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Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean.
Clapham, J C; Arch, J R; Chapman, H; Haynes, A; Lister, C; Moore, G B; Piercy, V; Carter, S A; Lehner, I; Smith, S A; Beeley, L J; Godden, R J; Herrity, N; Skehel, M; Changani, K K; Hockings, P D; Reid, D G; Squires, S M; Hatcher, J; Trail, B; Latcham, J; Rastan, S; Harper, A J; Cadenas, S; Buckingham, J A; Brand, M D; Abuin, A.
Afiliação
  • Clapham JC; Department of Vascular Biology, SmithKline Beecham Pharmaceuticals, Harlow, Essex, UK. JohnvClapham-1@sbphrd.com
Nature ; 406(6794): 415-8, 2000 Jul 27.
Article em En | MEDLINE | ID: mdl-10935638
ABSTRACT
Uncoupling protein-3 (UCP-3) is a recently identified member of the mitochondrial transporter superfamily that is expressed predominantly in skeletal muscle. 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 metabolism. 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.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Músculo Esquelético Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2000 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Músculo Esquelético Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2000 Tipo de documento: Article