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      Dynamics of gut-brain communication underlying hunger

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          Summary

          Communication between the gut and brain is critical for homeostasis, but how this communication is represented in the dynamics of feeding circuits is unknown. Here we describe nutritional regulation of key neurons that control hunger in vivo. We show that intragastric nutrient infusion rapidly and durably inhibits hunger-promoting AgRP neurons in awake, behaving mice. This inhibition is proportional to the number of calories infused but surprisingly independent of macronutrient identity or nutritional state. We show that three gastrointestinal signals – serotonin, CCK, and PYY – are necessary or sufficient for these effects. In contrast, the hormone leptin has no acute effect on dynamics of these circuits or their sensory regulation, but instead induces a slow modulation that develops over hours and is required for inhibition of feeding. These findings reveal how layers of visceral signals operating on distinct timescales converge on hypothalamic feeding circuits to generate a central representation of energy balance.

          Graphical abstract

          Beutler et al. reveal how nutritional signals regulate the hypothalamic hunger circuit. They show that intragastric nutrients inhibit AgRP neurons rapidly in a way dependent solely on calorie content, whereas the satiety hormone leptin only acts on timescale of hours.

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          Author and article information

          Journal
          8809320
          1600
          Neuron
          Neuron
          Neuron
          0896-6273
          1097-4199
          15 October 2017
          11 October 2017
          11 October 2018
          : 96
          : 2
          : 461-475.e5
          Affiliations
          [1 ]Department of Physiology, University of California, San Francisco, San Francisco, CA 94158
          [2 ]Department of Medicine, University of California, San Francisco, San Francisco, CA 94158
          [3 ]Kavli Center for Fundamental Neuroscience, University of California, San Francisco, San Francisco, CA 94158
          [4 ]Neuroscience Graduate Program, University of California, San Francisco, San Francisco, CA 94158
          Author notes
          [*]

          equal contributions

          Article
          PMC5691364 PMC5691364 5691364 nihpa910094
          10.1016/j.neuron.2017.09.043
          5691364
          29024666
          6a24f002-1a70-43a4-8aee-6ed2c802417a
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