Advanced-age C57BL/6JRj mice do not develop obesity upon western-type diet exposure

Adipocyte. 2019 Dec;8(1):105-113. doi: 10.1080/21623945.2019.1590893. Epub 2019 Mar 26.

Abstract

Obesity has become a global health-threat for every age group. It is well known that young mice (10-12 weeks of age) fed a western-type diet (WD) become obese and develop higher cholesterol levels and liver steatosis whereas insulin sensitivity is reduced. Less is known, however, about the effect of a WD on advanced-age mice. Therefore, 10 week-old (young) and 22 month-old (advanced-age), male C57BL/6JRj mice were kept on either a WD or a control diet (SFD) for 15 weeks. In contrast to young mice, advanced-age mice on WD did not show a higher body weight or adipose tissue (AT)-masses, suggesting a protection against diet-induced obesity. Furthermore, plasma adiponectin and leptin levels were not affected upon WD-feeding. A WD, however, did induce more hepatic lipid accumulation as well as increased hepatic expression of the macrophage marker F4/80, in advanced-age mice. There were no significant differences in mRNA levels of uncoupling protein-1 or F4/80 in brown AT (BAT) or of several intestinal integrity markers in colon suggesting that the protection against obesity is not due to excessive BAT or to impaired intestinal absorption of fat. Thus, advanced-age mice, in contrast to their younger counterparts, appeared to be protected against diet-induced obesity.

Keywords: Aging; C57BL/6J mice; obesity; western-type diet.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Adipose Tissue, Brown / metabolism
  • Age Factors*
  • Animals
  • Diet, Western / adverse effects*
  • Fatty Liver
  • Glucose / metabolism
  • Insulin Resistance / physiology
  • Leptin / metabolism
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / metabolism*
  • Uncoupling Protein 1 / metabolism

Substances

  • Leptin
  • Uncoupling Protein 1
  • Glucose

Grants and funding

The Center for Molecular and Vascular Biology was supported by the ‘Programmafinanciering KU Leuven’ (PF/10/014); Onderzoeksraad, KU Leuven [PF/10/014].