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胆总管内注射无水乙醇致胆道闭锁动物模型的建立
引用本文:葛军涛,李龙,魏延栋,王海斌,乔国梁,张震,刘垚,明安晓.胆总管内注射无水乙醇致胆道闭锁动物模型的建立[J].实验动物与比较医学,2014,22(3):50-52.
作者姓名:葛军涛  李龙  魏延栋  王海斌  乔国梁  张震  刘垚  明安晓
作者单位:首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020;首都儿科研究所, 北京 100020
基金项目:国家自然科学基金面上项目,先天性胆道畸形肝脏损伤及修复机制研究(81170335).
摘    要:目的 应用胆总管内注射无水乙醇建立SD大鼠胆道闭锁模型. 方法 将SD雄性大鼠随机分为实验组和对照组,在实验组中经静脉留置针插入胆总管注入无水乙醇,对照组注入生理盐水.观察SD大鼠的生化及病理结果. 结果 在实验组中SD大鼠根据病理及生化检测分为肝功能持续恶化组和肝功能修复组,肝功能持续恶化组在8周以后生化明显高于对照组及肝功能修复组.常规HE染色及SMA、Masson染色也出现明显变化.结论 胆总管无水乙醇注射诱导胆道闭锁模型是一种可靠的动物模型,此动物模型会帮助人们进一步研究胆道闭锁提供更多的研究手段.

关 键 词:胆道闭锁  肝硬化  无水乙醇  大鼠模型
收稿时间:2014/3/13 0:00:00

Injection of ethanol into the common bile duct to establish a rat model of biliary atresia
GE Jun-tao,LI Long,WEI Yan-dong,WANG Hai-bin,QIAO Guo-liang,ZHANG Zhen,LIU Yao and MING An-xiao.Injection of ethanol into the common bile duct to establish a rat model of biliary atresia[J].Laboratory Animal and Comparative Medicine,2014,22(3):50-52.
Authors:GE Jun-tao  LI Long  WEI Yan-dong  WANG Hai-bin  QIAO Guo-liang  ZHANG Zhen  LIU Yao and MING An-xiao
Institution:Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China;Capital Institute of Pediatrics, Beijing 100021, China
Abstract:Objective To establish a new rat model of biliary atresia by pure ethanol injection into the common bile duct. Methods A catheter was inserted and fixed in the common bile duct in male SD rats. Saline (8 rats) or pure ethanol (16 rats) was injected through the catheter,respectively, and the biochemical and pathological changes in the rats were examined. Results SD rats in the experimental group were divided into a persistent injury and a restoration of liver dysfunction groups according to pathological and biochemical detection. In the persistent injury group, biochemical impairments were significantly higher at 8 weeks after ethanol injection than those in the control group and restoration group. Distinct pathological changes in the liver were observed using HE, SMA, and Masson staining. Conclusions It is a reliable animal model of biliary atresia induced by injection of pure ethanol into the common bile duct in the rat. It will provide a useful tool in future studies of biliary atresia.
Keywords:Biliary atresia  Liver cirrhosis  Pure ethanol  Rat  model
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