Effect of Weight-Reduction in Obese Mice Lacking Toll-Like Receptor 5 and C57BL/6 Mice Fed a Low-Fat Diet

Mediators Inflamm. 2015:2015:852126. doi: 10.1155/2015/852126. Epub 2015 Nov 23.

Abstract

Background: This study aims to investigate the effect of feeding low-fat diet (LFD) to diet-induced obesity (DIO) mice lacking TLR5 (TLR5(-/-)), which have a tendency to develop glucose intolerance with increased adiposity, compared to that in C57BL/6 mice.

Results: TLR5(-/-) and C57BL/6 male mice were divided into three subgroups: (1) control, mice were fed a standard AIN-76A (fat: 11.5 kcal%) diet for 12 weeks; (2) DIO, mice were fed a 58 kcal% high-fat diet (HFD) for 12 weeks; and (3) diet, mice were fed a HFD for 8 weeks to induce obesity and then switched to a 10.5 kcal% LFD for 4 weeks. The glucose intolerance in DIO TLR5(-/-) mice was more significant than that in DIO C57BL/6 mice and was not attenuated by a switch to the LFD. Weight-reduction with LFD had significantly decreased the epididymal fat mass in C57BL/6 mice but not in TLR5(-/-) mice. In addition, the LFD-fed TLR5(-/-) mice showed significantly higher expression of ghrelin in the serum and resistin in the epididymal fat than that in C57BL/6 mice.

Conclusions: This study demonstrated that TLR5 gene knockout impairs some effects of weight-reduction in DIO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity
  • Animals
  • Cytokines / blood
  • Diet, Fat-Restricted*
  • Diet, High-Fat / adverse effects
  • Ghrelin / blood
  • Glucose Intolerance / etiology
  • Glucose Intolerance / immunology
  • Glucose Intolerance / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / diet therapy*
  • Obesity / immunology*
  • Obesity / metabolism
  • Resistin / metabolism
  • Toll-Like Receptor 5 / deficiency*
  • Toll-Like Receptor 5 / genetics
  • Weight Gain
  • Weight Loss

Substances

  • Cytokines
  • Ghrelin
  • Resistin
  • Retn protein, mouse
  • Toll-Like Receptor 5