Evidence map›Paper›PMID 31153646›Full record

ArticleNeuron2019

Temporally and Spatially Distinct Thirst Satiation Signals.

Vineet Augustine, Haruka Ebisu, Yuan Zhao, Sangjun Lee, Brittany Ho, Grace O Mizuno, Lin Tian, Yuki Oka

Abstract read
In one paragraph

Article in Neuron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Review
  7. Review
  8. A Poly(methacrolein-Nanomaterials (Basel, Switzerland) · 2025
    Article
  9. Body fluid regulation.Current opinion in neurobiology · 2025
    Review
  10. Review
  11. Review
  12. Dysregulation of the fluid homeostasis system by aging.bioRxiv : the preprint server for biology · 2024
    Article
  13. The cerebellum modulates thirst.Nature neuroscience · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Vineet AugustineDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Haruka EbisuDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Yuan ZhaoDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Sangjun LeeDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Brittany HoDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Grace O MizunoDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Davis, CA 95616, USA.
Lin TianDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Davis, CA 95616, USA.
Yuki OkaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA. Electronic address: yoka@caltech.edu.

Funding

Neural circuits underlying thirst and satiety regulationR01NS109997 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI OKA, YUKI · 2018 to 2022
$1.9M
Genetic dissection of the neural circuits regulating appetiteR56MH113030 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI OKA, YUKI · 2017 to 2018
$825k
NIMH NIH HHS R56 MH113030NINDS NIH HHS R01 NS109997
6 · The paper itself

Abstract

For thirsty animals, fluid intake provides both satiation and pleasure of drinking. How the brain processes these factors is currently unknown. Here, we identified neural circuits underlying thirst satiation and examined their contribution to reward signals. We show that thirst-driving neurons receive temporally distinct satiation signals by liquid-gulping-induced oropharyngeal stimuli and gut osmolality sensing. We demonstrate that individual thirst satiation signals are mediated by anatomically distinct inhibitory neural circuits in the lamina terminalis. Moreover, we used an ultrafast dopamine (DA) sensor to examine whether thirst satiation itself stimulates the reward-related circuits. Interestingly, spontaneous drinking behavior but not thirst drive reduction triggered DA release. Importantly, chemogenetic stimulation of thirst satiation neurons did not activate DA neurons under water-restricted conditions. Together, this study dissected the thirst satiation circuit, the activity of which is functionally separable from reward-related brain activity.

Indexed as

AnimalsCalciumDopamineDrinkingFemaleGABAergic NeuronsGlucagon-Like Peptide 1Luminescent ProteinsMaleMiceMice, Inbred C57BLMice, TransgenicNerve NetNeural PathwaysNitric Oxide Synthase Type IOptogeneticsCalciumDopamineGlucagon-Like Peptide 1glucagon-like peptide 1 (7-37)Luminescent ProteinsNitric Oxide Synthase Type IPeptide Fragmentsappetitegut-brain axishomeostasisreward circuitsatiationthirst

Identifiers

PMID31153646
PMCPMC7335596

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.