Evidence map›Paper›PMID 34462441›Full record

ArticleNature communications2021

A nutrient-responsive hormonal circuit mediates an inter-tissue program regulating metabolic homeostasis in adult Drosophila.

Takashi Koyama, Selim Terhzaz, Muhammad T Naseem, Stanislav Nagy, Kim Rewitz, Julian A T Dow, Shireen A Davies, Kenneth V Halberg

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 60 citations in OpenAlex.

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  9. Stress-induced organismal death is genetically regulated by the mTOR-Zeste-Phae1 axis.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  20. Self-DNA Inhibition inBiology · 2023
    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 at 3 institutions in 2 countries.

Takashi Koyama *Section for Cell and Neurobiology, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-4203-114X
Selim Terhzaz *Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-6192-6558
Muhammad T NaseemSection for Cell and Neurobiology, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-6225-9777
Stanislav NagySection for Cell and Neurobiology, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark.
Kim RewitzSection for Cell and Neurobiology, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-4409-9941
Julian A T DowInstitute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-9595-5146
Shireen A DaviesInstitute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Kenneth V HalbergSection for Cell and Neurobiology, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark. kahalberg@bio.ku.dk.ORCID http://orcid.org/0000-0002-5903-7196
University of Copenhagen · DKUniversity of Glasgow · GBMRC University of Glasgow Centre for Virus Research · GB

Funding

Biotechnology and Biological Sciences Research Council BB/P008097/1Medical Research Council MC_UU_12014/8
6 · The paper itself

Abstract

Animals maintain metabolic homeostasis by modulating the activity of specialized organs that adjust internal metabolism to external conditions. However, the hormonal signals coordinating these functions are incompletely characterized. Here we show that six neurosecretory cells in the Drosophila central nervous system respond to circulating nutrient levels by releasing Capa hormones, homologs of mammalian neuromedin U, which activate the Capa receptor (CapaR) in peripheral tissues to control energy homeostasis. Loss of Capa/CapaR signaling causes intestinal hypomotility and impaired nutrient absorption, which gradually deplete internal nutrient stores and reduce organismal lifespan. Conversely, increased Capa/CapaR activity increases fluid and waste excretion. Furthermore, Capa/CapaR inhibits the release of glucagon-like adipokinetic hormone from the corpora cardiaca, which restricts energy mobilization from adipose tissue to avoid harmful hyperglycemia. Our results suggest that the Capa/CapaR circuit occupies a central node in a homeostatic program that facilitates the digestion and absorption of nutrients and regulates systemic energy balance.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsEnergy MetabolismFemaleHomeostasisInsect HormonesLongevityMaleNeuropeptidesNutrientsOligopeptidesPyrrolidonecarboxylic AcidReceptors, G-Protein-CoupledSignal Transductionadipokinetic hormonecapa protein, DrosophilaCapaR protein, DrosophilaDrosophila ProteinsInsect HormonesNeuropeptidesNutrientsOligopeptidesPyrrolidonecarboxylic AcidReceptors, G-Protein-Coupled

Identifiers

PMID34462441
PMCPMC8405823
OpenAlexW3196787022

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.