Evidence map›Paper›PMID 28448025›Full record

ArticleJournal of visualized experiments : JoVE2017

Novel Assay for Cold Nociception in Drosophila Larvae.

Heather N Turner, Christian Landry, Michael J Galko

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Nociception in fruit fly larvae.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  2. Frontiers in physiology · 2022
    Review
  3. 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

3 authors.

Heather N TurnerDepartment of Genetics, UT MD Anderson Cancer Center; Neuroscience Program, Graduate School of Biomedical Sciences at Houston; Section of Neurobiology, University of Southern California.
Christian LandryProDev Engineering.
Michael J GalkoDepartment of Genetics, UT MD Anderson Cancer Center; Neuroscience Program, Graduate School of Biomedical Sciences at Houston; Genes and Development Program, Graduate School of Biomedical Sciences at Houston; mjgalko@mdanderson.org.

Funding

A genetically tractable model of tissue damage-induced nociceptive sensitizationR01NS069828 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GALKO, MICHAEL J · 2010 to 2013
$1.1M
Development of a mechanical nociceptive sensitization model in DrosophilaR21NS087360 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GALKO, MICHAEL J · 2014 to 2015
$440k
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
NINDS NIH HHS F31 NS083306NINDS NIH HHS R01 NS069828NINDS NIH HHS R21 NS087360
6 · The paper itself

Abstract

How organisms sense and respond to noxious temperatures is still poorly understood. Further, the mechanisms underlying sensitization of the sensory machinery, such as in patients experiencing peripheral neuropathy or injury-induced sensitization, are not well characterized. The genetically tractable Drosophila model has been used to study the cells and genes required for noxious heat detection, which has yielded multiple conserved genes of interest. Little is known however about the cells and receptors important for noxious cold sensing. Although, Drosophila does not survive prolonged exposure to cold temperatures (≤10 ºC), and will avoid cool, preferring warmer temperatures in behavioral preference assays, how they sense and possibly avoid noxious cold stimuli has only recently been investigated. Here we describe and characterize the first noxious cold (≤10 ºC) behavioral assay in Drosophila. Using this tool and assay, we show an investigator how to qualitatively and quantitatively assess cold nociceptive behaviors. This can be done under normal/healthy culture conditions, or presumably in the context of disease, injury or sensitization. Further, this assay can be applied to larvae selected for desired genotypes, which might impact thermosensation, pain, or nociceptive sensitization. Given that pain is a highly conserved process, using this assay to further study thermal nociception will likely glean important understanding of pain processes in other species, including vertebrates.

Indexed as

NociceptionThermosensingAnimalsBiological AssayCold TemperatureDrosophilaDrosophila ProteinsHumansLarvaMaleDrosophila Proteins

Identifiers

PMID28448025
PMCPMC5564461

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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.