Liver fat accumulation may be dissociated from adiposity gain in ovariectomized rats

Climacteric. 2012 Dec;15(6):594-601. doi: 10.3109/13697137.2011.637650. Epub 2012 Jan 23.

Abstract

Objective: The purpose of the present study was to establish a model of rats prone and resistant to intra-abdominal fat accumulation in response to ovariectomy (Ovx-P and Ovx-R) and to determine its relationship with molecular biomarkers.

Design: Two experiments were conducted in which female rats were either sham-operated (Sham) or ovariectomized (Ovx). In the first experiment, ovariectomized rats were stratified into three tertiles based on intra-abdominal adipose tissue mass. To strengthen the Ovx-P/Ovx-R model, we conducted a second experiment in which the numbers of rats in each group were extended and in which different molecular markers were measured. At the end of a 6-8-week period, ovariectomized rats that displayed the lower abdominal fat accumulation (lower tertile) were labelled as Ovx-R and those in the upper tertile as Ovx-P.

Results: Ovx-R rats displayed similar abdominal fat gain to Sham rats whereas Ovx-P rats depicted abdominal fat mass twice as high as that of Sham and Ovx-R rats. Despite the difference in abdominal adiposity, liver fat content was ~50% higher (p < 0.01) in both Ovx-R and Ovx-P rats compared to Sham rats. In addition, both Ovx-R and Ovx-P rats depicted higher HOMA-IR scores (p < 0.05) and lower (p < 0.01) hepatic gene expression of leptin receptor-b and -e, microsomal transfer protein (MTP), and diacylglycerol acyltransferase-2 (DGAT-2) compared to Sham rats.

Conclusion: The present findings indicate that estrogen withdrawal-induced hepatic steatosis and associated insulin resistance may be dissociated from abdominal fat accumulation and suggest that a decrease in leptin action through a down-regulation of leptin receptors and a decrease in very low density lipoprotein production through a down-regulation of MTP and DGAT-2 may be factors responsible for this observation in the absence of peripheral fat gain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Fat
  • Adiposity / physiology*
  • Animals
  • Carrier Proteins / genetics
  • Diacylglycerol O-Acyltransferase / genetics
  • Fatty Liver / etiology*
  • Fatty Liver / metabolism
  • Female
  • Gene Expression
  • Insulin Resistance
  • Liver / metabolism
  • Ovariectomy*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Leptin / genetics

Substances

  • Carrier Proteins
  • RNA, Messenger
  • Receptors, Leptin
  • microsomal triglyceride transfer protein
  • DGAT2 protein, human
  • Diacylglycerol O-Acyltransferase