Lipid metabolism in adipose tissue and liver from diet-induced obese rats: a comparison between Wistar and Sprague-Dawley strains

J Physiol Biochem. 2018 Nov;74(4):655-666. doi: 10.1007/s13105-018-0654-9. Epub 2018 Nov 9.

Abstract

Some researchers have proposed important variations in adipose tissue among different strains of rats and mice in response to a high-caloric (hc) diet, but data concerning the mechanisms underlying these differences are scarce. The aim of the present research was to characterize different aspects of triacylglycerol (TG) metabolism and clock genes between Sprague-Dawley and Wistar rats. For this purpose, 16 male Sprague-Dawley and 16 male Wistar rats were divided into four experimental groups (n = 8) and fed either a normal-caloric (nc) diet or a hc diet for 6 weeks. After sacrifice, liver and epididymal, perirenal, mesenteric, and subcutaneous adipose tissue depots were dissected, weighed and immediately frozen. Liver TG content was quantified, RNA extracted for gene expression analysis and fatty acid synthase enzyme activity measured. Two-way ANOVA and Student's t test were used to perform the statistical analyses. Under hc feeding conditions, Wistar rats were more prone to fat accumulation in adipose tissue, especially in the epididymal fat depot, due to their increased lipogenesis and fatty acid uptake. By contrast, both strains of rats showed similarly fatty livers after hc feeding. Peripheral clock machinery seems to be a potential explanatory mechanism for Wistar and Sprague-Dawley strain differences. In conclusion, Wistar strain seems to be the best choice as animal model in dietary-induced obesity studies.

Keywords: High-caloric feeding; Obesity; Rats; Sprague-Dawley; Strain; Wistar.

Publication types

  • Comparative Study

MeSH terms

  • Adiposity
  • Animals
  • CLOCK Proteins / genetics
  • CLOCK Proteins / metabolism
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal*
  • Fatty Acid Synthases / genetics
  • Fatty Acid Synthases / metabolism
  • Gene Expression Regulation, Enzymologic
  • Intra-Abdominal Fat / enzymology
  • Intra-Abdominal Fat / metabolism*
  • Intra-Abdominal Fat / pathology
  • Lipogenesis*
  • Liver / enzymology
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Non-alcoholic Fatty Liver Disease / etiology
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Non-alcoholic Fatty Liver Disease / pathology
  • Obesity / etiology
  • Obesity / metabolism*
  • Obesity / pathology
  • Organ Size
  • Organ Specificity
  • Random Allocation
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Species Specificity
  • Subcutaneous Fat, Abdominal / enzymology
  • Subcutaneous Fat, Abdominal / metabolism*
  • Subcutaneous Fat, Abdominal / pathology
  • Triglycerides / metabolism
  • Weight Gain

Substances

  • Triglycerides
  • CLOCK Proteins
  • Fatty Acid Synthases