Effects of obesity on the relationship of leptin mRNA expression and adipocyte size in anatomically distinct fat depots in mice

Am J Physiol Regul Integr Comp Physiol. 2004 Jul;287(1):R112-9. doi: 10.1152/ajpregu.00028.2004. Epub 2004 Mar 4.

Abstract

In support of leptin's physiological role as humoral signal of fat mass, we have shown that adipocyte volume is a predominant determinant of leptin mRNA levels in anatomically distinct fat depots in lean young mice in the postabsorptive state. In this report, we investigated how obesity may affect the relationship between leptin mRNA levels and adipocyte volume in anatomically distinct fat depots in mice with genetic (Lep(ob)/Lep(ob) and A(y)/+), diet-induced, and aging-related obesity. In all of the obese mice examined, tissue leptin mRNA levels relative to the average adipocyte volume were lower in the perigonadal and/or retroperitoneal than in the inguinal fat depots and were lower than those of the lean young mice in the perigonadal fat depot. A close, positive correlation between leptin mRNA level and adipocyte volume was present from small to hypertrophic adipocytes within each perigonadal and inguinal fat pad in the obese mice, but the slopes of the regression lines relating leptin mRNA level to adipocyte volume were significantly lower in the perigonadal than in the inguinal fat pads of the same mice. These results suggest that obesity per se is associated with a decreased leptin gene expression per unit of fat mass in mice and that the positive correlation between leptin mRNA level and adipocyte volume is an intrinsic property of adipocytes that is not disrupted by adipocyte hypertrophy in obese mice.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipocytes / physiology*
  • Adipocytes / ultrastructure*
  • Adipose Tissue / metabolism*
  • Adipose Tissue / ultrastructure
  • Animals
  • Cell Size / genetics
  • Cell Size / physiology
  • Diet
  • Dietary Fats / pharmacology
  • Leptin / biosynthesis*
  • Leptin / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / genetics
  • Obesity / metabolism*
  • RNA, Messenger / biosynthesis*
  • Receptors, Glucocorticoid / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Dietary Fats
  • Leptin
  • RNA, Messenger
  • Receptors, Glucocorticoid