Brown fat is essential for cold-induced thermogenesis but not for obesity resistance in aP2-Ucp mice
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Energy Metabolism MeSH
- Adipose Tissue, Brown physiology MeSH
- Homozygote MeSH
- Ion Channels MeSH
- Membrane Proteins genetics physiology MeSH
- Membrane Transport Proteins * MeSH
- Mitochondrial Proteins * MeSH
- Mice, Inbred C57BL MeSH
- Mice, Transgenic MeSH
- Mice MeSH
- Cold Temperature * MeSH
- Obesity genetics physiopathology MeSH
- Immunity, Innate genetics MeSH
- Promoter Regions, Genetic MeSH
- Proteins genetics physiology MeSH
- Thyroid Gland physiology MeSH
- Body Weight MeSH
- Body Temperature Regulation genetics physiology MeSH
- Transgenes MeSH
- Carrier Proteins genetics physiology MeSH
- Adipose Tissue physiology MeSH
- Uncoupling Protein 1 MeSH
- Uncoupling Protein 2 MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ion Channels MeSH
- Membrane Proteins MeSH
- Membrane Transport Proteins * MeSH
- Mitochondrial Proteins * MeSH
- Proteins MeSH
- Carrier Proteins MeSH
- Ucp1 protein, mouse MeSH Browser
- Uncoupling Protein 1 MeSH
- Uncoupling Protein 2 MeSH
The role of brown adipose tissue in total energy balance and cold-induced thermogenesis was studied. Mice expressing mitochondrial uncoupling protein 1 (UCP-1) from the fat-specific aP2 gene promoter (heterozygous and homozygous aP2-Ucp transgenic mice) and their nontransgenic C57BL6/J littermates were used. The transgenic animals are resistant to obesity induced by a high-fat diet, presumably due to ectopic synthesis of UCP-1 in white fat. These animals exhibited atrophy of brown adipose tissue, as indicated by smaller size of brown fat and reduction of its total UCP-1 and DNA contents. Norepinephrine-induced respiration (measured in pentobarbital sodium-anesthetized animals) was decreased proportionally to the dosage of the transgene, and the homozygous (but not heterozygous) transgenic mice exhibited a reduction in their capacity to maintain body temperature in the cold. Our results indicate that the role of brown fat in cold-induced thermogenesis cannot be substituted by increased energy expenditure in other tissues.
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