Cooke T, Kirkham N, Stainthorp D H, Inman C, Goeting N, Taylor I
Gut. 1984 Jul;25(7):748-55. doi: 10.1136/gut.25.7.748.
Colonic tumours were induced in Wistar rats using 12 consecutive subcutaneous injections of azoxymethane at a dose of 10 mg/kg/week. Pairs of rats were killed at five weekly intervals after initial injection until 25 weeks. Colonic mucosa was sampled from five standard areas along the length of the colon and examined by both scanning electron microscopy and conventional light microscopy. The crypt cell production rate was measured by stathmokinetic techniques. Scanning electron microscopy showed microadenomas as early as five weeks and consistently after 15 weeks. They were found predominantly in the distal colon and increased in size with time. The lesions showed a progressive increase in the number of crypts per adenoma and increasingly disorganised slit shaped crypt orifices. The presence of epithelial dysplasia in the microadenomas and of invasion of the colonic wall by carcinoma was confirmed histologically, although fewer lesions were identified in tissue sections than by scanning electron microscopy. Crypt cell production rate increased with time, particularly in the distal colon. This increase was significant between five and 25 weeks. The results of these observations suggest that there is an adenoma-carcinoma sequence in this animal model. The value of scanning electron microscopy in identifying and quantifying the mucosal changes during carcinogenesis is emphasised.
采用每周10mg/kg的剂量,对Wistar大鼠连续皮下注射12次偶氮甲烷,诱导其发生结肠肿瘤。从初次注射开始,每隔5周处死一对大鼠,直至25周。从结肠全长的5个标准区域采集结肠黏膜,通过扫描电子显微镜和传统光学显微镜进行检查。采用静止动力学技术测量隐窝细胞生成率。扫描电子显微镜显示,早在5周时就出现了微腺瘤,15周后则持续出现。微腺瘤主要位于结肠远端,且随时间推移体积增大。病变显示每个腺瘤的隐窝数量逐渐增加,裂隙状隐窝开口越来越紊乱。组织学证实微腺瘤中存在上皮发育异常以及癌组织对结肠壁的浸润,不过组织切片中发现的病变数量少于扫描电子显微镜检查的结果。隐窝细胞生成率随时间增加,尤其是在结肠远端。这种增加在5至25周之间具有统计学意义。这些观察结果表明,在该动物模型中存在腺瘤 - 癌序列。强调了扫描电子显微镜在识别和量化致癌过程中黏膜变化方面的价值。