Tomato Juice Supplementation Influences the Gene Expression Related to Steatosis in Rats

Nutrients. 2018 Sep 2;10(9):1215. doi: 10.3390/nu10091215.

Abstract

The objective of this work was to identify the effect of tomato juice on the expression of genes and levels of metabolites related to steatosis in rats. Male Sprague Dawley rats (8 weeks-old) were grouped (6 rats/group) in four experimental groups: NA (normal diet and water), NL (normal diet and tomato juice), HA (high-fat diet and water), and HL (high-fat diet and tomato juice). After an intervention period of 5 weeks, rats were sacrificed and biochemical parameters, biomarkers of oxidative stress, liver metabolites, and gene expression were determined. Although the H diet provoked dislipemia related to steatosis, no changes in isoprostanes or liver malondialdehyde (MDA) were observed. Changes in the gene expression of the HA group were produced by the high consumption of fat, whereas the consumption of tomato juice had different effects, depending on the diet. In the NL group, the genes involved in β-oxidation were upregulated, and in groups NL and HL upregulation of CD36 and downregulation of APOB and LPL were observed. In addition, in the HL group the accumulation of lycopene upregulated the genes FXR and HNF4A, which have been suggested as preventive factors in relation to steatosis. Regarding the metabolomics study, intake of tomato juice stimulated the biosynthesis of glutathione and amino acids of the transulfurization pathway, increasing the levels of metabolites related to the antioxidant response.

Keywords: gene expression; lycopene; non-alcoholic fatty liver disease (NAFLD); oxidative biomarkers; quantitative metabolomics.

MeSH terms

  • Amino Acids / biosynthesis
  • Animals
  • Apolipoproteins B / metabolism
  • Biomarkers / metabolism
  • CD36 Antigens / metabolism
  • Dietary Supplements*
  • Down-Regulation
  • Fatty Liver / genetics*
  • Fruit and Vegetable Juices*
  • Gene Expression / physiology*
  • Glutathione / biosynthesis
  • Hepatocyte Nuclear Factor 4 / metabolism
  • Lipoprotein Lipase / metabolism
  • Liver / metabolism
  • Lycopene / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Oxidative Stress / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Solanum lycopersicum*
  • Up-Regulation

Substances

  • Amino Acids
  • Apolipoproteins B
  • Biomarkers
  • CD36 Antigens
  • Hepatocyte Nuclear Factor 4
  • Hnf4a protein, rat
  • Malondialdehyde
  • Lipoprotein Lipase
  • Glutathione
  • Lycopene