Peroxisome proliferator-activated receptor alpha (PPARalpha) activators, bezafibrate and Wy-14,643, increase uncoupling protein-3 mRNA levels without modifying the mitochondrial membrane potential in primary culture of rat preadipocytes

Arch Biochem Biophys. 2000 Aug 15;380(2):353-9. doi: 10.1006/abbi.2000.1927.

Abstract

Uncoupling proteins (UCPs) are inner mitochondrial membrane transporters which act as pores for H(+) ions, dissipating the electrochemical gradient that develops during mitochondrial respiration at the expense of ATP synthesis. We have studied the effects of two fibrates, bezafibrate and Wy-14,643, on UCP-3 and UCP-2 mRNA levels in primary monolayer cultures of rat adipocytes and undifferentiated preadipocytes. Treatment with both PPARalpha activators for 24 h up-regulated UCP-3 mRNA levels. Thus, bezafibrate treatment resulted in an 8-fold induction in UCP-3 mRNA levels in preadipocytes compared with the 3.5-fold induction observed in adipocytes. Differences in the induction of UCP-3 between these cells correlated well with the higher expression of PPARalpha and RXRalpha mRNA values in preadipocytes compared to adipocytes. Wy-14,643 caused similar effects on UCP-3 mRNA expression. In contrast to UCP-3, UCP-2 mRNA levels were only slightly modified by bezafibrate in adipocytes. The induction in UCP-3 expression was not accompanied by changes in the mitochondrial membrane potential of rat primary preadipocytes after bezafibrate or Wy-14,643 treatment. Since it has been proposed that UCP-3 could be involved in the regulation of the use of fatty acids as fuel substrates, the UCP-3 induction achieved after bezafibrate and Wy-14, 643 treatment may indicate a higher oxidation of fatty acids, limiting their availability to be stored as triglycerides. This change may result in a reduced rate of conversion of preadipocytes to adipocytes, which directly affects fat depots.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects*
  • Adipocytes / metabolism*
  • Animals
  • Base Sequence
  • Bezafibrate / pharmacology*
  • Carrier Proteins / genetics*
  • Cells, Cultured
  • DNA Primers / genetics
  • Ion Channels
  • Membrane Potentials / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Proteins
  • Peroxisome Proliferators / pharmacology
  • Pyrimidines / pharmacology*
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism*
  • Rats
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Transcription Factors / metabolism*
  • Uncoupling Protein 3

Substances

  • Carrier Proteins
  • DNA Primers
  • Ion Channels
  • Mitochondrial Proteins
  • Peroxisome Proliferators
  • Pyrimidines
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Ucp3 protein, rat
  • Uncoupling Protein 3
  • pirinixic acid
  • Bezafibrate