The effect of rat strain, diet composition and feeding period on the development of a nutritional model of non-alcoholic fatty liver disease in rats
Language English Country Czech Republic Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
21114362
DOI
10.33549/physiolres.932022
PII: 932022
Knihovny.cz E-resources
- MeSH
- Diet adverse effects MeSH
- Dietary Fats adverse effects MeSH
- Glutathione blood MeSH
- Ion Channels biosynthesis MeSH
- Liver chemistry MeSH
- Rats MeSH
- Malondialdehyde metabolism MeSH
- Mitochondrial Proteins biosynthesis MeSH
- Disease Models, Animal MeSH
- Non-alcoholic Fatty Liver Disease MeSH
- Rats, Sprague-Dawley MeSH
- Rats, Wistar MeSH
- Triglycerides blood MeSH
- Uncoupling Protein 2 MeSH
- Fatty Liver etiology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Dietary Fats MeSH
- Glutathione MeSH
- Ion Channels MeSH
- Malondialdehyde MeSH
- Mitochondrial Proteins MeSH
- Triglycerides MeSH
- Ucp2 protein, rat MeSH Browser
- Uncoupling Protein 2 MeSH
Non-alcoholic fatty liver disease (NAFLD) is an important cause of liver-related morbidity and mortality. The aim of this work was to establish and characterize a nutritional model of NAFLD in rats. Wistar or Sprague-Dawley male rats were fed ad libitum a standard diet (ST-1, 10 % kcal fat), a medium-fat gelled diet (MFGD, 35 % kcal fat) and a high-fat gelled diet (HFGD, 71 % kcal fat) for 3 or 6 weeks. We examined the serum biochemistry, the hepatic malondialdehyde, reduced glutathione (GSH) and cytokine concentration, the respiration of liver mitochondria, the expression of uncoupling protein-2 (UCP-2) mRNA in the liver and histopathological samples. Feeding with MFGD and HFGD in Wistar rats or HFGD in Sprague-Dawley rats induced small-droplet or mixed steatosis without focal inflammation or necrosis. Compared to the standard diet, there were no significant differences in serum biochemical parameters, except lower concentrations of triacylglycerols in HFGD and MFGD groups. Liver GSH was decreased in rats fed HFGD for 3 weeks in comparison with ST-1. Higher hepatic malondialdehyde was found in both strains of rats fed HFGD for 6 weeks and in Sprague-Dawley groups using MFGD or HFGD for 3 weeks vs. the standard diet. Expression of UCP-2 mRNA was increased in Wistar rats fed MFGD and HFGD for 6 weeks and in Sprague-Dawley rats using HFGD for 6 weeks compared to ST-1. The present study showed that male Wistar and Sprague-Dawley rats fed by HFGD developed comparable simple steatosis without signs of progression to non-alcoholic steatohepatitis under our experimental conditions.
References provided by Crossref.org
Experimental models of non-alcoholic fatty liver disease in rats