Evidence map›Paper›PMID 32292064›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2020

A novel regulator of thirst behavior: phoenixin.

Christopher J Haddock, Gislaine Almeida-Pereira, Lauren M Stein, Gina L C Yosten, Willis K Samson

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Premetazoan Origin of Neuropeptide Signaling.Molecular biology and evolution · 2022
    Article
  7. Review
  8. Regulation and physiological functions of phoenixin.Frontiers in molecular biosciences · 2022
    Review
  9. Article
  10. Phoenixin: More than Reproductive Peptide.International journal of molecular sciences · 2020
    Review
  11. American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  12. 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

5 authors at 1 institution in 1 country.

Christopher J HaddockDepartment of Pharmacology and Physiology, Center for Neuroscience Research, Saint Louis University School of Medicine, St. Louis, Missouri.
Gislaine Almeida-PereiraDepartment of Pharmacology and Physiology, Center for Neuroscience Research, Saint Louis University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-3967-5115
Lauren M SteinDepartment of Pharmacology and Physiology, Center for Neuroscience Research, Saint Louis University School of Medicine, St. Louis, Missouri.
Gina L C YostenDepartment of Pharmacology and Physiology, Center for Neuroscience Research, Saint Louis University School of Medicine, St. Louis, Missouri.
Willis K SamsonDepartment of Pharmacology and Physiology, Center for Neuroscience Research, Saint Louis University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-0560-4447
Saint Louis University · US

Funding

Angiotensin Receptor Regulation By Upstream Short Open Reading FramesR01HL121456 · NHLBI · GEORGETOWN UNIVERSITY · PI SAMSON, WILLIS K., SANDBERG, KATHRYN L · 2014 to 2017
$3.1M
Integrative Physiology of Obesity: Role of GPR160R01DK118340 · NIDDK · SAINT LOUIS UNIVERSITY · PI YOSTEN, GINA L.C. · 2018 to 2022
$2.3M
HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI) HL121456HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK118340NHLBI NIH HHS R01 HL121456NIDDK NIH HHS R01 DK118340
6 · The paper itself

Abstract

There are examples of physiological conditions under which thirst is inappropriately exaggerated, and the mechanisms for these paradoxical ingestive behaviors remain unknown. We are interested in thirst mechanisms across the female life cycle and have identified a novel mechanism through which ingestive behavior may be activated. We discovered a previously unrecognized endogenous hypothalamic peptide, phoenixin (PNX), identified physiologically relevant actions of the peptide in brain and pituitary gland to control reproductive hormone secretion in female rodents, and in the process identified the previously orphaned G protein-coupled receptor Gpr173 to be a potential receptor for the peptide. Labeled PNX binding distribution in brain parallels areas known to be important in ingestive behaviors as well in areas where gonadal steroids feedback to control estrous cyclicity (Stein LM, Tullock CW, Mathews SK, Garcia-Galiano D, Elias CF, Samson WK, Yosten GLC,

Indexed as

AnimalsDrinking BehaviorEstrous CycleFemaleHomeostasisHypothalamusMalePeptide HormonesRatsRats, Sprague-DawleyReceptors, G-Protein-CoupledRNA, Small InterferingThirstgpr173 protein, ratPeptide HormonesphoenixinReceptors, G-Protein-CoupledRNA, Small Interferingangiotensin IIfluid and electrolyte homeostasisphoenixinsalt appetitethirst

Identifiers

PMID32292064
PMCPMC7311681
OpenAlexW3015242861

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.