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      Modulation of insulin activities by leptin.

      Science (New York, N.Y.)
      Adaptor Proteins, Signal Transducing, Carrier Proteins, genetics, metabolism, Cell Line, Down-Regulation, drug effects, GRB2 Adaptor Protein, Gene Expression Regulation, Enzymologic, Gluconeogenesis, Glucose, Humans, Insulin, pharmacology, Insulin Antagonists, Insulin Receptor Substrate Proteins, Leptin, Liver, cytology, Phosphatidylinositol 3-Kinases, Phosphoenolpyruvate Carboxykinase (GTP), Phosphoproteins, Phosphorylation, Phosphotransferases (Alcohol Group Acceptor), Phosphotyrosine, Proteins, Receptor, Epidermal Growth Factor, Receptor, Insulin, Receptors, Cell Surface, Receptors, Leptin, Signal Transduction, Tumor Cells, Cultured

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          Abstract

          Leptin mediates its effects on food intake through the hypothalamic form of its receptor OB-R. Variants of OB-R are found in other tissues, but their function is unknown. Here, an OB-R variant was found in human hepatic cells. Exposure of these cells to leptin, at concentrations comparable with those present in obese individuals, caused attenuation of several insulin-induced activities, including tyrosine phosphorylation of the insulin receptor substrate-1 (IRS-1), association of the adapter molecule growth factor receptor-bound protein 2 with IRS-1, and down-regulation of gluconeogenesis. In contrast, leptin increased the activity of IRS-1-associated phosphatidylinositol 3-kinase. These in vitro studies raise the possibility that leptin modulates insulin activities in obese individuals.

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