首页|AOM/DSS诱导建立结肠炎-癌转化大鼠模型的组织学评价及肠道菌群分析

AOM/DSS诱导建立结肠炎-癌转化大鼠模型的组织学评价及肠道菌群分析

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目的 本研究旨在建立一种表征炎症性肠病炎-癌转化的大鼠模型,并探讨其肠道菌群特征。方法 将成年雄性Wistar大鼠随机分为空白组及葡聚糖硫酸钠(dextran sulfate sodium,DSS)不同干预周期的模型组(M1、M2、M3组)。模型组大鼠均采用单次腹腔注射氧化偶氮甲烷(azoxymethane,AOM)联合自由饮用3个周期DSS的方法诱导结肠炎-癌转化,期间记录疾病活动指数(disease active index,DAI)评分,于DSS第1、2、3周期结束时分别处死M1、M2、M3组大鼠,留取脾、结肠组织及结肠内容物。采用苏木素-伊红(HE)染色、透射电子显微镜观察等方法对各组大鼠结肠组织学损伤及癌变情况进行评估,并采用16S rRNA测序技术分析其肠道菌群的特征性改变。结果 AOM/DSS造模导致了显著的DAI评分上升、结肠缩短及脾指数升高。从M1组到M3组,肠黏膜屏障逐渐破坏,病理评分逐渐升高,依次出现了异常隐窝灶、息肉、低级别上皮内瘤变、高级别上皮内瘤变和黏膜内癌,同时,该病理演变过程表现出与人体炎症性肠病癌变相似的特征。在16S rRNA测序中,采用Wilcoxon和ALDEx2两种差异丰度检验工具筛选得到以拟杆菌门(Bacteroidetes)、单球菌属(Monoglobus)为代表的菌群丰度变化可能参与了结肠炎-癌转化的进展,并观察到差异菌群的功能主要富集到了脂质代谢、碳水化合物代谢等代谢途径。结论 AOM/DSS诱导建立的大鼠模型能较贴切地动态模拟结肠炎-癌转化的病理特点,同时伴随着特定肠道菌群丰度的改变,可能与菌群介导的代谢途径密切相关。
Histological evaluation and analysis of intestinal flora in a rat model of colitis-cancer transformation induced by azoxymethane/dextran sulfate sodium
Objective The aim of this study was to establish a rat model of inflammation-cancer transformation of inflammatory bowel disease(IBD)and to explore the associated characteristics of the intestinal flora.Methods Adult male Wistar rats were divided randomly into control and model groups(M1,M2,M3)with different dextran sulfate sodium(DSS)intervention cycles.Colitis-cancer transformation was induced in all rats in the model group by a single intraperitoneal injection of azoxymethane(AOM)combined with free drinking of DSS in different cycles,and disease activity index(DAI)scores were recorded.Rats in the M1,M2 and M3 groups were killed at the end of the first,second,and third cycles of DSS,respectively,and spleen and colon tissues and colon contents were collected.Histological damage and colon carcinogenesis were evaluated in each group using hematoxylin and eosin staining and transmission electron microscopy.Characteristic changes in the intestinal flora were analyzed by 16S rRNA sequencing.Results AOM/DSS administration significantly increased the DAI score,shortened the colon,and increased the spleen index.The intestinal mucosal barrier was progressively destroyed from groups M1 to M3,and the pathological score was gradually increased.Abnormal crypt foci,polyps,low-and high-grade intraepithelial neoplasia,and mucosal carcinoma appeared in turn,while the pathological process showed similar characteristics to carcinogenesis in human inflammatory bowel disease.Screening using 16S rRNA sequencing with two differential abundance testing tools,Wilcoxon and ALDEx2,indicated that changes in flora abundance represented by Bacteroidetes and Monoglobus may be involved in the progression of colitis-cancer transformation.The functions of the differential flora were mainly enriched in metabolic pathways,such as lipid and carbohydrate metabolism.Conclusions The current rat model induced by AOM/DSS can dynamically simulate the pathological characteristics of colitis-cancer transformation,accompanied by changes in the abundance of specific intestinal flora,which may be closely related to the metabolic pathways mediated by the flora.

colitis associated colorectal cancercolitis-cancer transformationhistopathology16S rRNA sequencingintestinal flora

魏秀楠、孙大娟、梁峻尉、刘佳卉、李公义、迟莉丽

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山东中医药大学第一临床医学院,济南 250014

山东中医药大学附属医院,济南 250014

结肠炎相关性结直肠癌 结肠炎-癌转化 组织病理学 16S rRNA测序 肠道菌群

2024

中国实验动物学报
中国实验动物学会,中国医学科学院医学实验动物研究所

中国实验动物学报

CSTPCD北大核心
影响因子:0.767
ISSN:1005-4847
年,卷(期):2024.32(11)