The role of receptor-interacting protein 140 in the accumulation of fat in ovariectomised rats

Obes Surg. 2011 Jul;21(7):935-40. doi: 10.1007/s11695-010-0241-9.

Abstract

Background: Receptor-interacting protein 140 (RIP140) is a corepressor for nuclear receptors with an important role in the inhibition of energy expenditure. Postmenopausal women have increased white adipose tissue (WAT), and excessive accumulation of adipose tissue (obesity) implies a health risk. The aim of the present work was to investigate the time course of RIP140 expression in WAT during the development of ovariectomy (OVX)-induced obesity in rats.

Methods: OVX was performed in female Sprague-Dawley (SD) rats 8 weeks old. Body weight and food intake were determined once a week. WAT of sham-operated, OVX and OVX plus 17β-estradiol therapy (OVX/E2) female SD rats was weighed and used to analyse RIP140 and uncoupling protein 1 (UCP-1) expression by Western blot.

Results: Food intake and body weight were significantly increased during the 2-8 weeks after OVX. Even though body weight increased until killing, food intake progressively decreased from 9 to 16 weeks after OVX in rats. Meanwhile, increased WAT mass and decreased RIP140 expression in WAT were observed in OVX rats. In contrast, the expression of UCP-1, a key target gene of RIP140, in WAT of OVX rats was significantly higher than in sham-operated rats. All of these alterations caused by OVX were mostly reversed by the replacement of 17β-estradiol.

Conclusions: The down-regulation of RIP140 in WAT may play a compensatory role in OVX-induced obesity in rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / biosynthesis*
  • Adipose Tissue, White / metabolism*
  • Adiposity / physiology*
  • Animals
  • Appetite Regulation / physiology
  • Blotting, Western
  • Body Weight
  • Down-Regulation
  • Eating
  • Estradiol / administration & dosage
  • Estradiol / metabolism
  • Estrogens / administration & dosage
  • Estrogens / metabolism
  • Female
  • Ion Channels / biosynthesis
  • Menopause / metabolism*
  • Mitochondrial Proteins / biosynthesis
  • Nuclear Proteins / biosynthesis*
  • Nuclear Receptor Interacting Protein 1
  • Obesity / metabolism*
  • Ovariectomy*
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Uncoupling Protein 1

Substances

  • Adaptor Proteins, Signal Transducing
  • Estrogens
  • Ion Channels
  • Mitochondrial Proteins
  • Nuclear Proteins
  • Nuclear Receptor Interacting Protein 1
  • Ucp1 protein, rat
  • Uncoupling Protein 1
  • Estradiol