Differences in mRNA expression of adipocyte-derived factors in response to fasting, refeeding and leptin

Biochim Biophys Acta. 2004 Jul 5;1683(1-3):101-9. doi: 10.1016/j.bbalip.2004.05.001.

Abstract

The present study examines whether and to what extent the profiles of adipose-derived factors are altered in epididymal and subcutaneous adipose tissues of long-term fasted/refed and of fasted rats treated by recombinant leptin. Fasting was characterized by three successive metabolic phases. Minor differences in the time-course and magnitude of response were detected between the two adipose sites. Leptin, adiponectin, resistin, adiponutrin, and insulin-like growth factor-1 (IGF-1) gene expressions differentially decreased according to the fasting duration. mRNA levels reached a minimum in late fasting for these secreted factors, being decreased by 60-90% for adiponectin, resistin, and IGF-1, 95-98% for leptin and by 100% for adiponutrin. Refeeding partially or totally restored their mRNA expression in epididymal adipose. Expression levels of apolipoprotein E (ApoE), angiotensinogen (AGT), adipsin and macrophage migration inhibitory factor (MIF) were either unchanged or slightly affected. In leptin-treated rats, leptin mRNA concentrations were significantly decreased in phase 2 of fasting (by 85%) from levels in control phosphate-buffered saline (PBS)-treated rats in both tissues. Leptin treatment also decreased resistin mRNA levels (by 78% in P2L and 63% in P3L relative to control groups) in subcutaneous adipose. These data suggest that adiponectin, resistin, adiponutrin, and IGF-1 could be involved in overall energy homeostasis during prolonged fasting, as leptin is. The mechanisms that underlie the expressions of these adipose-secreted factors remain to be determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin
  • Adipose Tissue / metabolism*
  • Animals
  • Eating*
  • Epididymis
  • Fasting*
  • Hormones, Ectopic / genetics*
  • Hormones, Ectopic / metabolism
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Intercellular Signaling Peptides and Proteins*
  • Leptin / pharmacology*
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Nitrogen / metabolism
  • Proteins / genetics*
  • Proteins / metabolism
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Resistin
  • Urea / urine

Substances

  • Adiponectin
  • Hormones, Ectopic
  • Intercellular Signaling Peptides and Proteins
  • Leptin
  • Membrane Proteins
  • Proteins
  • RNA, Messenger
  • Resistin
  • Retn protein, rat
  • adiponutrin
  • Insulin-Like Growth Factor I
  • Urea
  • Nitrogen