通过AOM及AOM联合DSS建立C57BL/6J小鼠结肠癌诱导模型的对比研究(1)
【摘要】 目的 探討使用氧化偶氮甲烷(AOM)及AOM联合葡聚糖硫酸钠(DSS)中不同药物剂量、给药周期及暴露时间对C57BL/6J小鼠建立结肠癌诱导模型效果的影响。方法 分别予低、中、高浓度AOM(10、15、20 mg/kg，每周1次，共4周，每组24只，AOM对照组24只)或AOM(10 mg/kg)联合DSS(一、二、三循环，小鼠数量分别为50、41、29只，DSS对照组40只)干预，对给药后不同时间点处死的小鼠结直肠进行大体与组织病理学评估。结果 单独使用AOM可使小鼠结肠产生异常隐窝灶(ACF)，随着AOM药物浓度和(或)暴露时间增加，ACF数量显著增加(P均<005)。AOM联合DSS可使小鼠结肠形成腺瘤伴高级别上皮内瘤变，相比DSS一循环，DSS二、三循环可显著增加肿瘤发生率、平均成瘤数量、荷瘤小鼠平均成瘤数量及肿瘤体积(P均<005或0008)。结论 C57BL/6J小鼠结直肠ACF随AOM给药浓度及暴露天数增加而增加，AOM联合DSS可加快结直肠癌模型的发生，增加DSS循环可增加成瘤效率。
【关键词】 氧化偶氮甲烷；葡聚糖硫酸钠；结肠癌；动物模型
, 百拇医药
Comparative analysis between application of AOM and AOM/DSS to establish C57BL/6J mouse models with colonic carcinogenesis Zeng Yiwen， Li Jieyao， Tian Kuangyi， Yu Tao， Xu Jihao， Chen Qikui Department of Gastroenterology， Sun Yatsen Memorial Hospital， Sun Yatsen University， Guangzhou 510120， China
Corresponding author，Tian Kuangyi， Email： sttupac@yahoocom
【Abstract】 Objective To evaluate the effect of drug dose， cycle of drug administration and exposure time between azoxymethane (AOM) and AOM combined with dextran sodium sulfate(DSS) in the establishment of C57BL/6J mouse models with colonic carcinogenesis Methods Mice were treated with subcutaneous administration of 10， 15 or 20 mg/kg AOM once a week for 4 weeks (n=24 for each dose group and control group)， or with 10 mg/kg AOM followed by one， two， or three cycles of 2% DSS administration (n=50， 41 and 29 for each cycle group， and n=24 for control group) The colon tissues were collected at different time points after drug administration for gross and histopathological examinations Results Single use of AOM could yield aberrant crypt foci (ACF) The quantity of ACF was significantly increased along with the increasing AOM concentration and/or exposure time (all P<005) Adenomas with highgrade intraepithelial neoplasia were induced in mice treated with AOM in combination with DSS Two or three cycles of DSS could significantly enhance the incidence of tumor， average quantity of tumor， average quantity of tumor in tumorbearing mouse and average tumor volume compared with one cycle of DSS after AOM injection(all P<005 or 0008) Conclusions The quantity of colonic ACF is increased over the increasing AOM concentration and exposure time in C57BL/6J mice Administration of AOM combined with DSS can accelerate the colonic carcinogenesis Increasing the DSS cycle can enhance the efficiency of colonic carcinogenesis
【Key words】 Azoxymethane； Dextran sulfate sodium； Colonic carcinoma； Animal model, 百拇医药(曾一文 黎洁瑶 田旷怡 于涛 许稷豪 陈其奎)
【关键词】 氧化偶氮甲烷；葡聚糖硫酸钠；结肠癌；动物模型
, 百拇医药
Comparative analysis between application of AOM and AOM/DSS to establish C57BL/6J mouse models with colonic carcinogenesis Zeng Yiwen， Li Jieyao， Tian Kuangyi， Yu Tao， Xu Jihao， Chen Qikui Department of Gastroenterology， Sun Yatsen Memorial Hospital， Sun Yatsen University， Guangzhou 510120， China
Corresponding author，Tian Kuangyi， Email： sttupac@yahoocom
【Abstract】 Objective To evaluate the effect of drug dose， cycle of drug administration and exposure time between azoxymethane (AOM) and AOM combined with dextran sodium sulfate(DSS) in the establishment of C57BL/6J mouse models with colonic carcinogenesis Methods Mice were treated with subcutaneous administration of 10， 15 or 20 mg/kg AOM once a week for 4 weeks (n=24 for each dose group and control group)， or with 10 mg/kg AOM followed by one， two， or three cycles of 2% DSS administration (n=50， 41 and 29 for each cycle group， and n=24 for control group) The colon tissues were collected at different time points after drug administration for gross and histopathological examinations Results Single use of AOM could yield aberrant crypt foci (ACF) The quantity of ACF was significantly increased along with the increasing AOM concentration and/or exposure time (all P<005) Adenomas with highgrade intraepithelial neoplasia were induced in mice treated with AOM in combination with DSS Two or three cycles of DSS could significantly enhance the incidence of tumor， average quantity of tumor， average quantity of tumor in tumorbearing mouse and average tumor volume compared with one cycle of DSS after AOM injection(all P<005 or 0008) Conclusions The quantity of colonic ACF is increased over the increasing AOM concentration and exposure time in C57BL/6J mice Administration of AOM combined with DSS can accelerate the colonic carcinogenesis Increasing the DSS cycle can enhance the efficiency of colonic carcinogenesis
【Key words】 Azoxymethane； Dextran sulfate sodium； Colonic carcinoma； Animal model, 百拇医药(曾一文 黎洁瑶 田旷怡 于涛 许稷豪 陈其奎)
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