Evidence map›Paper›PMID 30586392›Full record

ArticlePloS one2018

Injury-induced cold sensitization in Drosophila larvae involves behavioral shifts that require the TRP channel Brv1.

Heather N Turner, Atit A Patel, Daniel N Cox, Michael J Galko

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Nociception in fruit fly larvae.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  5. Review
  6. Article
  7. Transient and Steady-State Properties ofFrontiers in cellular neuroscience · 2022
    Article
  8. Article
  9. Article
  10. From wound response to repair - lessons from C. elegans.Cell regeneration (London, England) · 2021
    Review
  11. Article
  12. Article
  13. An assay for chemical nociception inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  14. PeripheralPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  15. 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

4 authors.

Heather N TurnerDepartment of Genetics, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.ORCID 0000-0002-5819-5600
Atit A PatelNeuroscience Institute, Georgia State University, Atlanta, Georgia, United States of America.
Daniel N CoxNeuroscience Institute, Georgia State University, Atlanta, Georgia, United States of America.
Michael J GalkoDepartment of Genetics, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.ORCID 0000-0002-3759-2017

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI KEVIN R COOK · 2014 to 2026
$13.5M
The molecular and genetic bases of diverse tissue repair responses in postembryonic DrosophilaR35GM126929 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GALKO, MICHAEL J · 2018 to 2025
$3.4M
Cytoskeletal mechanisms of dendrite arbor shape developmentR01NS086082 · NINDS · GEORGIA STATE UNIVERSITY · PI ASCOLI, GIORGIO A, COX, DANIEL N · 2013 to 2023
$3.1M
Dissecting the Molecular Mechanisms of Cold Nociception in Drosophila LarvaeF31NS083306 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TURNER, HEATHER NICOLE · 2013 to 2014
$38k
NIGMS NIH HHS R35 GM126929NIH HHS P40 OD018537NINDS NIH HHS F31 NS083306
6 · The paper itself

Abstract

Nociceptive sensitization involves an increase in responsiveness of pain sensing neurons to sensory stimuli, typically through the lowering of their nociceptive threshold. Nociceptive sensitization is common following tissue damage, inflammation, and disease and serves to protect the affected area while it heals. Organisms can become sensitized to a range of noxious and innocuous stimuli, including thermal stimuli. The basic mechanisms underlying sensitization to warm or painfully hot stimuli have begun to be elucidated, however, sensitization to cold is not well understood. Here, we develop a Drosophila assay to study cold sensitization after UV-induced epidermal damage in larvae. Larvae respond to acute cold stimuli with a set of unique behaviors that include a contraction of the head and tail (CT) or a raising of the head and tail into a U-Shape (US). Under baseline, non-injured conditions larvae primarily produce a CT response to an acute cold (10°C) stimulus, however, we show that cold-evoked responses shift following tissue damage: CT responses decrease, US responses increase and some larvae exhibit a lateral body roll (BR) that is typically only observed in response to high temperature and noxious mechanical stimuli. At the cellular level, class III neurons are required for the decrease in CT, chordotonal neurons are required for the increase in US, and chordotonal and class IV neurons are required for the appearance of BR responses after UV. At the molecular level, we found that the transient receptor potential (TRP) channel brivido-1 (brv1) is required for these behavioral shifts. Our Drosophila model will allow us to precisely identify the genes and circuits involved in cold nociceptive sensitization.

Indexed as

AnimalsBehavior, AnimalCalcium-Binding ProteinsCold InjuryCold TemperatureDendritesDisease Models, AnimalDrosophila melanogasterDrosophila ProteinsHumansHyperalgesiaLarvaSensory Receptor CellsTransient Receptor Potential Channelsbrv1 protein, DrosophilaCalcium-Binding ProteinsDrosophila ProteinsTransient Receptor Potential Channels

Identifiers

PMID30586392
PMCPMC6306221

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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.