Nonalcoholic Steatohepatitis: A Search for Factual Animal Models

• Published in: BioMed research international Vol. 2015; no. 2015; pp. 1 - 13
• Main Authors: da Silva, Deisy Mara, Augusto, Marlei Josiele, Ramalho, Leandra Naira Zambelli, Sanches, Sheila Cristina L., Ramalho, Fernando S.
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01.01.2015; John Wiley & Sons, Inc; Hindawi Limited
• Subjects: Animals; Collagen; Diabetes; Diet; Disease Models, Animal; Disease Progression; Fatty acids; Free radicals; Humans; Insulin resistance; Lipids; Liver; Liver Cirrhosis - genetics; Liver Cirrhosis - physiopathology; Liver diseases; Metabolism; Mice; Morphology; Non-alcoholic Fatty Liver Disease - genetics; Non-alcoholic Fatty Liver Disease - physiopathology; Oxidative stress; Physiological aspects; Rats; Review; Rodents; Triglycerides
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2015/574832

Nonalcoholic fatty liver disease (NAFLD) is characterized by hepatic steatosis, which occurs in the absence of alcohol abuse. NAFLD can evolve into progressive liver injury and fibrosis in the form of nonalcoholic steatohepatitis (NASH). Several animal models have been developed to attempt to represent the morphological, biochemical, and clinical features of human NASH. The actual review presents a critical analysis of the most commonly used experimental models of NAFLD/NASH development. These models can be classified into genetic, nutritional, and a combination of genetic and nutritional factors. The main genetic models are ob/ob and db/db mutant mice and Zucker rats. The principal nutritional models employ methionine- and choline-deficient, high-fat, high-cholesterol and high-cholate, cafeteria, and high-fructose diets. Currently, associations between high-fructose and various compositions of high-fat diets have been widely studied. Previous studies have encountered significant difficulties in developing animal models capable of reproducing human NASH. Some models produce consistent morphological findings, but the induction method differs significantly compared with the pathophysiology of human NASH. Other models precisely represent the clinical and etiological contexts of this disease but fail to provide accurate histopathological representations mainly in the progression from steatosis to liver fibrosis.