Fructose threshold for inducing organ damage in a rat model of nonalcoholic fatty liver disease

Nutr Res. 2019 Feb:62:101-112. doi: 10.1016/j.nutres.2018.11.003. Epub 2018 Nov 9.

Abstract

A fructose-enriched diet has been shown to be associated with an increase in fatty infiltration of liver, kidney, and pancreas. Our objective was to determine the concentration threshold at which a fructose-enriched diet induces damage in these organs. We hypothesized that a 20% fructose-enriched diet will induce steatosis or histopathological changes in the kidneys or pancreas. In this study, 40 Wistar male rats were randomly divided into 4 groups of 10, and each group was assigned a diet of equal quantity (15 g/rat) but of varying fructose amount. The first group (control group) was fed a standardized diet. The second and third groups were fed 10% and 20% fructose-enriched diets, respectively, whereas the fourth group was fed a high-fructose diet (30% fructose). At week 16, the 30% fructose group had the highest percentage of fat-enriched cells (10%) and a significant decrease in adiponectin as compared with week 1 (P < .05). Twenty percent of this group developed interstitial fibrosis, but none presented changes in the pancreatic islet structure or fibrosis. The 10% fructose group showed the absence of perisinusoidal and interstitial fibrosis, whereas these were present in the 20% fructose group, but neither group showed significant steatosis (5%) or pancreatic damage. The results suggest that a 20% fructose-enriched diet could be considered as the threshold for inducing kidney and liver damage in the rat. Nutritional interventions to reduce fructose to less than 20% of the total energy intake should be considered to prevent metabolic risks and organ damage.

Keywords: Adiponectin; Fructose; Interstitial fibrosis; Perisinusoidal fibrosis; Wistar rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diet / adverse effects*
  • Disease Models, Animal
  • Fructose / adverse effects*
  • Kidney / drug effects*
  • Kidney / physiopathology
  • Liver / drug effects*
  • Liver / physiopathology
  • Male
  • Non-alcoholic Fatty Liver Disease / physiopathology*
  • Pancreas / drug effects*
  • Pancreas / physiopathology
  • Rats
  • Rats, Wistar

Substances

  • Fructose