3,5 Diiodo-l-Thyronine (T₂) Promotes the Browning of White Adipose Tissue in High-Fat Diet-Induced Overweight Male Rats Housed at Thermoneutrality

Cells. 2019 Mar 18;8(3):256. doi: 10.3390/cells8030256.

Abstract

The conversion of white adipose cells into beige adipose cells is known as browning, a process affecting energy metabolism. It has been shown that 3,5 diiodo-l-thyronine (T₂), an endogenous metabolite of thyroid hormones, stimulates energy expenditure and a reduction in fat mass. In light of the above, the purpose of this study was to test whether in an animal model of fat accumulation, T₂ has the potential to activate a browning process and to explore the underlying mechanism. Three groups of rats were used: (i) receiving a standard diet for 14 weeks; (ii) receiving a high-fat diet (HFD) for 14 weeks; and (iii) receiving a high fat diet for 10 weeks and being subsequently treated for four weeks with an HFD together with the administration of T₂. We showed that T₂ was able to induce a browning in the white adipose tissue of T₂-treated rats. We also showed that some miRNA (miR133a and miR196a) and MAP kinase 6 were involved in this process. These results indicate that, among others, the browning may be another cellular/molecular mechanism by which T₂ exerts its beneficial effects of contrast to overweight and of reduction of fat mass in rats subjected to HFD.

Keywords: 3,5-diiodo-l-thyronine; browning; energy metabolism; microRNA; obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylate Kinase / metabolism
  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, White / drug effects
  • Adipose Tissue, White / metabolism*
  • Adiposity / drug effects
  • Animals
  • Diet, High-Fat*
  • Diiodothyronines / administration & dosage
  • Diiodothyronines / pharmacology*
  • Down-Regulation / drug effects
  • Fibronectins / blood
  • Housing, Animal*
  • Insulin / metabolism
  • Male
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Overweight / pathology*
  • Phosphorylation / drug effects
  • Rats, Wistar
  • Temperature*
  • Transcription Factors / metabolism
  • Uncoupling Protein 1 / metabolism
  • Up-Regulation / drug effects
  • Weight Gain / drug effects

Substances

  • Diiodothyronines
  • FNDC5 protein, rat
  • Fibronectins
  • Insulin
  • MIRN133 microRNA, rat
  • MicroRNAs
  • PRDM16 protein, rat
  • Transcription Factors
  • Uncoupling Protein 1
  • 3',5'-diiodothyronine
  • Adenylate Kinase