Evidence map›Paper›PMID 20534837›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

The monoaminergic modulation of sensory-mediated aversive responses in Caenorhabditis elegans requires glutamatergic/peptidergic cotransmission.

Gareth Harris, Holly Mills, Rachel Wragg, Vera Hapiak, Michelle Castelletto, Amanda Korchnak, Richard W Komuniecki

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

55 citing papers in PubMed, 82 citations in OpenAlex.

  1. Advances in drug addiction research usingFrontiers in cell and developmental biology · 2026
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  4. Glial KCNQ KNeuron · 2024
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  6. Multiple Subthreshold GPCR Signals Combined by the G-Proteins GαThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  7. Article
  8. A glial ClC ClNeuron · 2022
    Article
  9. Article
  10. Reduced CaFrontiers in neuroscience · 2022
    Article
  11. Article
  12. Article
  13. Behavioral States.Genetics · 2020
    Review
  14. Article
  15. Serotonergic modulation across sensory modalities.Journal of neurophysiology · 2020
    Review
  16. Article
  17. Article
  18. Review
  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

7 authors at 1 institution in 1 country.

Gareth HarrisDepartment of Biological Sciences, University of Toledo, Toledo, Ohio 43606-3390, USA.
Holly Mills
Rachel Wragg
Vera Hapiak
Michelle Castelletto
Amanda Korchnak
Richard W Komuniecki
University of Toledo · US

Funding

Regulation of T cell responses by P2RX7R01AI145147 · NIAID · UNIVERSITY OF MINNESOTA · PI JAMESON, STEPHEN C · 2019 to 2023
$3.3M
Locomotion in Parasitic NematodesR01AI072644 · NIAID · UNIVERSITY OF TOLEDO · PI KOMUNIECKI, RICHARD WALTER · 2008 to 2012
$1.6M
NIAID NIH HHS AI-145147NIAID NIH HHS R01 AI072644NIAID NIH HHS R01 AI145147
6 · The paper itself

Abstract

Monoamines and neuropeptides interact to modulate behavioral plasticity in both vertebrates and invertebrates. In Caenorhabditis elegans behavioral state or "mood" is dependent on food availability and is translated by both monoaminergic and peptidergic signaling in the fine-tuning of most behaviors. In the present study, we have examined the interaction of monoamines and peptides on C. elegans aversive behavior mediated by a pair of polymodal, nociceptive, ASH sensory neurons. Food or serotonin sensitize the ASHs and stimulate aversive responses through a pathway requiring the release of nlp-3-encoded neuropeptides from the ASHs. Peptides encoded by nlp-3 appear to stimulate ASH-mediated aversive behavior through the neuropeptide receptor-17 (NPR-17) receptor. nlp-3- and npr-17-null animals exhibit identical phenotypes and animals overexpressing either nlp-3 or npr-17 exhibit elevated aversive responses off food that are absent when nlp-3 or npr-17 are overexpressed in npr-17- or nlp-3-null animals, respectively. ASH-mediated aversive responses are increased by activating either Galpha(q) or Galpha(s) in the ASHs, with Galpha(s) signaling specifically stimulating the release of nlp-3-encoded peptides. In contrast, octopamine appears to inhibit 5-HT stimulation by activating Galpha(o) signaling in the ASHs that, in turn, inhibits both Galpha(s) and Galpha(q) signaling and the release of nlp-3-encoded peptides. These results demonstrate that serotonin and octopamine reversibly modulate the activity of the ASHs, and highlight the utility of the C. elegans model for defining interactions between monoamines and peptides in individual neurons of complex sensory-mediated circuits.

Indexed as

AnimalsAvoidance LearningBiogenic MonoaminesCaenorhabditis elegansCaenorhabditis elegans ProteinsGTP-Binding Protein alpha Subunits, Gq-G11GTP-Binding Protein alpha Subunits, GsNeuropeptidesNociceptorsOctanolsOctopamineSerotoninSignal TransductionBiogenic MonoaminesCaenorhabditis elegans ProteinsGTP-Binding Protein alpha Subunits, Gq-G11GTP-Binding Protein alpha Subunits, GsNeuropeptidesOctanolsOctopamineSerotonin

Identifiers

PMID20534837
PMCPMC3005568
OpenAlexW1989512833

What OpenQuestion holds

Textmetadata
LicenceTDM
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.