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Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean

Author

Listed:
  • John C. Clapham

    (Departments of Vascular Biology)

  • Jonathan R. S. Arch

    (Departments of Vascular Biology)

  • Helen Chapman

    (Departments of Vascular Biology)

  • Andrea Haynes

    (Departments of Vascular Biology)

  • Carolyn Lister

    (Departments of Vascular Biology)

  • Gary B. T. Moore

    (Departments of Vascular Biology)

  • Valerie Piercy

    (Departments of Vascular Biology)

  • Sabrina A. Carter

    (Departments of Vascular Biology)

  • Ines Lehner

    (Departments of Vascular Biology)

  • Stephen A. Smith

    (Departments of Vascular Biology)

  • Lee J. Beeley

    (Bioinformatics
    Pfizer Ltd)

  • Robert J. Godden

    (Molecular Biology)

  • Nicole Herrity

    (Gene Expression Sciences)

  • Mark Skehel

    (Bioanalytical Sciences)

  • K. Kumar Changani

    (Departments of Safety Assessment)

  • Paul D. Hockings

    (Departments of Safety Assessment)

  • David G. Reid

    (Departments of Safety Assessment)

  • Sarah M. Squires

    (Departments of Safety Assessment)

  • Jonathan Hatcher

    (Neurobehavioiural Research)

  • Brenda Trail

    (Neurobehavioiural Research)

  • Judy Latcham

    (Laboratory Animal Sciences)

  • Sohaila Rastan

    (SmithKline Beecham Pharmaceuticals)

  • Alexander J. Harper

    (Neurobehavioiural Research)

  • Susana Cadenas

    (University of Cambridge
    MRC-Dunn Human Nutrition Unit)

  • Julie A. Buckingham

    (University of Cambridge
    MRC-Dunn Human Nutrition Unit)

  • Martin D. Brand

    (University of Cambridge
    MRC-Dunn Human Nutrition Unit)

  • Alejandro Abuin

    (SmithKline Beecham Pharmaceuticals
    Lexicon Genetics)

Abstract

Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily1,2 that is expressed predominantly in skeletal muscle1,2. However, its close relative UCP-1 is expressed exclusively in brown adipose tissue, a tissue whose main function is fat combustion and thermogenesis. Studies on the expression of UCP-3 in animals and humans in different physiological situations support a role for UCP-3 in energy balance and lipid metabolism3,4. However, direct evidence for these roles is lacking. Here we describe the creation of transgenic mice that overexpress human UCP-3 in skeletal muscle. These mice are hyperphagic but weigh less than their wild-type littermates. Magnetic resonance imaging shows a striking reduction in adipose tissue mass. The mice also exhibit lower fasting plasma glucose and insulin levels and an increased glucose clearance rate. This provides evidence that skeletal muscle UCP-3 has the potential to influence metabolic rate and glucose homeostasis in the whole animal.

Suggested Citation

  • John C. Clapham & Jonathan R. S. Arch & Helen Chapman & Andrea Haynes & Carolyn Lister & Gary B. T. Moore & Valerie Piercy & Sabrina A. Carter & Ines Lehner & Stephen A. Smith & Lee J. Beeley & Robert, 2000. "Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean," Nature, Nature, vol. 406(6794), pages 415-418, July.
  • Handle: RePEc:nat:nature:v:406:y:2000:i:6794:d:10.1038_35019082
    DOI: 10.1038/35019082
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