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      AdipoR1 mediates the anorexigenic and insulin/leptin-like actions of adiponectin in the hypothalamus.

      Febs Letters
      Adaptor Proteins, Signal Transducing, metabolism, Adiponectin, pharmacology, physiology, Animals, Anorexia, chemically induced, Arcuate Nucleus of Hypothalamus, drug effects, Carrier Proteins, Eating, Forkhead Transcription Factors, Hypothalamic Area, Lateral, Insulin, Insulin Receptor Substrate Proteins, Intracellular Signaling Peptides and Proteins, Janus Kinase 2, Leptin, Male, Nerve Tissue Proteins, Neurons, Phosphoproteins, Proto-Oncogene Proteins c-akt, RNA, Antisense, genetics, Rats, Rats, Wistar, Receptors, Adiponectin, STAT3 Transcription Factor, Signal Transduction

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          Abstract

          Adiponectin exerts an insulin-sensitizing effect, improving insulin action in peripheral tissues and restraining insulin resistance. Here, we explore the hypothesis that adiponectin can reproduce some of the actions of insulin/leptin in the hypothalamus. The presence of AdipoR1 and AdipoR2 was mapped to the arcuate and lateral hypothalamic nuclei. Icv adiponectin reduced food intake, which was accompanied by activation/engagement of IRS1/2, ERK, Akt, FOXO1, JAK2 and STAT3. All these actions were dependent on AdipoR1, since inhibition of this receptor, and not of AdipoR2, completely reversed the effects described above. Thus, adiponectin acts in the hypothalamus, activating elements of the canonical insulin and leptin signaling pathways and promoting reduction of food intake.

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