
Leptin is a fat cell-derived satiety factor that regulates food intake and energy expenditure. Its effects are mediated by interactions with the leptin receptor (Ob-R) that is alternatively spliced to encode at least five isoforms(a-e), which are distributed in a wide range of tissues including the hypothalamus. Ob-R is a member of cytokine receptors and involves the JAK-STAT signal transduction system. We found Ob-R mutations in Zucker fatty rats and obese Koletsky rats and demonstrated that Ob-R dysfunction brings around hyperphagia and obesity. However we and others have not found any Ob-R mutation in human obese subjects.
Leptin, Gene Expression, Proteins, Receptors, Cell Surface, Hyperphagia, Protein-Tyrosine Kinases, Rats, Rats, Zucker, Mice, Mutation, Trans-Activators, Animals, Humans, Receptors, Leptin, Obesity, Carrier Proteins, Signal Transduction
Leptin, Gene Expression, Proteins, Receptors, Cell Surface, Hyperphagia, Protein-Tyrosine Kinases, Rats, Rats, Zucker, Mice, Mutation, Trans-Activators, Animals, Humans, Receptors, Leptin, Obesity, Carrier Proteins, Signal Transduction
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