Bidirectional regulation of uncoupling protein-3 and GLUT-4 mRNA in skeletal muscle by cold

Am J Physiol. 1998 Sep;275(3):E386-91. doi: 10.1152/ajpendo.1998.275.3.E386.

Abstract

To elucidate the possible role of the mitochondrial uncoupling protein (UCP)-3 in skeletal muscle as a regulator of adaptive thermogenesis and energy balance, we examined the modulation by cold exposure (5 degrees C) of UCP-3 and glucose transporter isoform GLUT-4 mRNAs in male Sprague-Dawley rats. In skeletal muscle, UCP-3 and GLUT-4 mRNAs increased two- to threefold between 6 and 24 h of cold exposure and then decreased to 50% of the control value after 6 days in the cold. In contrast, skeletal muscle UCP-2 mRNA showed a small increase on day 3 and returned to normal after 6 days. The bidirectional regulation of UCP-3 and GLUT-4 mRNAs in skeletal muscle by cold suggests that UCP-3 may be a major mediator of acute adaptive thermogenesis but then is downregulated, along with GLUT-4, in the chronic state to preserve energy. In contrast, cold exposure caused only transient changes of UCP-2 and GLUT-4 mRNA in heart. These data are consistent with the necessity of the heart to continuously expend energy to maintain blood circulation, regardless of environmental conditions.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acclimatization / physiology*
  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Cloning, Molecular
  • Cold Temperature
  • Gene Expression Regulation / physiology*
  • Glucose Transporter Type 4
  • Humans
  • Interleukin 1 Receptor Antagonist Protein
  • Ion Channels
  • Male
  • Membrane Transport Proteins*
  • Mitochondria / metabolism
  • Mitochondria, Muscle / metabolism
  • Mitochondrial Proteins*
  • Monosaccharide Transport Proteins / biosynthesis
  • Monosaccharide Transport Proteins / genetics*
  • Muscle Proteins*
  • Muscle, Skeletal / physiology*
  • Organ Specificity
  • Polymerase Chain Reaction
  • Protein Biosynthesis
  • Proteins / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / biosynthesis
  • Sialoglycoproteins / biosynthesis
  • Sialoglycoproteins / genetics
  • Uncoupling Protein 2
  • Uncoupling Protein 3

Substances

  • Carrier Proteins
  • Glucose Transporter Type 4
  • IL1RN protein, human
  • Interleukin 1 Receptor Antagonist Protein
  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Proteins
  • Recombinant Proteins
  • SLC2A4 protein, human
  • Sialoglycoproteins
  • Slc2a4 protein, rat
  • UCP2 protein, human
  • UCP3 protein, human
  • Ucp2 protein, rat
  • Ucp3 protein, rat
  • Uncoupling Protein 2
  • Uncoupling Protein 3