Your browser doesn't support javascript.
loading
The Dimethylnitrosamine Induced Liver Fibrosis Model in the Rat.
Chooi, Kum Fai; Kuppan Rajendran, Dinesh Babu; Phang, Siew Siang Gary; Toh, Han Hui Alden.
Afiliación
  • Chooi KF; Technology Development, School of Applied Science, Temasek Polytechnic; chooikf@tp.edu.sg.
  • Kuppan Rajendran DB; Technology Development, School of Applied Science, Temasek Polytechnic.
  • Phang SS; Technology Development, School of Applied Science, Temasek Polytechnic.
  • Toh HH; Technology Development, School of Applied Science, Temasek Polytechnic.
J Vis Exp ; (112)2016 06 17.
Article en En | MEDLINE | ID: mdl-27340889
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Vis Exp Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Vis Exp Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos