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胃十二指肠液和膳食脂肪对巴雷特食管及食管肿瘤发生发展的影响:大鼠实验模型

Effect of gastroduodenal juice and dietary fat on the development of Barrett's esophagus and esophageal neoplasia: an experimental rat model.

作者信息

Clark G W, Smyrk T C, Mirvish S S, Anselmino M, Yamashita Y, Hinder R A, DeMeester T R, Birt D F

机构信息

Department of Surgery, University of Southern California School of Medicine, Los Angeles 90033-4612.

出版信息

Ann Surg Oncol. 1994 May;1(3):252-61. doi: 10.1007/BF02303531.

Abstract

BACKGROUND

Reflux of duodenal content into the lower esophagus of rats enhances the formation of nitrosamine-induced esophageal cancer and results in the induction of adenocarcinoma. We investigated the extent of the mucosal injury that was produced when the lower esophagus of rats was exposed to the reflux of gastroduodenal juice in the presence or absence of a carcinogen and tested the hypothesis that induction of esophageal cancer in this model would be influenced by the intake of dietary fat.

METHODS

Esophagoduodenostomy with gastric preservation was performed in 165 Sprague-Dawley rats in order to expose the lower esophagus to the reflux of gastroduodenal juice. Postoperatively selected groups of rats were treated with the carcinogen methyl-n-amylnitrosamine (MNAN). Subsequently, rats were fed diets of differing fat and calorie content for 20 weeks until they were put to death.

RESULTS

Refluxed gastroduodenal juice, in the absence of MNAN, induced esophageal inflammatory changes (diffuse papillomatosis and hyperkeratosis) in 38 of 39 rats (97%), specialized columnar metaplasia (Barrett's esophagus) in four of 39 (10%), dysplasia in three of 39 (8%), and squamous cell carcinoma in one of 39 (3%). Diet did not influence the incidence of neoplasia in the absence of MNAN treatment. In rats treated with MNAN, refluxed gastroduodenal juice induced inflammation in 110 of 111 rats (99%), columnar metaplasia in 14 of 111 (13%), and cancer in 63 of 111 (57%). Fifty-eight percent of esophageal tumors were squamous cell carcinoma and 42% were adenocarcinoma. The highest incidence of tumors was observed in rats fed the semipurified high-fat diet (24 of 29; 83%) compared with rats fed the semipurified control diet (13 of 29; 45%), semipurified, calorie-restricted diet (15 of 27; 55%), and chow diet (11 of 26; 42%), p < 0.05.

CONCLUSIONS

Reflux of gastroduodenal content into the lower esophagus of rats can induce both Barrett's metaplasia and neoplasia. Addition of a carcinogen increases the tumor yield and results in a proportion of the lesions being adenocarcinoma. This carcinogenic process is promoted by a diet with a high fat content.

摘要

背景

十二指肠内容物反流至大鼠食管下段会增强亚硝胺诱导的食管癌形成,并导致腺癌的发生。我们研究了在存在或不存在致癌物的情况下,大鼠食管下段暴露于胃十二指肠液反流时所产生的黏膜损伤程度,并检验了该模型中食管癌的诱导会受到膳食脂肪摄入影响这一假设。

方法

对165只Sprague-Dawley大鼠进行保留胃的食管十二指肠吻合术,以使食管下段暴露于胃十二指肠液反流。术后,选择的大鼠组用致癌物甲基-n-戊基亚硝胺(MNAN)进行处理。随后,给大鼠喂食不同脂肪和热量含量的饮食20周,直至将它们处死。

结果

在不存在MNAN的情况下,反流的胃十二指肠液在39只大鼠中的38只(97%)诱导了食管炎性改变(弥漫性乳头瘤病和角化过度),39只中的4只(10%)出现了特殊的柱状上皮化生(巴雷特食管),其中3只(8%)出现发育异常,1只(3%)出现鳞状细胞癌。在不存在MNAN处理的情况下,饮食并未影响肿瘤形成的发生率。在用MNAN处理的大鼠中,反流的胃十二指肠液在111只大鼠中的110只(99%)诱导了炎症,111只中的14只(13%)出现柱状上皮化生,111只中的63只(57%)出现癌症。58%的食管肿瘤为鳞状细胞癌,42%为腺癌。与喂食半纯化对照饮食(29只中的13只;45%)、半纯化热量限制饮食(27只中的15只;55%)和普通饮食(26只中的11只;42%)的大鼠相比,喂食半纯化高脂肪饮食的大鼠肿瘤发生率最高(29只中的24只;83%),p<0.05。

结论

胃十二指肠内容物反流至大鼠食管下段可诱导巴雷特化生和肿瘤形成。添加致癌物会增加肿瘤发生率,并导致一定比例的病变为腺癌。高脂肪饮食会促进这一致癌过程。

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