Altered food consumption in mice lacking lysophosphatidic acid receptor-1

J Physiol Biochem. 2009 Dec;65(4):345-50. doi: 10.1007/BF03185929.

Abstract

The release of lysophosphatidic acid (LPA) by adipocytes has previously been proposed to play a role in obesity and associated pathologies such as insulin resistance and diabetes. In the present work, the sensitivity to diet-induced obesity was studied in mice lacking one of the LPA receptor subtype (LPA1R). Conversely to what was observed in wild type (WT) mice, LPA1R-KO-mice fed a high fat diet (HFD) showed no significant increase in body weight or fat mass when compared to low fat diet (LFD). In addition, in contrast to what was observed in WT mice, LPA1R-KO mice did not exhibit over-consumption of food associated with HFD. Surprisingly, when fed a LFD, LPA1R-KO mice exhibited significant higher plasma leptin concentration and higher level of adipocyte leptin mRNA than WT mice. In conclusion, LPA1R-KO mice were found to be resistant to diet-induced obesity consecutive to a resistance to fat-induced over-consumption of food that may result at least in part from alterations in leptin expression and production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipose Tissue / metabolism
  • Animal Feed
  • Animals
  • Behavior, Animal*
  • Body Weight
  • Dietary Fats
  • Feeding Behavior*
  • Food
  • Gene Expression Regulation
  • Leptin / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Lysophosphatidic Acid / metabolism*

Substances

  • Dietary Fats
  • Leptin
  • Receptors, Lysophosphatidic Acid