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The Murine Choline-Deficient, Ethionine-Supplemented (CDE) Diet Model of Chronic Liver Injury.
Gogoi-Tiwari, Jully; Köhn-Gaone, Julia; Giles, Corey; Schmidt-Arras, Dirk; Gratte, Francis D; Elsegood, Caryn L; McCaughan, Geoffrey W; Ramm, Grant A; Olynyk, John K; Tirnitz-Parker, Janina E E.
Afiliación
  • Gogoi-Tiwari J; School of Biomedical Sciences & Curtin Health Innovation Research Institute, Curtin University.
  • Köhn-Gaone J; School of Biomedical Sciences & Curtin Health Innovation Research Institute, Curtin University.
  • Giles C; School of Public Health & Curtin Health Innovation Research Institute, Curtin University.
  • Schmidt-Arras D; Institute of Biochemistry, Christian-Albrechts-University.
  • Gratte FD; School of Biomedical Sciences & Curtin Health Innovation Research Institute, Curtin University; School of Veterinary and Life Sciences, Murdoch University.
  • Elsegood CL; School of Biomedical Sciences & Curtin Health Innovation Research Institute, Curtin University.
  • McCaughan GW; Centenary Institute of Cancer Medicine and Cell Biology, The University of Sydney; Royal Prince Alfred Hospital; A.W. Morrow Gastroenterology and Liver Centre.
  • Ramm GA; QIMR Berghofer Medical Research Institute; Faculty of Medicine and Biomedical Sciences, The University of Queensland.
  • Olynyk JK; Fiona Stanley and Fremantle Hospitals; School of Medical and Health Sciences, Edith Cowan University.
  • Tirnitz-Parker JEE; School of Biomedical Sciences & Curtin Health Innovation Research Institute, Curtin University; School of Medicine and Pharmacology, University of Western Australia; N.Tirnitz-Parker@curtin.edu.au.
J Vis Exp ; (128)2017 10 21.
Article en En | MEDLINE | ID: mdl-29155718
Chronic liver diseases, such as viral hepatitis, alcoholic liver disease, or non-alcoholic fatty liver disease, are characterized by continual inflammation, progressive destruction and regeneration of the hepatic parenchyma, liver progenitor cell proliferation, and fibrosis. The end-stage of every chronic liver disease is cirrhosis, a major risk factor for the development of hepatocellular carcinoma. To study processes regulating disease initiation, establishment, and progression, several animal models are used in laboratories. Here we describe a six-week time course of the choline-deficient and ethionine-supplemented (CDE) mouse model, which involves feeding six-week old male C57BL/6J mice with choline-deficient chow and 0.15% DL-ethionine-supplemented drinking water. Monitoring of animal health and a typical body weight loss curve are explained. The protocol demonstrates the gross examination of a CDE-treated liver and blood collection by cardiac puncture for subsequent serum analyses. Next, the liver perfusion technique and collection of different hepatic lobes for standard evaluations are shown, including liver histology assessments by hematoxylin and eosin or Sirius Red stainings, immunofluorescent detection of hepatic cell populations as well as transcriptome profiling of the liver microenvironment. This mouse model is suitable for studying inflammatory, fibrogenic, and liver progenitor cell dynamics induced through chronic liver disease and can be used to test potential therapeutic agents that may modulate these processes.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Deficiencia de Colina / Modelos Animales de Enfermedad / Etionina / Lesión Pulmonar Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Vis Exp Año: 2017 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Deficiencia de Colina / Modelos Animales de Enfermedad / Etionina / Lesión Pulmonar Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Vis Exp Año: 2017 Tipo del documento: Article