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Am J Physiol Endocrinol Metab ; 279(2): E293-300, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10913028

ABSTRACT

Nonshivering thermogenesis induced in brown adipose tissue (BAT) during high-fat feeding is mediated through uncoupling protein 1 (UCP1). UCP2 is a recently identified homologue found in many tissues. To determine the role of UCP1 and UCP2 in thermoregulation and energy balance, we investigated the long-term effect of high-fat feeding on mRNA levels in mice at two different ambient temperatures. We also treated mice with the anorectic peptide enterostatin and compared mRNA levels in BAT, white adipose tissue (WAT), stomach, and duodenum. Here, we report that high-fat feeding at 23 degrees C increased UCP1 and UCP2 levels in BAT four- and threefold, respectively, and increased UCP2 levels fourfold in WAT. However, at 29 degrees C, UCP1 decreased, whereas UCP2 remained unchanged in BAT and increased twofold in WAT. Enterostatin increased UCP1 and decreased UCP2 mRNA in BAT. In stomach and duodenum, high-fat feeding decreased UCP2 mRNA, whereas enterostatin increased it. Our results suggest that the regulation of uncoupling protein mRNA levels by high-fat feeding is dependent on ambient temperature and that enterostatin is able to modulate it.


Subject(s)
Carrier Proteins/genetics , Colipases/pharmacology , Dietary Fats/metabolism , Gene Expression/drug effects , Membrane Proteins/genetics , Membrane Transport Proteins , Mitochondrial Proteins , Protein Precursors/pharmacology , Proteins/genetics , Temperature , Adipose Tissue/metabolism , Adipose Tissue, Brown/metabolism , Animals , Blood Glucose/drug effects , Body Weight/drug effects , Carrier Proteins/biosynthesis , Colipases/metabolism , Dietary Fats/pharmacology , Duodenum/metabolism , Eating/drug effects , Enzyme Precursors , Gastric Mucosa/metabolism , Glucose Tolerance Test , Ion Channels , Lipase/metabolism , Male , Membrane Proteins/biosynthesis , Mice , Mice, Inbred Strains , Pancreas/drug effects , Pancreas/enzymology , Protein Biosynthesis , RNA, Messenger/biosynthesis , Uncoupling Protein 1 , Uncoupling Protein 2
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