Enhanced expression of uncoupling protein 2 gene in rat white adipose tissue and skeletal muscle following chronic treatment with thyroid hormone

FEBS Lett. 1997 Dec 1;418(3):323-6. doi: 10.1016/s0014-5793(97)01404-x.

Abstract

Evidence is rapidly emerging which suggests that uncoupling protein 2 (UCP2), by virtue of its ubiquitous expression, may be important for determining basal metabolic rate. To assess the functional modulation of UCP2 gene expression in relation to body weight control, we examined the effects of hyperthyroid state induced by chronic treatment with triiodothyronine (T3) on UCP2 mRNA expression in male rats. Daily subcutaneous injection of T3 (37 pmol/100 g body weight) for 7 days increased UCP2 mRNA expression in brown adipose tissue (BAT), white adipose tissue (WAT) and the soleus muscle 1.6-, 1.6- and 1.7-fold compared to the controls, respectively, and increased UCP1 mRNA expression in BAT 1.2-fold. In contrast, the same treatment with T3 decreased both ob mRNA expression in WAT and plasma leptin level 0.5-fold for each. The present results suggest that T3 may directly increase UCP2 expression independently of leptin action.

MeSH terms

  • Adipose Tissue / metabolism*
  • Animals
  • Gene Expression Regulation / drug effects*
  • Ion Channels
  • Male
  • Membrane Transport Proteins*
  • Mitochondrial Proteins*
  • Muscle, Skeletal / metabolism*
  • Protein Biosynthesis*
  • Proteins / genetics
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Triiodothyronine / administration & dosage*
  • Uncoupling Protein 2

Substances

  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • Proteins
  • RNA, Messenger
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • Triiodothyronine