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

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作者
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 J. Godden
Nicole Herrity
Mark Skehel
K. Kumar Changani
Paul D. Hockings
David G. Reid
Sarah M. Squires
Jonathan Hatcher
Brenda Trail
Judy Latcham
Sohaila Rastan
Alexander J. Harper
Susana Cadenas
Julie A. Buckingham
Martin D. Brand
Alejandro Abuin
机构
[1] Departments of Vascular Biology,Comparative Genetics
[2] Bioinformatics,Department of Biochemistry
[3] Molecular Biology,Target Genomics
[4] Gene Expression Sciences,undefined
[5] Bioanalytical Sciences,undefined
[6] Neurobehavioiural Research,undefined
[7] SmithKline Beecham Pharmaceuticals,undefined
[8] Departments of Safety Assessment,undefined
[9] Laboratory Animal Sciences,undefined
[10] University of Cambridge,undefined
[11] MRC-Dunn Human Nutrition Unit,undefined
[12] Lexicon Genetics,undefined
[13] Pfizer Ltd,undefined
来源
Nature | 2000年 / 406卷
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摘要
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.
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页码:415 / 418
页数:3
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