Table 1.
Dietary animal models of NASH.
| Model name | Characteristics |
|---|---|
| Methionine and choline-deficient diet |
Pros: Histological NASH by 2-4 weeks Cons: Weight loss and absence of insulin resistance |
| Choline-deficient L-amino-defined diet |
Pros: Histological NASH and hepatocarcinogenesis Cons: Weight stability and absence of insulin resistance |
| Cholesterol and cholate |
Pros: Histological NASH by 6-24 weeks, dyslipidaemia, lipoperoxidation and oxidative stress but the major Cons: Absence of insulin resistance, weight loss of 9% and low serum triglycerides |
| High cholesterol diet |
Pros: Insulin resistance, increase in free fatty acids, triglycerides and serum aminotransferase levels Cons: Small weight gain and not pronounced liver histological changes, level of dietary cholesterol not applicable to humans |
| High-fat diet | Pros: Insulin resistance, histological NASH by 16 weeks. Cons: Phenotype is not severe |
| High-fructose -fat and -cholesterol diet |
Pros: Insulin resistance, histological NASH, liver and fat inflammation. Cons: Not progression to liver advanced fibrosis and carcinogenesis |
| The streptozocin high-fat diet model |
Pros: Histological NASH by 20 weeks, progressive liver fibrosis ad HCC. Cons: Beta cells loss function induced by chemical agent and not by insulin resistance et systemic inflammation, transcriptomics profoundly different from humans |
| Diet-induced animal model of NAFLD (DIAMOND) | Pros: Obesity, insulin resistance, dyslipidaemia, liver inflammation by 16 weeks, cirrhosis by 36 weeks and HCC, activation of the unfolded protein response, oxidative stress, apoptosis, fibrogenic process, serum adiponectin reduction and adipose tissue inflammation, concordance in transcriptomic analysis and histological features of HCC similar in mice and human NASH |
| Western-like diet |
Pros: Induce hepatic steatosis, NASH and fibrosis Cons: Diet composition is not comparable to human diet |
| Diet- and chemical-induced murine NASH |
Pros: Induce hepatic steatosis, insulin resistance, NASH and HCC. Same liver transcriptomic dysregulation of human NASH Cons: Small weight gain |
HCC, hepatocellular carcinoma; NASH, non-alcoholic steatohepatitis.