyl radical formation after incubation of epigallocatechin gallate or epicatechin gallate with the NO generator, NOC-7. Thus, GTC alone showed a weak chemopreventive effect on forestomach carcinogenesis, but in the presence of NaNO(2) it exerted a promotive effect which might involve hydroxyl-radical-associated oxidative DNA damage. However, no influence was exerted in the glandular stomach.
机译:与几种酚类抗氧化剂和亚硝酸钠(NaNO(2))的联合治疗已经显示出可以增强大鼠前胃癌的发生。在本实验中,在大鼠的两阶段癌变模型中研究了绿茶儿茶素(GTC)单独或与NaNO(2)联合对胃癌发生的作用。八只6周大的F344雄性大鼠的组在其饮用水中给予0.01%N-甲基-N'-硝基-N-亚硝基胍(MNNG),在饮食中给予5%NaCl,持续10周以进行腺胃启动和在第9周进行一次胃内施用MNNG的剂量为100 mg / kg /体重,以启动前胃病。从第11周开始,他们接受了含0.2%NaNO(2)的饮用水和补充了1%GTC的饮食,单独使用每种化学药品或基础饮食,直到第42周结束。尽管单独使用GTC抑制了乳头状瘤的发生,但联合治疗仍明显增加了肿瘤性病变。在一项未经MNNG预处理的类似方案的短期实验中,联合治疗后24小时,前胃DNA中的8-羟基脱氧鸟苷(8-OHdG)水平显着增加,并伴有糜烂和炎性细胞浸润。在一项体外研究中,电子自旋共振表明将表没食子儿茶素没食子酸酯或表儿茶素没食子酸酯与NO生成器NOC-7孵育后形成了羟基自由基。因此,仅GTC对前胃癌的致癌作用显示出较弱的化学预防作用,但在NaNO(2)的存在下,它发挥了促进作用,可能涉及羟基自由基相关的氧化DNA损伤。但是,对腺胃没有影响。

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