4.8 Article

A gut-to-brain signal of fluid osmolarity controls thirst satiation

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NATURE
卷 568, 期 7750, 页码 98-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41586-019-1066-x

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资金

  1. NSF Graduate Research Fellowship [DGE-1144247]
  2. UCSF Discovery Fellowship
  3. Genentech Foundation Predoctoral Fellowship
  4. NIH National Research Service Award [F31-HL137383]
  5. New York Stem Cell Foundation
  6. Pathway Award from the American Diabetes Association
  7. Rita Allen Foundation
  8. McKnight Foundation
  9. Alfred P. Sloan Foundation
  10. Brain and Behavior Research Foundation
  11. Esther A. and Joseph Klingenstein Foundation
  12. UCSF Program for Breakthrough Biomedical Research
  13. UCSF Nutrition Obesity Research Center [DK0908722]
  14. NIH New Innovator Award [DP2-DK109533, R01-DK106399, R01-NS094781]

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Satiation is the process by which eating and drinking reduce appetite. For thirst, oropharyngeal cues have a critical role in driving satiation by reporting to the brain the volume of fluid that has been ingested(1-12). By contrast, the mechanisms that relay the osmolarity of ingested fluids remain poorly understood. Here we show that the water and salt content of the gastrointestinal tract are precisely measured and then rapidly communicated to the brain to control drinking behaviour in mice. We demonstrate that this osmosensory signal is necessary and sufficient for satiation during normal drinking, involves the vagus nerve and is transmitted to key forebrain neurons that control thirst and vasopressin secretion. Using microendoscopic imaging, we show that individual neurons compute homeostatic need by integrating this gastrointestinal osmosensory information with oropharyngeal and blood-borne signals. These findings reveal how the fluid homeostasis system monitors the osmolarity of ingested fluids to dynamically control drinking behaviour.

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