Effect of Ecdysterone on the Hepatic Transcriptome and Lipid Metabolism in Lean and Obese Zucker Rats

Int J Mol Sci. 2021 May 15;22(10):5241. doi: 10.3390/ijms22105241.

Abstract

Conflicting reports exist with regard to the effect of ecdysterone, the predominating representative of steroid hormones in insects and plants, on hepatic and plasma lipid concentrations in different rodent models of obesity, fatty liver, and diabetes, indicating that the effect is dependent on the rodent model used. Here, the hypothesis was tested for the first time that ecdysterone causes lipid-lowering effects in genetically obese Zucker rats. To test this hypothesis, two groups of male obese Zucker rats (n = 8) were fed a nutrient-adequate diet supplemented without or with 0.5 g ecdysterone per kg diet. To study further if ecdysterone is capable of alleviating the strong lipid-synthetic activity in the liver of obese Zucker rats, the study included also two groups of male lean Zucker rats (n = 8) which also received either the ecdysterone-supplemented or the non-supplemented diet. While hepatic and plasma concentrations of triglycerides and cholesterol were markedly higher in the obese compared to the lean rats (p < 0.05), hepatic and plasma triglyceride and cholesterol concentrations did not differ between rats of the same genotype fed the diets without or with ecdysterone. In conclusion, the present study clearly shows that ecdysterone supplementation does not exhibit lipid-lowering actions in the liver and plasma of lean and obese Zucker rats.

Keywords: 20-hydroxyecdysone; cholesterol; ecdysterone; lipid metabolism; liver; obese Zucker rat; obesity; transcriptome; triglyceride.

MeSH terms

  • Animals
  • Dietary Supplements
  • Ecdysterone / metabolism*
  • Ecdysterone / pharmacology*
  • Fructosamine / blood
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Genotype
  • Lipid Metabolism / drug effects
  • Lipid Metabolism / physiology*
  • Lipids / blood
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Obesity / metabolism*
  • Organ Size / drug effects
  • Rats
  • Rats, Zucker
  • Reproducibility of Results

Substances

  • Lipids
  • Fructosamine
  • Ecdysterone