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

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. © 2018 Elsevier Inc.

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Adiponectin, Fructose, Interstitial fibrosis, Perisinusoidal fibrosis, Wistar rats, Animals, Diet, Disease models, animal, Kidney, Liver, Male, Non-alcoholic fatty liver disease, Pancreas, Rats, Rats, wistar, Animal cell, Animal experiment, Animal model, Animal tissue, Article, Carbohydrate intake, Cell count, Cell structure, Cell transformation, Controlled study, Disease model, Fibrosing alveolitis, Food composition, Food intake, Hepatic stellate cell, Histopathology, Kidney injury, Kidney tissue, Nonalcoholic fatty liver, Nonhuman, Pancreas injury, Pancreas islet cell, Pancreas tissue, Priority journal, Rat, Reference value, Standardization, Wistar rat, Adverse event, Animal, Drug effect, Pathophysiology

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