Development of a new diet-induced obesity (DIO) model using Wistar lean rats

Exp Anim. 2018 May 10;67(2):155-161. doi: 10.1538/expanim.17-0079. Epub 2017 Nov 17.

Abstract

Obesity is an increasingly severe socioeconomic health issue worldwide. Rodents with diet-induced obesity (DIO) are widely used as models of obesity. The main aim of this study was to establish a DIO model using Wistar lean (+/+ or +/-) rats by feeding a high-fat diet (45 kcal% fat) to dams during the latter term of gestation and the lactation period. A second aim was to examine the effect of post-weaning nutrition independently of maternal nutrition. Some pups (group D) were fed the same high-fat diet after weaning, while others (group C) were fed a chow diet after weaning. In the control groups, the dams were fed only the chow diet and the pups were fed either the chow diet (group A) or high-fat diet (group B) after weaning. Between 16-21 weeks of age, group D showed the heaviest body weight and visceral adipose tissue weight among groups, in addition to glucose intolerance and high concentrations of glucose and cholesterol in plasma. Group B showed mild obesity with dysfunctions in glucose and lipid metabolism. Interestingly, group C showed mild obesity and impaired glucose tolerance, similar to the phenotype of group B. In summary, the high-fat diet challenge of dams during gestation and lactation caused an increase in adipose tissue weight and abnormalities of glucose and lipid metabolism in their adult offspring. Our results suggest the importance of both maternal and post-weaning nutrition for DIO production and provide useful DIO models.

Keywords: Wistar lean rat; diet-induced obesity (DIO) model; high-fat diet; maternal nutrition; post-weaning nutrition.

MeSH terms

  • Animals
  • Blood Glucose
  • Body Weight
  • Cholesterol / blood
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal*
  • Female
  • Glucose Intolerance
  • Intra-Abdominal Fat / pathology
  • Lipid Metabolism
  • Male
  • Maternal Nutritional Physiological Phenomena
  • Obesity* / etiology
  • Obesity* / metabolism
  • Obesity* / pathology
  • Obesity* / physiopathology
  • Organ Size
  • Pregnancy
  • Rats, Wistar
  • Thinness*

Substances

  • Blood Glucose
  • Cholesterol