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本文引用的文献

1
Sampling blood from the lateral tail vein of the rat.从大鼠的侧尾静脉采集血液。
J Vis Exp. 2015 May 18(99):e52766. doi: 10.3791/52766.
2
Manual restraint and common compound administration routes in mice and rats.小鼠和大鼠的手动保定及常用复合给药途径。
J Vis Exp. 2012 Sep 26(67):2771. doi: 10.3791/2771.
3
Review of experimental models for inducing hepatic cirrhosis by bile duct ligation and carbon tetrachloride injection.胆管结扎和四氯化碳注射诱导肝硬化实验模型的综述。
Acta Cir Bras. 2012 Aug;27(8):589-94. doi: 10.1590/s0102-86502012000800013.
4
Diagnostic necropsy and selected tissue and sample collection in rats and mice.大鼠和小鼠的诊断性尸检及选定组织和样本采集
J Vis Exp. 2011 Aug 7(54):2966. doi: 10.3791/2966.
5
New insights into the antifibrotic effects of sorafenib on hepatic stellate cells and liver fibrosis.索拉非尼抗肝星状细胞及肝纤维化的抗纤维化作用新认识。
J Hepatol. 2010 Jul;53(1):132-44. doi: 10.1016/j.jhep.2010.02.027. Epub 2010 Apr 13.
6
Antifibrotic effects of CGX, a traditional herbal formula, and its mechanisms in rats.CGX,一种传统草药配方,在大鼠中的抗纤维化作用及其机制。
J Ethnopharmacol. 2010 Feb 3;127(2):534-42. doi: 10.1016/j.jep.2009.10.001. Epub 2009 Oct 13.
7
Global gene expression profiling of dimethylnitrosamine-induced liver fibrosis: from pathological and biochemical data to microarray analysis.二甲基亚硝胺诱导的肝纤维化的全基因组表达谱分析:从病理和生化数据到微阵列分析
Gene Expr. 2006;13(2):107-32. doi: 10.3727/000000006783991872.
8
How can transforming growth factor beta be targeted usefully to combat liver fibrosis?如何有效靶向转化生长因子β来对抗肝纤维化?
Eur J Gastroenterol Hepatol. 2004 Feb;16(2):123-6. doi: 10.1097/00042737-200402000-00001.
9
Revised guides for organ sampling and trimming in rats and mice--part 1.大鼠和小鼠器官采样与修整的修订指南——第1部分。
Exp Toxicol Pathol. 2003 Sep;55(2-3):91-106.
10
Toxic liver injury; the metabolism of dimethylnitrosamine.中毒性肝损伤;二甲基亚硝胺的代谢
Biochem J. 1956 Dec;64(4):676-82. doi: 10.1042/bj0640676.

大鼠二甲基亚硝胺诱导性肝纤维化模型

The Dimethylnitrosamine Induced Liver Fibrosis Model in the Rat.

作者信息

Chooi Kum Fai, Kuppan Rajendran Dinesh Babu, Phang Siew Siang Gary, Toh Han Hui Alden

机构信息

Technology Development, School of Applied Science, Temasek Polytechnic;

Technology Development, School of Applied Science, Temasek Polytechnic.

出版信息

J Vis Exp. 2016 Jun 17(112):54208. doi: 10.3791/54208.

DOI:10.3791/54208
PMID:27340889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4927794/
Abstract

Four to six week old, male Wistar rats were used to produce animal models of liver fibrosis. The process requires four weeks of administration of 10 mg/kg dimethylnitrosamine (DMN), given intraperitoneally for three consecutive days per week. Intraperitoneal injections were performed in the fume hood as DMN is a known hepatoxin and carcinogen. The model has several advantages. Firstly, liver changes can be studied sequentially or at particular stages of interest. Secondly, the stage of liver disease can be monitored by measurement of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) enzymes. Thirdly, the severity of liver damage at different stages can be confirmed by sacrifice of animals at designated time points, followed by histological examination of Masson's Trichome stained liver tissues. After four weeks of DMN dosing, the typical fibrosis score is 5 to 6 on the Ishak scale. The model can be reproduced consistently and has been widely used to assess the efficacy of potential anti-fibrotic agents.

摘要

4至6周龄的雄性Wistar大鼠被用于制作肝纤维化动物模型。该过程需要连续四周每周三天腹腔注射10毫克/千克的二甲基亚硝胺(DMN)。由于DMN是一种已知的肝毒素和致癌物,腹腔注射在通风橱中进行。该模型有几个优点。首先,可以在感兴趣的特定阶段或连续地研究肝脏变化。其次,可以通过测量血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)来监测肝脏疾病的阶段。第三,可以在指定时间点处死动物,随后对Masson三色染色的肝脏组织进行组织学检查,以确认不同阶段肝损伤的严重程度。在给予DMN四周后,Ishak评分系统中典型的纤维化评分为5至6分。该模型可以持续再现,并且已被广泛用于评估潜在抗纤维化药物的疗效。